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Dental-derived mesenchymal stem cell sheets: a prospective tissue engineering for regenerative medicine


Stem cells transplantation is the main method of tissue engineering regeneration treatment, the viability and therapeutic efficiency are limited. Scaffold materials also play an important role in tissue engineering, whereas there are still many limitations, such as rejection and toxic side effects caused by scaffold materials. Cell sheet engineering is a scaffold-free tissue technology, which avoids the side effects of traditional scaffolds and maximizes the function of stem cells. It is increasingly being used in the field of tissue regenerative medicine. Dental-derived mesenchymal stem cells (DMSCs) are multipotent cells that exist in various dental tissues and can be used in stem cell-based therapy, which is impactful in regenerative medicine. Emerging evidences show that cell sheets derived from DMSCs have better effects in the field of regenerative medicine applications. Extracellular matrix (ECM) is the main component of cell sheets, which is a dynamic repository of signalling biological molecules and has a variety of biological functions and may play an important role in the application of cell sheets. In this review, we summarized the application status, mechanisms that sheets and ECM may play and future prospect of DMSC sheets on regeneration medicine.


DMSCs are multipotent cells that can be found in various dental tissues and have the characteristics of mesenchymal cells (MSCs). DMSCs include human dental pulp stem cells (DPSCs) [1], stem cells from human exfoliated deciduous teeth (SHED) [2], periodontal ligament stem cells (PDLSCs) [3], stem cells from the apical papilla (SCAPs) [4], gingival mesenchymal stem cells (GMSCs) [5], dental follicle stem cells (DFSCs) [6], tooth germ stem cells (TGSCs) [7] and alveolar bone-derived mesenchymal stem cells (ABMSCs) [8]. Most of them are derived from the neural crest, and have the potential of multipotent differentiation. For example, as research found that they can differentiate into adipocytes, osteocytes, chondrocytes, neurocytes, hepatocytes and pancreocytes [9]. In previous work, DMSCs presented immunomodulatory properties by secreting cytokines and developing immune receptors [10] and showed great potential capability of controlling odontogenic differentiation [11]. DMSCs are easy to culture, as they can be obtained from a wide range of sources, such as deciduous teeth, extracted orthodontic teeth or third molars, with minor damage on subjects and no ethical controversy. All above-mentioned characteristics of DMSCs make them stand out from other mesenchymal stem cells, regarding stem cell-based therapy, which is of great importance in regenerative medicine. DMSCs have been applied in some preclinical studies and clinical trials as a treatment of dental and neurodegenerative diseases, spinal cord injury, eye disease, immune diseases, orthopaedic disorders and so forth [12].

Stem cells therapy plays a therapeutic role through the three major mechanisms of stem cells differentiation, paracrine and homing. However, the limitation in cell number and getting lost easily become the major shortcomings of stem cells injection during the process. Cell sheet technology, firstly invented by Okano [13], is a unique cell delivery method with high engraftment efficiency and targeting. This technology forms the high-density cells sheet-like structures that contain only cells and their secreted ECM, which preserve cell–matrix connections, intercellular connections and specific shape provided by ECM. ECM is mainly composed of two types of secreted macromolecules: fibrous proteins and glycoproteins. These cell-associated proteins provide a certain support strength level and space filling function, regulating protein complexes, participating in cell signal transduction, and promoting cell adhesion [14]. As a scaffold-free structure, cell sheets provide a three-dimensional structure for cell proliferation and differentiation and help avoid the defects of scaffold materials that may lead to tissue inflammation or toxic reactions. In addition, cell sheets protect cells when they are digested by enzymes, which is necessary in scaffold technology [15].

In recent years, scientists have applied certain decellularized treatments to cell sheets. Decellularization technology refers to the effective removal of cellular and nuclear components, especially DNA and RNA, while retaining the essential components, biological activity and mechanical integrity of the decellularized extracellular matrix (dECM). Due to the lack of cells and the major histocompatibility complexes in dECM, the inflammatory reaction is significantly reduced, or even eliminated, in response to foreign bodies and immune rejection, while biological activity, biochemical composition, original 3D structure and mechanical integrity are highly preserved [14]. Consequently, the utilization of decellularization in regenerative medicine is on the rise. Moreover, DMSC sheets are combined with cytokines or new materials for better tissue regeneration effects, which has been utilized in many tissue regeneration processes, such as dental tissue regeneration, bone regeneration, revascularization, facial nerve regeneration and corneal regeneration.

In this review, systematic literature search was conducted for 4 databases including PubMed, Embase, Scopus, Medline. The applied search terms were broad, including synonyms, truncations and synonyms of ‘dental-derived stem cell’, ‘cell sheet’, ‘regenerative medicine’. Schematic flowchart representing study inclusion is shown in Fig. 1. Additionally, the application status, mechanisms of cell sheets and ECM, future prospect of DMSC sheets on regeneration medicine were summarized as well.

Fig. 1
figure 1

Schematic flowchart representing study inclusion

Stem cell sheets

According to existing research, stem cell sheets take the dominant place in cell sheets regenerative therapies and have been applied in periodontal ligament [16], myocardial tissue [17], cornea [18], and liver tissue [19] regeneration. During the culture and separation process, the activity and structure of the stem cell should be preserved, as well as ECM, so as to maximize the function of the cell sheets. Various methods have been developed to produce fully functioning regenerative cell sheets that can be modified or directly to different tissues.

Stem cell sheets preparation

There are three common methods to fabricate cell sheets using different surface culture dishes, namely, temperature-responsive polymer, other surface modification, as well as non-surface modification methods. First of all, the temperature-responsive polymer approach is to apply temperature-reactive polymer treatment on the surface of cell culture dishes, in which the adhesion and separation of cells are changed in different temperatures. Second, other surface modification techniques involve the application of gold-plated coatings, photoreactive materials and materials inducing reactive oxygen species (ROS) generation on the surface of the culture medium. The mature cell sheets are separated from the medium surface by an electro-reaction cell membrane separation system, light reaction system and green light-emitting diode (LED) irradiation. Lastly, non-surface modification techniques include lysozyme treatment, fibrin matrix coating, magnetic nanoparticles, and ultrasonic irradiation methods for separating cell sheets [20].

Nowadays, the most common method to synthesize DMSC sheets is to add a certain concentration of L-Ascorbic acid to the cell culture medium, since it boosts cell sheet formation by increasing the amount of ECM. After 7–14 days, the DMSC sheets can be harvested when the shrinkage at the bottom edge of the culture medium [21]. The combination of L-Ascorbic acid and temperature-responsive culture dishes is a popular method for cell sheet culture [22], as shown in Fig. 2. Beside DMSCs, the majority of bone marrow mesenchymal stem cells (BMSCs), adipose-derived stem cells (ADSCs), umbilical cord mesenchymal stem cells (UC-MSCs) and other MSC sheets are also produced through this method [23].

Fig. 2
figure 2

The origins, cell sheets preparation and decellularization of dental-derived mesenchymal stem cells (DMSCs). Dental-derived mesenchymal stem cells (DMSCs) consist of dental pulp stem cells (DPSCs), stem cells from human exfoliated deciduous teeth (SHED), periodontal ligament stem cells (PDLSCs), dental papilla stem cells (SCAPs), gingival mesenchymal stem cells (GMSCs), dental follicle stem cells (DFSCs), tooth germ stem cells (TGSCs) and alveolar bone-derived mesenchymal stem cells (ABMSCs). There are four common ways to harvest mature cell sheets: temperature-responsive polymer; other surface modification; non-surface modification methods; and adding a certain concentration of L-Ascorbic acid to the cell culture medium. The decellularized extracellular matrix (dECM) was obtained after processing to remove cells

Decellularization treatment

Due to the fact that decellularization is affected by two main factors: the methods of decellularization and tissue or cell characteristics, the decellularization scheme needs to be selected according to the specific tissue or cell characteristics, for the purpose of removing cell components, maintaining the natural ECM characteristics. All the following treatments are able to trigger decellularization: chemical, physical, enzymatic treatments and additional agents, in which chemical method uses least time. As for chemical methods, ionic or non-ionic surfactants, acids and bases, ethanol and other solvents are used to dissolve cells and decompose DNA and RNA, SDS and Triton X-100, for instance. On the other hand, enzymatic treatments usually require enzymes, such as nucleases (deoxyribonuclease and trypsin), to digest cell components. In physical treatments, the most common methods are temperature, pressure, electroporation and impact/force of mechanical agitation, slicing or mincing cells. Additional agents include tributyl phosphate (TBP), chelating agents, toxins, and supercritical carbon dioxide [14, 24, 25].

DPSC sheets applications

As a new scaffold-free material, DPSC sheets have been used in dental tissue, bone, nerve and corneal regeneration. Derived from DPSCs, DPSC sheets contain much more vascular formations, and the fibres are more porous than other dental stem cell sheets, according to previous study [26]. The single DPSC sheet was directly applied to tissue defects at the outset, with the addition of growth factors to the cell sheets during the culture process. Improved techniques were invented later on to obtain a better regeneration effect and meet the morphological needs of a variety of defects. Photobiomodulation therapy (PBMT) is the fourth element of tissue engineering, which enhances the effectiveness when applied with stem cells, growth factors, and scaffolds. PBMT is capable of increasing the fibronectin level of the ECM in DPSC sheets, resulting in tighter bonding between cells, as well as between cells and the ECM. Additionally, it probably helps the maturation of ECM, therefore increasing malleability of ECM during transplantation [21].

Dental tissue regeneration of DPSC sheets

Dental tissue regeneration can be categorized as the regeneration of dental pulp, alveolar bone, periodontal soft tissue and tooth root. As we all know, endodontic disease is one of the most common dental disease categories. Unfortunately, the current clinical treatments are likely to cause tooth reinfection or fracture. In recent years, increasing attention has been paid to the treatment of pulp regeneration of pulpless teeth. For example, the popularity of DMSCs application to mediate pulp regeneration is on the rise and validated animal models and clinical trials are also developed. Sufficient blood supply in the root canal is important during the pulp regeneration process, and therefore the vascular regeneration of the graft is a prerequisite for pulp regeneration. DPSC sheets were made into a rod-like shape, which is suitable for transplantation into root canals for a maximizing regeneration function. The three-dimensional rod-like structure enables sufficient oxygen and nutrients for DPSCs. The results from previous study showed that the outer DPSCs differentiated into odontoblast-like mineralizing cells, and pulp-like tissue, containing abundant blood vessels, was observed in the full root canal, which was similar to natural dental pulp. Conversely, no blood components were found in teeth without DPSCs constructs. Additionally, it is likely that most DPSCs within the structure had higher survival possibility, because the greater amount of ECM fibres and proteoglycan content enabled the culture medium to infiltrate better. Therefore, DPSCs had better access to oxygen, nutrients and inhibit cell apoptosis [27]. The dental pulp regeneration produced by biomimetic material with self-forming ability is a successful example in dental regenerative medicine and this material is expected to be applied in more regenerative areas closely related to angiogenesis in the near future.

Periodontitis causes progressive destruction of the periodontal support tissue, including alveolar bone resorption, attachment loss, and matrix destruction [28]. To uncover the effect of DPSCs on the treatment of periodontal regeneration, DPSCs or sheets were directly transplanted to periodontal defects in minipigs. The results presented that although new bone regeneration was observed in all groups, the bone mass of the DPSC sheets group was significantly higher than the counterpart in DPSCs injection group, which suggested a greater impact of DPSC sheets on periodontal tissue regeneration [29]. DPSCs apoptosis decreased in hypoxic environment or serum-free medium while blood vessel regeneration increased when hepatocyte growth factor (HGF) gene was transfected. Notably, both the DPSCs and DPSC-HGF injection contributed to periodontal alveolar bone regeneration and soft tissue healing, but the alveolar bone volume and the percentage of bone tissue in the periodontium in the DPSC sheets group were higher [30]. Existing preclinical studies showed that DPSCs and DPSC-HGF sheets were able to significantly improve periodontal bone regeneration, but the underlying mechanisms and longer-term effects need to be further investigated.

Tooth loss is another common dental disease. Nowadays, biologically inactive dental implants have become the most commonly used method for teeth restoration [31]. There is no periodontal connection built between implants and alveolar bone, leading to disability of distributing chewing pressure and failed feeling changes in temperature or pressure because of a lack of pulp tissue. One regenerative strategy uses stem cells, graft materials, and cell-signalling molecules mimicking the interlayer structure of natural teeth, which contains periodontal tissue, dentin, and pulp, to regenerate the ideal root. Periodontal tissue-like fibres were found on the lateral side of TDM, a large amount of predentin like tissue was found on the pulp side of TDM 12 weeks after transplantation with DPSC sheets, treated with dentin matrix (TDM) and matrigel, and odontoblast like cells were found near and inside the regenerated predentin as well. TDM can release dentin sialophosphoprotein (DSPP), dentin matrix protein 1 (DMP-1), transforming growth factor-β (TGF-β) and other growth factors to create a favourable induced microenvironment for root regeneration. Upregulation of vascular endothelial growth factor receptor 1 (VEGFR1) and Nestin, CD31 and β3-tubulin in regenerative pulp-like tissue indicated that the composite structure with the DPSC sheets can promote pulp and bone regeneration [32]. In summary, there might be a new way of root regeneration in the future.

Recently, decellularized tissues have been applied to regenerative medicine, including human peripheral nerves, skeletal muscle and cardiac tissue. The regeneration function of decellularized pulp tissues has drawn wide attention. For example, a study demonstrated that DPSCs seeded onto decellularized dental pulp showed 3-dimensional attachment and proliferation, in which cell differentiation was observed near the dentinal wall. Increased expression of odontoblastic markers and cellular projections into dentinal tubules posed a positive influence on endodontic regeneration [33]. In another similar study, ECM harvested from decellularized pulp tissues was implanted into the root canals of beagle dogs for 8 weeks. At the end, CD31-positive and dentin sialoprotein (DSP)-positive tissues were found in the root canals, indicating the formation of neovascularization and dental pulp-like tissue, respectively. In addition, mineralized tissue was formed in the root canal, which was attributed to the differentiation of DPSCs into cementoblasts. It is widely believed that cementogenesis inhibitors are needed to prevent mineralization in the root canal during pulp regeneration. However, dental pulp tissue ECM has a positive and reliable effect on tissue reconstruction and site-appropriate tissue regeneration, which is likely attributed to dECM providing cells a niche environment, including unique pattern of distribution and functional components [34]. At the present, researches on DMSCs dECM were limited; however, it may become a new direction of stem cells therapy soon due to its excellent regenerative potential, multifunction and flexibility as a biomaterial, as well as making up for immune rejection and shortage of sources.

Bone regeneration of DPSC sheets

Bone defects can be caused by a variety of diseases, injuries, or congenital developmental abnormalities, which are usually treated by autologous or allogeneic bone grafts. However, limited donor bone, secondary surgical trauma, simultaneous immunosuppressive therapy, an elevated risk of infection from bacteria or viruses and postoperative instability can also lead to problems during the treatment. Hence, an effective yet safe regenerative treatment for bone defects is expected. Based on the osteogenic differentiation potential of DPSCs, researchers have attempted to apply DPSC sheets to bone fractures in order to promote bone tissue growth. 4-(4-Methoxyphenyl) pyrido [40,30:4,5] thieno [2,3-b] pyridine-2-carboxamide (TH) is a helioxanthin derivative. After the transplantation of the TH-treated DPSC sheets into the skull defect, bone regeneration was significantly promoted, and the DPSC sheets were covering defects throughout the entire repair period [22, 35]. It has been demonstrated that DPSC sheets have higher immunosuppressive activity and better ability to suppress T cell responses compared to BMSCs. Aging causes different changes in various tissues and organs, such as volume reduction in dental pulp tissue, resulting in the number of DPSCs collected from the lost teeth of elderly patients is less than that obtained from young patients. However, as for the process of promoting bone formation, no significant difference was found when comparing DPSCs from young and older individuals. What is interesting is that DPSCs from elderly individuals still show a strong bone regeneration ability because the telomere length remained stable from P1 to P3. It is possible that once DPSCs obtained ‘stemness’ after passing a specific stage, the proliferation and differentiation potential are independent from the aging process [36]. As a consequence, the age of the donor will not be a major limiting factor in future clinical applications. Three-dimensional cell culture refers to the co-culture of scaffolds and cells with different three-dimensional structures in vitro that could establish the physiological interaction between cells and the cell-extracellular matrix to simulate the specificity of natural tissue to the greatest extent [37]. Using three-dimensional cell culture technology, the single DPSC sheet was constructed into a spherical tissue-engineered structure, which promoted the differentiation of DPSCs into mature osteoblasts, displayed the related gene expression of osteoblasts, collagen type 1 (Col 1) was expressed widely from the surface layer of the tissue structure to its centre and induced the accumulation of a large amount of bone matrix protein and calcified matrix grafting to the bone defect site to promote bone regeneration. In the regeneration process, COL 1 acts as a scaffold on which a calcified matrix is deposited, eventually forming bone tissue [38].

Nervous system regeneration of DPSC sheets

Attributed to be of neural crest origin, DPSCs show remarkable neurogenic potential and have been applied to many neurodegenerative diseases and nerve injuries, including Alzheimer's disease, Parkinson’s disease and spinal cord injury. However, the number of transplanted DPSCs is much lower than anticipated [39]. Therefore, the DPSC sheets may be a better choice to reach ideal nerve generation. Facial nerve injury is a type of peripheral nerve injury. The proportion of axon regeneration is cogent evidence of nerve function repair. After transplanted DPSC sheets to facial nerve, they can stay in the injured site for a long time and produce a large amount of neurotrophic factor (NTF) protein, including brain-derived neurotrophic factor (BDNF), glial cell-derived neurotrophic factor (GDNF) and neurotrophic factor-3 (NT3), which have been demonstrated to have roles in peripheral nerve development and repair. DPSC sheets act as an NTF transmission system to promote axon extension and significantly enhance nerve regeneration. All these results suggest the optimistic outlook of DPSC sheets for the treatment of peripheral nerve injury [40]. Currently, new biomaterials, such as nerve conduits and porous scaffolds, are widely used in the treatment of peripheral nerve injury and spinal cord injury. Upon binding with bFGF, chitosan scaffolds activated the extracellular signal-regulated kinase (ERK) pathway and enhanced the expression of neural markers in DPSCs [41, 42]. Heparin-poloxamer (HP), a thermosensitive material that transforms into hydrogel structure at body temperature, improved the motor function recovery of a rat spinal cord injury model and reduced the release of pro-inflammatory factors around the injury sites after grafted in vivo combined with DPSCs [43, 44]. Nerve conduits, which are made from biodegradable materials, have become reliable clinical scaffold materials for peripheral nerve injury treatment. In combination of recombinant human basic fibroblast growth factor and DPSCs, cells differentiated into neurons and Schwann-like cells and formed myelinated nerve fibres, which confirmed that the conduit could promote nerve repair and regeneration in vivo [45]. The combination of these scaffold materials and cell sheets to provide bioactive components by ECM has been preliminarily explored, and it is believed that this is a treatment method that can be expected to achieve better nerve regeneration effects in future.

In addition, DPSC sheets are also applicable to other tissue regeneration treatments. In an animal model of total limbal stem cell deficiency (LSCD), DPSC sheets enabled better functional regeneration and transparency of damaged corneas in mice and expressed limbal stem cell markers in in vitro culture [46]. To summarize, DPSC sheets had been proved to be effective in the regeneration of dental tissue, bone tissue, nerve tissue and cornea. The regenerated tissue from DPSC sheets contained more angiogenesis and the fibrous structure was more porous, similar to loose connective tissue, indicating that they are more suitable for regeneration of dental pulp or vascular rich tissues. In addition, DPSC seems to show stronger stemness during the cell sheets formation. The expression of related genes to self-renewing and stemness maintenance of mesenchymal stem cells in DPSC sheets is also higher than that in other DMSC sheets [26], suggesting that DPSC sheets are likely to differentiate into multi-line tissues under certain conditions. Therefore, according to the characteristics of DPSC and the existing experimental results, DPSC can achieve the regeneration of a variety of tissues, but it is especially suitable for loose tissues containing blood vessels. Currently, clinical studies have not been performed, and the regeneration and potential side effects of DPSC sheets in human need to be further explored.

PDLSC sheets applications

PDLSCs are mesenchymal-derived stem cells isolated from the periodontal ligament. It has been previously confirmed that PDLSCs have the potential for cementum and osteogenic differentiation [3], which can form a three-dimensional periodontal ligament tissue-like structure [47], and have the potential to differentiate into endothelial cells, cardiomyocytes and retinal ganglia-like cells [48]. Because of the multilineage differentiation potential, PDLSC sheets have been used in periodontal tissue, bone tissue, and corneal regeneration. In the future, a wider application of PDLSC sheets treating diseases is expected.

Periodontal tissue regeneration of PDLSC sheets

Periodontal tissue incorporates cementum, periodontal ligament and alveolar bone. This complex structure characterized by bone and ligament connects soft and hard tissues functionally and endows natural teeth with physiological functions, such as reducing excessive occlusal force, carrying out corrective movement through bone remodelling and perceiving harmful stimulation. PDLSCs exhibit osteoblast-like characteristics and are able to differentiate into osteoblasts or osteoblasts. They are also considered as the optimal seed cells for periodontal regeneration [49].

A biphasic scaffold is formed by solution electrospinning and melt electrospinning, and then the cell sheets are combined to form the final multiphasic construct. An important feature of this construct is that it ensures sufficient biomechanical stability to maintain close contact between the cell sheet and the root surface, thereby facilitating attachment to the root surface. It was found that the multiphasic construct with PDLSC sheets could achieve satisfying periodontal tissue regeneration. Although regenerated periodontal tissue contained implanted PDLSCs, most of the cells involved in the formation of mature regenerated tissue were from surrounding host tissue [50]. However, the implantation of biphasic scaffolds with primary GMSC sheets inhibited the recovery of periodontal tissue. This might be because GMSCs primary culture consists of a heterogeneous population of terminally differentiated fibroblasts and progenitor cells, which are not beneficial to periodontal regeneration [51]. Titania nanotubular topography has been widely proven to be a powerful regulator of cell shape, adhesion, proliferation and differentiation. However, it has never been reported whether the function of PDLSCs can be modulated by nanotopography [52, 53]. The nanomorphology of the titanium surface, after surface treatment, can provide cues for periodontal regeneration and enhance the adhesion and diffusion of PDLSCs and the secretion of collagen in the initial stage after the implantation of sheets and significantly improved the PDLSCs differentiation into periodontal ligament (PDL) cells in the sheets, generation of PDL-like dense collagen fibres and vascular regeneration also occurred [54]. In addition to using the cell sheets in combination with other scaffolds, the use of PDLSC sheets to self-form a cylindrical structure also achieved excellent regeneration effects. After the cultured PDLSC sheets formed a cylindrical structure, the scaffold-free structure formed a PDL-like fibrous structure outside and mineralized tissue inside. In addition, the PDL-like structure in vitro was parallel to the cementum. When exposed to the mechanical stimulation microenvironment of the natural periodontal tissue, the arrangement of cells and ECM in the tissue changed to some extent, suggesting that moderate mechanical stimulation is important for the structure and morphology of the periodontal tissue [55]. A previous study suggested that individual PDLSCs transduced with recombinant human bone morphogenetic protein-2 (rhBMP-2) promoted the formation of mineralized tissue [56]. In another study, rhBMP-2 pretreatment promoted collagen fibre formation from PDLSC sheets and cementogenic differentiation. Cementum-like mineralized tissue with vertical or oblique insertion of collagen fibres onto the micro-/macro-porous biphasic calcium phosphate (MBCP) structure surface were formed [57]. Nano morphology, self-formed structure or additional inducers, these treatment factors facilitated the tissue regeneration from different perspectives and mechanisms. To explore the cell sheets with fewer side effects and better regeneration effects, pre-treated DMSC, combining with other biological scaffold materials, or additional treatment can be taken into consideration.

With the wide application of titanium implants in the restoration of missing teeth, increasing attention has been given to peri-implant inflammation. Without timely intervention, it will lead to rapid progression of inflammation, bone destruction, and ultimately failure of implant surgery [31]. One of the strategies of peri-implantitis regeneration therapy is cell sheet technology. PDL-like fibrous tissue was observed on the surface of the implant after the titanium rod wrapped with PDLSC sheets were implanted into the jaw defect. The calcium phosphate coating has been proven to accelerate the calcification of osteoblasts, and the coating can improve the attachment of PDL cells to the surface of titanium. An important function of the periodontal ligament is to buffer the occlusal load and maintain alveolar bone height. This important physiological function is missing due to the titanium implant and jawbone direct combination. Therefore, the ability to generate periodontal tissue around the implant with the cell sheets technique is of great significance to dental health [58]. Most experiments with cell sheets have been conducted at the cellular level and in animal models, but the regenerative effect of PDLSC sheets have been validated in patients with periodontitis. The availability of autologous suitable, redundant healthy periodontal tissue is often a limiting factor for periodontitis patients; however, owing to the immunomodulatory role of MSCs, suitable allogenic tissue may also be a reliable source [16]. Decellularized periodontal ligament ECM retains its original structure, effectively supports the regeneration of pericementum PDLSCs, and expresses cementum- and periodontal ligament-related genes after reseeding PDLSCs onto ECM [59]. In summary, the integration of autologous MSCs with a decellularized periodontal scaffold may be a promising approach to promote PDL regeneration.

Bone regeneration of PDLSC sheets

The potential for osteogenic differentiation of PDLSCs has been demonstrated by the formation of calcified nodules and the expression of alkaline phosphatase (ALP), matrix extracellular protein, bone sialoprotein (BSP), osteocalcin (OCN) and TGF-β receptor I [3]. Recently, a variety of treatments have been applied to improve the regeneration effect of PDLSC sheets, including the addition of active molecules during the culture of cell sheets, modification of scaffold structure and gene transfection. Previous studies have demonstrated that platelet-rich fibrin (PRF) can promote the regeneration of oral tissues. During the fabrication of PDLSC sheets, PRF treatment promoted the proliferation of PDLSCs and induced osteogenic differentiation by increasing the expression of the runt-related transcription factor 2 (RUNX2), BSP, osteopontin (OPN), and OCN genes [60]. Osthole is a small molecular compound extracted from traditional Chinese medicine that has been reported to promote the proliferation and differentiation of osteoblasts [61, 62]. After treatment with Osthole, the levels of osteogenic-related genes and proteins in PDLSC sheets were significantly improved, and more bone formation was observed in vivo [63]. Gold nanoparticles (AuNPs) are novel biocompatible materials, and AuNPs have been reported to promote the osteogenic differentiation of PDLSCs in a particle size-dependent manner [64, 65]. When AuNPs were added to PDLSC sheets, the CT, bone staining and bone formation-related protein results showed more new bone formation [66].

Indirectly co-cultured technology is another way to promote bone regenerative potential of PDLSC sheets. It has been suggested that co-culture with jawbone marrow-derived mesenchymal stem cells, endothelial cells, and osteoblastic progenitor cells can promote the proliferation and differentiation of PDLSCs [67,68,69]. Bladder epithelial stem cells have multilineage potential and can effectively alleviate severe hindlimb ischaemia through paracrine action [70]. Taking advantage of paracrine signalling, the osteogenic differentiation of PDLSC sheets in vitro and in vivo was improved by co-culture with bladder epithelial stem cells [71]. Type IV collagen A2 (COL4A2) is one of the major structural components of the basement membrane, it can bind to bone morphogenetic proteins involved in angiogenesis and osteogenesis (such as osteogenin and osteogenic protein-1). The binding protein is presented in an immobilized form to stem cells and osteoprogenitor-like cells to initiate osteogenesis. When PDLSCs were cultured on decellularized BMSCs ECM (B-dECM) and decellularized PDLSCs ECM (P-dECM), PDLSCs showed stronger proliferation, stemness and osteogenic differentiation abilities. Additionally, the upregulation of COL4A2 in P-dECM inhibited the Wnt pathway and promoted osteogenic differentiation of PDLSCs [72]. Bone regeneration is a more complicated process than osteogenesis and physical function recovery. With the constant development of the PDLSC sheets for promoting bone formation, genetic modification may become another promising method at the same time [73]. In short, how to better improve the function of the sheets is still a problem worthy of in-depth study.

Corneal regeneration of PDLSC sheets

DPSC sheets were shown to have the potential to promote corneal injury regeneration, analogously, PDLSC sheets showed regenerative effects on corneas. The cornea is a protruding structure in which cells are subjected to dome-shaped strain. In vitro, the dome-shaped mechanical stimulation can promote the multilayer, transparent structure of PDLSC sheets and the expression of corneal stroma markers with keratocyte inducing medium synergically. Tendon is very similar to the corneal stroma in structure, composition and gene expression profile, and significantly upregulation of tendon related genes was observed when BMSCs were treated with similar mechanical and chemical stimulation. In the future, more effective ways alone or in combination with chemical stimulation can be found by refining the mechanical stress to promote better corneal regeneration [74].

The current conventional method of sheets harvest requires approximately 10 days of culture, which is a barrier to clinical application. To address this problem, an appropriate method should be selected to store the obtained cell sheets while ensuring that its structural integrity and biological activity are not damaged. Cryopreservation has become a storage method for a variety of biological materials. By comparing the PDLSC sheets that had been cryopreservated for 3 months with the freshly prepared cell sheets, it was found that there was no significant difference in the cell proliferation rate, cell activity or karyotype analysis between the two types. The bone-like matrix formed in the body showed a network of type I and III collagen that were closely connected with each other, indicating that cryopreservation is a reliable treatment to preserve PDLSC sheets [75]. Nonetheless, whether longer treatment would cause damage to the biological activity and function of the cell sheets calls for further investigation.

Studies about regeneration of PDLSC sheets involving dental tissue, bone tissue and cornea will also have a positive impact on regeneration therapy of other tissues in the future. PDLSC sheets show better regeneration effects in periodontal tissue when compared to other tissues.

Other DMSC sheets applications

In addition to DPSC sheets and PDLSC sheets, which have been widely applied to various regenerative therapies, other dental stem cell sheets currently used in regenerative medicine include DFSC, ABMSC and SHED sheets (Fig. 3 and Table 1). These cell sheets have been applied to dental tissue regeneration, but the applications of other diseases or tissue defects need further exploration.

Fig. 3
figure 3

DMSC sheets in different tissues regeneration. DPSC sheets application dental tissue, bone, nervous system and cornea regeneration; PDLSC sheets application dental tissue, bone and cornea regeneration; SHED sheets application dental root regeneration; DFSC sheets application periodontal tissue regeneration; ABMSC sheets application bone regeneration. Bone; Nervous system; Cornea; Root; Dental pulp; periodontal tissue. The elements of bone, nervous system and cornea were obtained from the Smart Servier website:

Table 1 Regeneration of DMSC sheets in different study models

DFSCs express a higher level of colony-forming ability and osteogenic-related markers such as RUNX2, ALP and DSPP than DPSCs and PDLSCs [9]. Hertwig's epithelial root sheath (HERS) cells play an important role in the development of the root by secreting proteins related to tooth development, guiding DFSCs attachment to the newly formed root dentin [76] and acting as the signal centre for the development of the root [77]. Based on the above characteristics, sheets harvested from DFSCs co-cultured with HERS can form cementum and periodontal ligament-like tissue in vivo [78]. Although DFSCs and PDLSCs share similar mesenchymal origins, their respective cell sheets have different characteristics in the inflammatory microenvironment. In the experimental animal model of periodontitis, the bone regeneration in DFSC sheets group was more than PDLSCs group and was basically similar to normal bone tissue. Although the expression of osteogenic genes in PDLSC sheets were superior to that in DFSC sheets, the opposite result was shown in the inflammatory state. This may be the result of embryonic characteristics of DFSCs providing a favourable stem cell niche for periodontal regeneration [79]. In the process of periodontal regeneration, a certain space is needed. DFSC sheets were combined with decalcified dentin matrix (DDM) and hydroxyapatite/tricalcium phosphate to form a composite structure. It had a certain support strength and maintained a certain space during periodontal regeneration. Stem cells in DFSC sheets are conducive to long-term stable microvascular growth and blood supply, as well as to periodontal ligament, cementum and alveolar bone regeneration [80]. DFSC sheets combined with treated dentin matrix particles (TDMP) have similar regeneration effects [81].

BMSC sheets have been verified to be effective in bone regeneration in previous studies [82], but the application of BMSCs has many limitations, such as the invasive and painful process of collecting samples from the iliac crest, inflammatory stimulation and impairment in differentiation and stemness due to the age of the donor [83]. Compared with iliac-derived MSCs (Lon-BMSCs), the acquiring procedure of ABMSCs shows less trauma, more proliferation and osteogenesis abilities. ABMSC sheets had higher osteogenic differentiation and bone defect reconstruction ability than Lon-BMSCs sheets in the rabbit bone defect model after 4 weeks of treatment, implying, the degree of recovery of osteogenic-related genes and bone defect area was higher. Moreover, T helper 1 (Th1), type 1 macrophages (M1) and type 2 macrophages (M2) had no significant difference in different groups, indicating that the immunoregulation function of Lon-BMSCs and ABMSCs had no differentiation. ABMSCs exhibited immunosuppressive effects on monocyte activation and T cell activation and proliferation similar to Lon-BMSCs, both of them drove macrophages into an anti-inflammatory M2 phenotype [84].

SHED is another important type of DMSCs that is much younger than DPSCs and is predicted to possess the potential to regenerate periodontal tissues. To explore the potential of SHED in root regeneration, SHED sheets were grafted with TDM into the subcutaneous and jawbone of nude mice and rats. The osteogenic and odontogenic genes and proteins were upregulated after 14 days of induction, and dentin and periodontal tissue regeneration were also observed. Therefore, SHED sheets are promising materials that can be applied for biological root construction therapy and clinical applications. The remarkable protein synthesis and secretion functions of SHED can form a local microenvironment conducive to tissue repair and regeneration. L-Ascorbic acid, a component of cell sheets formation medium and osteogenic induction medium, is beneficial to the autocrine and paracrine functions of cells and promote the synthesis and accumulation of ECM, which may be a key factor in promoting a beneficial microenvironment [85]. SCAP sheets, from the DMSC sheets category, have the highest mineral tissue formation, being suitable for mineralized tissue formation [26]. Although the above cell sheets show multidirectional differentiation potential, DPSCs, PDLSCs and SCAPs showed no significant difference regarding tissue structure and ECM protein expression. They have unique features and work on various tissue regeneration differently. In the future, merits and demerits of different DMSC sheets can be further investigated, as well as their application.

Cell sheet technology has made remarkable progress since its first invention. Nevertheless, the applications of this technology are still in their infancy, and shortcomings should not be ignored. The following are problems during cell sheets culture. First of all, DMSC sheet culture generally takes about 14 days which is not suitable for urgent use. Secondly, the quality of cell sheets obtained from different batches of cell sources varies widely and the high cost of the culture process makes mass production hard. Besides, personalized and accurate repair is impossible with current technology, but the combination of cell sheets and 3D printing technology is likely to be a potential solution [37]. On the other hand, the transplantation and transport of single-cell sheet mechanical property is also worth noticing. Simple cell sheets transplantation usually does not generate blood vessels by themselves, and multilayer cell sheets applied to large or deep tissue defects may be difficult to ensure nutritional supply after transplantation with a possible affected cell viability. Moreover, the infection risks, trauma from transplantation, immune-related rejection, oncogenicity and other potential side effects should not be ignored. In order to minimize the damage and avoid postoperative infection, it is recommended to follow the transplant instructions strictly, use minimally invasive methods and perform aseptic practice all the time. Generally, autologous cells are characterized by an extremely low probability of triggering an immune response, but unfortunately autologous cells are very limited and are subjected to donors' physical condition [16, 86]. The usage of immunosuppressant or decellularization of allogeneic cell sheets may be required to reduce immune response if necessary. Limited research has shown that the high-density cellular interconnection structure of the cell sheets can directly promote the regeneration of target tissues, and the underlying mechanisms have not been clarified. The dynamics of cell migration from the cell sheets and its role in tissue formation in vivo, the integration of the cell sheets in vivo and the extent to which cells contribute directly to regeneration are needed to be unfold [87]. As for practical application, scientific supervision systems and standardized training for relevant practitioners is inevitable. Currently in Japan, relevant laws and regulations have been issued [88], which has set up a great example for other countries and regions.


Current studies have confirmed that a variety of DMSC sheets could promote the regeneration of abundant tissues, showing vigorous regeneration and repair potential in dental tissue, bone, nerve and corneal regeneration. Although the regenerative effect of DMSC sheets is encouraging, not all DMSC sheets can promote tissue regeneration in vivo, the way of choosing the suitable seed cells correctly is essential. Additionally, the DMSC sheets themselves also need more reform. Some improvements, such as combining them with drugs or bioactive molecules, or integrated with scaffold, are necessary. The reformed DMSC sheets are expected to manage cell metabolism or biological reactions in the body. Currently, the technology and application of cell sheets are basically limited to the vitro histology and animal models and few clinical trials, more complicated clinical situations need to be considered to transform them into widespread clinical applications. Moreover, the mass production and long-term effective preservation method and trauma remain unresolved. Moreover, existing researches have not deeply discussed the mechanism and the role between specific components in cell sheets and tissue regeneration needs to further explode.

Availability of data and materials

Not applicable.



Alveolar bone-derived mesenchymal stem cells


Adipose-derived stem cells


Alkaline phosphatase


Gold nanoparticles


Decellularized bone marrow mesenchymal stem cell ECM


Brain-derived neurotrophic factor


Bone marrow mesenchymal stem cells


Bone sialoprotein

COL 1:

Collagen type 1


Type IV collagen A2


Composite membrane


Decellularized extracellular matrix


Decalcified dentin matrix


Dental follicle stem cells


Dentin matrix protein 1


Dental-derived mesenchymal stem cells


Dental pulp stem cells


Dentin sialophosphoprotein


Extracellular matrix


Extracellular signal-regulated kinase


Glial cell-derived neurotrophic factor


Gingival mesenchymal stem cells


Hertwig’s epithelial root sheath


Hepatocyte growth factor




Light-emitting diode


Iliac-derived MSC


Limbal stem cell deficiency


Micro-/macro-porous biphasic calcium phosphate


Type 1 macrophages


Type 2 macrophages


Mesenchymal stem cells


Neurotrophic factor-3


Neurotrophic factor






Photobiomodulation therapy


Decellularized PDLSC


Periodontal ligament


Periodontal ligament stem cells


Platelet-rich fibrin


Recombinant human bone morphogenetic protein-2


Reactive oxygen species


Runt-related transcription factor 2


Stem cells from the apical papilla


Stem cells from human exfoliated deciduous teeth


Tributyl phosphate


Treated dentin matrix


Treated dentin matrix particles


Transforming growth factor β


Tooth germ stem cells




T helper 1


Temperature-responsive polymer-grafted cell culture dishes


Umbilical cord mesenchymal stem cell


Vascular endothelial growth factor receptor 1


  1. Gronthos S, Mankani M, Brahim J, Robey PG, Shi S. Postnatal human dental pulp stem cells (DPSCs) in vitro and in vivo. Proc Natl Acad Sci U S A. 2000;97(25):13625–30.

    CAS  PubMed  PubMed Central  Google Scholar 

  2. Miura M, Gronthos S, Zhao M, et al. SHED: stem cells from human exfoliated deciduous teeth. Proc Natl Acad Sci U S A. 2003;100(10):5807–12.

    CAS  PubMed  PubMed Central  Google Scholar 

  3. Seo BM, Miura M, Gronthos S, Mark Bartold P, Batouli S, Brahim J, et al. Investigation of multipotent postnatal stem cells from human periodontal ligament. Lancet. 2004;364(9429):149–55.

    CAS  PubMed  Google Scholar 

  4. Sonoyama W, Liu Y, Yamaza T, et al. Characterization of the apical papilla and its residing stem cells from human immature permanent teeth: a pilot study. J Endod. 2008;34(2):166–71.

    PubMed  PubMed Central  Google Scholar 

  5. Zhang Q, Shi S, Liu Y, Uyanne J, Shi Y, Shi S, et al. Mesenchymal stem cells derived from human gingiva are capable of immunomodulatory functions and ameliorate inflammation-related tissue destruction in experimental colitis. J Immunol. 2009;183(12):7787–98.

    CAS  PubMed  Google Scholar 

  6. Morsczeck C, Moehl C, Götz W, et al. In vitro differentiation of human dental follicle cells with dexamethasone and insulin. Cell Biol Int. 2005;29(7):567–75.

    CAS  PubMed  Google Scholar 

  7. Ikeda E, Yagi K, Kojima M, Yagyuu T, Ohshima A, Sobajima S, et al. Multipotent cells from the human third molar: feasibility of cell-based therapy for liver disease. Differentiation. 2008;76(5):495–505.

    CAS  PubMed  Google Scholar 

  8. Matsubara T, Suardita K, Ishii M, Sugiyama M, Igarashi A, Oda R, et al. Alveolar bone marrow as a cell source for regenerative medicine: differences between alveolar and iliac bone marrow stromal cells. J Bone Miner Res. 2005;20(3):399–409.

    CAS  PubMed  Google Scholar 

  9. Gan L, Liu Y, Cui D, Pan Y, Zheng L, Wan M. Dental tissue-derived human mesenchymal stem cells and their potential in therapeutic application. Stem Cells Int. 2020;2020:8864572.

    PubMed  PubMed Central  Google Scholar 

  10. Liu J, Yu F, Sun Y, Jiang B, Zhang W, Yang J, et al. Concise reviews: characteristics and potential applications of human dental tissue-derived mesenchymal stem cells. Stem Cells. 2015;33(3):627–38.

    CAS  PubMed  Google Scholar 

  11. Fang F, Zhang K, Chen Z, Wu B. Noncoding RNAs: new insights into the odontogenic differentiation of dental tissue-derived mesenchymal stem cells. Stem Cell Res Ther. 2019;10(1):297.

    PubMed  PubMed Central  Google Scholar 

  12. Yamada Y, Nakamura-Yamada S, Kusano K, Baba S. Clinical potential and current progress of dental pulp stem cells for various systemic diseases in regenerative medicine: a concise review. Int J Mol Sci. 2019;20(5):1132.

    CAS  PubMed Central  Google Scholar 

  13. Okano T, Yamada N, Sakai H, et al. A novel recovery system for cultured cells using plasma-treated polystyrene dishes grafted with poly (N-isopropylacrylamide). J Biomed Mater Res. 1993;27(10):1243–51.

    CAS  PubMed  Google Scholar 

  14. Kim BS, Das S, Jang J, Cho D. Decellularized extracellular matrix-based bioinks for engineering tissue- and organ-specific microenvironments. Chem Rev. 2020;120(19):10608–61.

    CAS  PubMed  Google Scholar 

  15. Alblawi A, Ranjani AS, Yasmin H, Gupta S, Bit A, Rahimi-Gorji M. Scaffold-free: a developing technique in field of tissue engineering. Comput Methods Prog Biomed. 2020;185:105148.

    Google Scholar 

  16. Iwata T, Yamato M, Washio K, Yoshida T, Tsumanuma Y, Yamada A, et al. Periodontal regeneration with autologous periodontal ligament-derived cell sheets—a safety and efficacy study in ten patients. Regen Ther. 2018;9:38–44.

    PubMed  PubMed Central  Google Scholar 

  17. Kashiyama N, Kormos RL, Matsumura Y, et al. Adipose-derived stem cell sheet under an elastic patch improves cardiac function in rats after myocardial infarction. J Thorac Cardiovasc Surg. 2020;S0022–5223(20):31139–49.

    Google Scholar 

  18. Khalili M, Asadi M, Kahroba H, Soleyman MR, Andre H, Alizadeh E. Corneal endothelium tissue engineering: an evolution of signaling molecules, cells, and scaffolds toward 3D bioprinting and cell sheets. J Cell Physiol. 2021.

    Article  Google Scholar 

  19. Asadi M, Khalili M, Lotfi H, Vaghefi Moghaddam S, Zarghami N, André H, et al. Liver bioengineering: recent trends/advances in decellularization and cell sheet technologies towards translation into the clinic. Life Sci. 2021;276:119373.

    CAS  PubMed  Google Scholar 

  20. Imashiro C, Shimizu T. Fundamental technologies and recent advances of cell-sheet-based tissue engineering. Int J Mol Sci. 2021;22(1):425.

    CAS  PubMed Central  Google Scholar 

  21. Garrido PR, Pedroni ACF, Cury DP, Moreira MS, Rosin F, Sarra G, et al. Effects of photobiomodulation therapy on the extracellular matrix of human dental pulp cell sheets. J Photochem Photobiol B. 2019;194:149–57.

    CAS  PubMed  Google Scholar 

  22. Yamakawa D, Kawase-Koga Y, Fujii Y, Kanno Y, Sato M, Ohba S, et al. Effects of helioxanthin derivative-treated human dental pulp stem cells on fracture healing. Int J Mol Sci. 2020;21(23):9158.

    CAS  PubMed Central  Google Scholar 

  23. Chang D, Fan T, Gao S, Jin Y, Zhang M, Ono M. Application of mesenchymal stem cell sheet to treatment of ischemic heart disease. Stem Cell Res Ther. 2021;12(1):384.

    PubMed  PubMed Central  Google Scholar 

  24. Crapo PM, Gilbert TW, Badylak SF. An overview of tissue and whole organ decellularization processes. Biomaterials. 2011;32(12):3233–43.

    CAS  PubMed  PubMed Central  Google Scholar 

  25. Choudhury D, Yee M, Sheng ZLJ, Amirul A, Naing MW. Decellularization systems and devices: state-of-the-art. Acta Biomater. 2020;115:51–9.

    CAS  PubMed  Google Scholar 

  26. Hu L, Zhao B, Gao Z, Xu J, Fan Z, Zhang C, et al. Regeneration characteristics of different dental derived stem cell sheets. J Oral Rehabil. 2020;47(Suppl 1):66–72.

    CAS  PubMed  Google Scholar 

  27. Itoh Y, Sasaki JI, Hashimoto M, Katata C, Hayashi M, Imazato S. Pulp regeneration by 3-dimensional dental pulp stem cell constructs. J Dent Res. 2018;97(10):1137–43.

    CAS  PubMed  Google Scholar 

  28. Wang Z, Chen Z, Fang F, Qiu W. The role of adiponectin in periodontitis: current state and future prospects. Biomed Pharmacother. 2021;137:111358.

    CAS  PubMed  Google Scholar 

  29. Hu J, Cao Y, Xie Y, et al. Periodontal regeneration in swine after cell injection and cell sheet transplantation of human dental pulp stem cells following good manufacturing practice. Stem Cell Res Ther. 2016;7(1):130.

    PubMed  PubMed Central  Google Scholar 

  30. Cao Y, Liu Z, Xie Y, et al. Adenovirus-mediated transfer of hepatocyte growth factor gene to human dental pulp stem cells under good manufacturing practice improves their potential for periodontal regeneration in swine. Stem Cell Res Ther. 2015;6:249.

    PubMed  PubMed Central  Google Scholar 

  31. Chen Z, Wang Z, Qiu W, Fang F. Overview of antibacterial strategies of dental implant materials for the prevention of peri-implantitis. Bioconjugate Chem. 2021;32(4):627–38.

    CAS  Google Scholar 

  32. Meng H, Hu L, Zhou Y, Ge Z, Wang H, Wu C, et al. A sandwich structure of human dental pulp stem cell sheet, treated dentin matrix, and matrigel for tooth root regeneration. Stem Cells Dev. 2020;29(8):521–32.

    CAS  PubMed  Google Scholar 

  33. Alghutaimel H, Yang X, Drummond B, Nazzal H, Duggal M, Raïf E. Investigating the vascularization capacity of a decellularized dental pulp matrix seeded with human dental pulp stem cells: in vitro and preliminaryin vivo evaluations. Int Endod J. 2021;54(8):1300–16.

    CAS  PubMed  Google Scholar 

  34. Alqahtani Q, Zaky SH, Patil A, Beniash E, Ray H, Sfeir C. Decellularized swine dental pulp tissue for regenerative root canal therapy. J Dent Res. 2018;97(13):1460–7.

    CAS  PubMed  Google Scholar 

  35. Fujii Y, Kawase-Koga Y, Hojo H, et al. Bone regeneration by human dental pulp stem cells using a helioxanthin derivative and cell-sheet technology. Stem Cell Res Ther. 2018;9(1):24.

    CAS  PubMed  PubMed Central  Google Scholar 

  36. Sato M, Kawase-Koga Y, Yamakawa D, Fujii Y, Chikazu D. Bone regeneration potential of human dental pulp stem cells derived from elderly patients and osteo-induced by a helioxanthin derivative. Int J Mol Sci. 2020;21(20):7731.

    CAS  PubMed Central  Google Scholar 

  37. Marconi GD, Porcheri C, Trubiani O, Mitsiadis TA. Three-dimensional culture systems for dissecting notch signalling in health and disease. Int J Mol Sci. 2021;22:12473.

    PubMed  PubMed Central  Google Scholar 

  38. Tatsuhiro F, Seiko T, Yusuke T, Reiko T, Kazuhito S. Dental pulp stem cell-derived, scaffold-free constructs for bone regeneration. Int J Mol Sci. 2018;19(7):1846.

    PubMed Central  Google Scholar 

  39. Luo Y, Qiu W, Wu B, Fang F. An overview of mesenchymal stem cell-based therapy mediated by noncoding RNAs in the treatment of neurodegenerative diseases. Stem Cell Rev Rep. 2021.

    Article  PubMed  Google Scholar 

  40. Ahmed MN, Shi D, Dailey MT, Rothermund K, Drewry MD, Calabrese TC, et al. Dental pulp cell sheets enhance facial nerve regeneration via local neurotrophic factor delivery. Tissue Eng Part A. 2021;27(17–18):1128–39.

    CAS  PubMed  Google Scholar 

  41. Zheng K, Feng G, Zhang J, Xing J, Huang D, Lian M, et al. Basic fibroblast growth factor promotes human dental pulp stem cells cultured in 3D porous chitosan scaffolds to neural differentiation. Int J Neurosci. 2021;131(7):625–33.

    PubMed  Google Scholar 

  42. Zhang J, Lu X, Feng G, Gu Z, Sun Y, Bao G, et al. Chitosan scaffolds induce human dental pulp stem cells to neural differentiation: potential roles for spinal cord injury therapy. Cell Tissue Res. 2016;366(1):129–42.

    CAS  PubMed  Google Scholar 

  43. Luo L, Albashari AA, Wang X, Jin L, Zhang Y, Zheng L, et al. Effects of transplanted heparin-poloxamer hydrogel combining dental pulp stem cells and bFGF on spinal cord injury repair. Stem Cells Int. 2018;2018:2398521.

    PubMed  PubMed Central  Google Scholar 

  44. Albashari A, He Y, Zhang Y, Ali J, Lin F, Zheng Z, et al. Thermosensitive bFGF-modified hydrogel with dental pulp stem cells on neuroinflammation of spinal cord injury. ACS Omega. 2020;5(26):16064–75.

    CAS  PubMed  PubMed Central  Google Scholar 

  45. Luo L, He Y, Jin L, Zhang Y, Guastaldi FP, Albashari AA, et al. Application of bioactive hydrogels combined with dental pulp stem cells for the repair of large gap peripheral nerve injuries. Bioactive Mater. 2021;6(3):638–54.

    CAS  Google Scholar 

  46. Gomes JA, Geraldes Monteiro B, Melo GB, Smith RL, Cavenaghi Pereira Da Silva M, Lizier NF, et al. Corneal reconstruction with tissue-engineered cell sheets composed of human immature dental pulp stem cells. Investig Ophthalmol Vis Sci. 2010;51(3):1408–14.

    Google Scholar 

  47. Iwata T, Yamato M, Zhang Z, Mukobata S, Washio K, Ando T, et al. Validation of human periodontal ligament-derived cells as a reliable source for cytotherapeutic use. J Clin Periodontol. 2010;37(12):1088–99.

    CAS  PubMed  Google Scholar 

  48. Trubiani O, Pizzicannella J, Caputi S, Marchisio M, Mazzon E, Paganelli R, et al. Periodontal ligament stem cells: current knowledge and future perspectives. Stem Cells Dev. 2019;28(15):995–1003.

    PubMed  Google Scholar 

  49. Li J, Wang Z, Huang X, et al. Dynamic proteomic profiling of human periodontal ligament stem cells during osteogenic differentiation. Stem Cell Res Ther. 2021;12(1):98.

    CAS  PubMed  PubMed Central  Google Scholar 

  50. Vaquette C, Saifzadeh S, Farag A, Hutmacher DW, Ivanovski S. Periodontal tissue engineering with a multiphasic construct and cell sheets. J Dent Res. 2019;98(6):673–81.

    CAS  PubMed  Google Scholar 

  51. Fawzy El-Sayed KM, Mekhemar MK, Beck-Broichsitter BE, Bähr T, Hegab M, Receveur J, et al. Periodontal regeneration employing gingival margin-derived stem/progenitor cells in conjunction with IL-1ra-hydrogel synthetic extracellular matrix. J Clin Periodontol. 2015;42(5):448–57.

    CAS  PubMed  Google Scholar 

  52. Zhao L, Liu L, Wu Z, Zhang Y, Chu PK. Effects of micropitted/nanotubular titania topographies on bone mesenchymal stem cell osteogenic differentiation. Biomaterials. 2012;33(9):2629–41.

    CAS  PubMed  Google Scholar 

  53. Zhao L, Mei S, Wang W, Chu PK, Zhang Y, Wu Z. Suppressed primary osteoblast functions on nanoporous titania surface. J Biomed Mater Res A. 2011;96(1):100–7.

    PubMed  Google Scholar 

  54. Gao H, Li B, Zhao L, Jin Y. Influence of nanotopography on periodontal ligament stem cell functions and cell sheet based periodontal regeneration. Int J Nanomed. 2015;10:4009–27.

    CAS  Google Scholar 

  55. Basu A, Rothermund K, Ahmed MN, Syed-Picard FN. Self-assembly of an organized cementum-periodontal ligament-like complex using scaffold-free tissue engineering. Front Physiol. 2019;10:422.

    PubMed  PubMed Central  Google Scholar 

  56. Jung IH, Lee SH, Jun CM, Oh N, Yun JH. Characterization of the enhanced bone regenerative capacity of human periodontal ligament stem cells engineered to express the gene encoding bone morphogenetic protein 2. Tissue Eng Part A. 2014;20(15–16):2189–99.

    CAS  PubMed  PubMed Central  Google Scholar 

  57. Park JY, Park CH, Yi T, Kim SN, Iwata T, Yun JH. rhBMP-2 pre-treated human periodontal ligament stem cell sheets regenerate a mineralized layer mimicking dental cementum. Int J Mol Sci. 2020;21(11):3767.

    CAS  PubMed Central  Google Scholar 

  58. Washio K, Tsutsumi Y, Tsumanuma Y, Yano K, Srithanyarat SS, Takagi R, et al. In vivo periodontium formation around titanium implants using periodontal ligament cell sheet. Tissue Eng Part A. 2018;24(15–16):1273–82.

    CAS  PubMed  Google Scholar 

  59. Son H, Jeon M, Choi H, Lee H, Kim I, Kang C, et al. Decellularized human periodontal ligament for periodontium regeneration. PLoS ONE. 2019;14(8):e0221236.

    CAS  PubMed  PubMed Central  Google Scholar 

  60. Wang ZS, Feng ZH, Wu GF, Bai SZ, Dong Y, Chen FM, et al. The use of platelet-rich fibrin combined with periodontal ligament and jaw bone mesenchymal stem cell sheets for periodontal tissue engineering. Sci Rep. 2016;6:28126.

    CAS  PubMed  PubMed Central  Google Scholar 

  61. Kuo P, Hsu Y, Chang C, Chang J. Osthole-mediated cell differentiation through bone morphogenetic protein-2/p38 and extracellular signal-regulated kinase 1/2 pathway in human osteoblast cells. J Pharmacol Exp Ther. 2005;314(3):1290–9.

    CAS  PubMed  Google Scholar 

  62. Ming L, Zhou J, Cheng G, Ma H, Chen K. Osthol, a coumarin isolated from common cnidium fruit, enhances the differentiation and maturation of osteoblasts in vitro. Pharmacology. 2011;88(1–2):33–43.

    CAS  PubMed  Google Scholar 

  63. Gao LN, An Y, Lei M, Li B, Yang H, Lu H, et al. The effect of the coumarin-like derivative osthole on the osteogenic properties of human periodontal ligament and jaw bone marrow mesenchymal stem cell sheets. Biomaterials. 2013;34(38):9937–51.

    CAS  PubMed  Google Scholar 

  64. Vial S, Reis RL, Oliveira JM. Recent advances using gold nanoparticles as a promising multimodal tool for tissue engineering and regenerative medicine. Curr Opin Solid State Mater Sci. 2017;21(2):92–112.

    CAS  Google Scholar 

  65. Zhang Y, Kong N, Zhang Y, Yang W, Yan F. Size-dependent effects of gold nanoparticles on osteogenic differentiation of human periodontal ligament progenitor cells. Theranostics. 2017;7(5):1214–24.

    CAS  PubMed  PubMed Central  Google Scholar 

  66. Zhang Y, Wang P, Wang Y, Li J, Qiao D, Chen R, et al. Gold nanoparticles promote the bone regeneration of periodontal ligament stem cell sheets through activation of autophagy. Int J Nanomed. 2021;16:61–73.

    Google Scholar 

  67. Wu Y, Cao H, Yang Y, Zhou Y, Gu Y, Zhao X, et al. Effects of vascular endothelial cells on osteogenic differentiation of noncontact co-cultured periodontal ligament stem cells under hypoxia. J Periodontal Res. 2013;48(1):52–65.

    CAS  PubMed  Google Scholar 

  68. Yu M, Wang L, Ba P, Li L, Sun L, Duan X, et al. Osteoblast progenitors enhance osteogenic differentiation of periodontal ligament stem cells. J Periodontol. 2017;88(10):e159–68.

    CAS  PubMed  Google Scholar 

  69. Zhang H, Liu S, Zhu B, Xu Q, Ding Y, Jin Y. Composite cell sheet for periodontal regeneration: crosstalk between different types of MSCs in cell sheet facilitates complex periodontal-like tissue regeneration. Stem Cell Res Ther. 2016;7(1):168.

    PubMed  PubMed Central  Google Scholar 

  70. Zhu Q, Li Q, Niu X, Zhang G, Ling X, Zhang J, et al. Extracellular vesicles secreted by human urine-derived stem cells promote ischemia repair in a mouse model of hind-limb ischemia. Cell Physiol Biochem. 2018;47(3):1181–92.

    CAS  PubMed  Google Scholar 

  71. Yang X, Xiong X, Zhou W, Feng G, Zhang Y, Dai H, et al. Effects of human urine-derived stem cells on the cementogenic differentiation of indirectly-cocultured periodontal ligament stem cells. Am J Transl Res. 2020;12(2):361–78.

    CAS  PubMed  PubMed Central  Google Scholar 

  72. Wen Y, Yang H, Wu J, Wang A, Chen X, Hu S, et al. COL4A2 in the tissue-specific extracellular matrix plays important role on osteogenic differentiation of periodontal ligament stem cells. Theranostics. 2019;9(15):4265–86.

    CAS  PubMed  PubMed Central  Google Scholar 

  73. Jiang Z, Li N, Zhu D, et al. Genetically modified cell sheets in regenerative medicine and tissue engineering. Biomaterials. 2021;275:120908.

    CAS  PubMed  Google Scholar 

  74. Chen J, Zhang W, Backman LJ, Kelk P, Danielson P. Mechanical stress potentiates the differentiation of periodontal ligament stem cells into keratocytes. Br J Ophthalmol. 2018;102(4):562–9.

    PubMed  Google Scholar 

  75. Li M, Feng C, Gu X, He Q, Wei F. Effect of cryopreservation on proliferation and differentiation of periodontal ligament stem cell sheets. Stem Cell Res Ther. 2017;8(1):77.

    PubMed  PubMed Central  Google Scholar 

  76. MacNeil RL, Thomas HF. Development of the murine periodontium. II. Role of the epithelial root sheath in formation of the periodontal attachment. J Periodontol. 1993;64(4):285.

    CAS  PubMed  Google Scholar 

  77. Yamamoto H, Cho SW, Kim EJ, Kim JY, Fujiwara N, Jung HS. Developmental properties of the Hertwig’s epithelial root sheath in mice. J Dent Res. 2004;83(9):688–92.

    CAS  PubMed  Google Scholar 

  78. Bai Y, Bai Y, Matsuzaka K, Hashimoto S, Fukuyama T, Wu L, et al. Cementum- and periodontal ligament-like tissue formation by dental follicle cell sheets co-cultured with Hertwig’s epithelial root sheath cells. Bone. 2011;48(6):1417–26.

    CAS  PubMed  Google Scholar 

  79. Guo S, Kang J, Ji B, Guo W, Ding Y, Wu Y, et al. Periodontal-derived mesenchymal cell sheets promote periodontal regeneration in inflammatory microenvironment. Tissue Eng Part A. 2017;23(13–14):585–96.

    CAS  PubMed  Google Scholar 

  80. Feng G, Wu Y, Yu Y, Huang L, An S, Hu B, et al. Periodontal ligament-like tissue regeneration with drilled porous decalcified dentin matrix sheet composite. Oral Dis. 2018;24(3):429–41.

    CAS  PubMed  Google Scholar 

  81. Yang H, Li J, Hu Y, Sun J, Guo W, Li H, et al. Treated dentin matrix particles combined with dental follicle cell sheet stimulate periodontal regeneration. Dent Mater. 2019;35(9):1238–53.

    PubMed  Google Scholar 

  82. Kawecki F, Clafshenkel WP, Fortin M, Auger FA, Fradette J. Biomimetic tissue-engineered bone substitutes for maxillofacial and craniofacial repair: the potential of cell sheet technologies. Adv Healthc Mater. 2018;7(6):e1700919.

    PubMed  Google Scholar 

  83. Ma L, Hu J, Cao Y, Xie Y, Wang H, Fan Z, et al. Maintained properties of aged dental pulp stem cells for superior periodontal tissue regeneration. Aging Dis. 2019;10(4):793–806.

    PubMed  PubMed Central  Google Scholar 

  84. Liu Y, Wang H, Dou H, Tian B, Li L, Jin L, et al. Bone regeneration capacities of alveolar bone mesenchymal stem cells sheet in rabbit calvarial bone defect. J Tissue Eng. 2020.

    Article  PubMed  PubMed Central  Google Scholar 

  85. Yang X, Ma Y, Guo W, Yang B, Tian W. Stem cells from human exfoliated deciduous teeth as an alternative cell source in bio-root regeneration. Theranostics. 2019;9:2694–711.

    CAS  PubMed  PubMed Central  Google Scholar 

  86. Matsuura K, Utoh R, Nagase K, Okano T. Cell sheet approach for tissue engineering and regenerative medicine. J Control Release. 2014;190:228–39.

    CAS  PubMed  Google Scholar 

  87. Zurina IM, Presniakova VS, Butnaru DV, Svistunov AA, Timashev PS, Rochev YA. Tissue engineering using a combined cell sheet technology and scaffolding approach. Acta Biomater. 2020;113:63–83.

    CAS  PubMed  Google Scholar 

  88. Egami M, Haraguchi Y, Shimizu T, Yamato M, Okano T. Latest status of the clinical and industrial applications of cell sheet engineering and regenerative medicine. Arch Pharm Res. 2014;37:96–106.

    CAS  PubMed  Google Scholar 

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We thank the Smart Servier website: for providing freely medical art image materials.


This research was supported by grants from National Natural Science Foundation of China (82101024) and Natural Science Foundation of Guangdong Province (2020A1515011455, 2020A1515110027).

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WQ and FF contributed to the conception and design of the review. YC and WQ contributed to the writing and drafting of the manuscript, drew the figure and designed the table. HH, GL, JY, WQ and FF contributed to the critical revision of the manuscript for important intellectual content. All the authors have approved the final version of the manuscript to be published and agree to be accountable for all aspects of the work. All authors read and approved the final manuscript.

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Correspondence to Fuchun Fang or Wei Qiu.

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Chen, Y., Huang, H., Li, G. et al. Dental-derived mesenchymal stem cell sheets: a prospective tissue engineering for regenerative medicine. Stem Cell Res Ther 13, 38 (2022).

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  • Dental-derived mesenchymal stem cells
  • Cell sheets
  • Decellularized
  • Regenerative medicine