Effects of enamel matrix derivative on the proliferation and osteogenic differentiation of human gingival mesenchymal stem cells
- Shu-Man Wu†1, 2,
- Hsien-Chung Chiu†1,
- Yu-Tang Chin1, 3,
- Heng-Yi Lin1, 4,
- Cheng-Yang Chiang1,
- Hsiao-Pei Tu1, 5,
- Martin MJ Fu6 and
- Earl Fu7Email author
© Wu et al.; licensee BioMed Central Ltd. 2014
Received: 2 April 2013
Accepted: 28 January 2014
Published: 16 April 2014
Gingiva-derived mesenchymal stem cells (GMSCs) have recently been harvested and applied for rebuilding lost periodontal tissue. Enamel matrix derivative (EMD) has been used for periodontal regeneration and the formation of new cementum with inserting collagen fibers; however, alveolar bone formation is minimal. Recently, EMD has been shown to enhance the proliferation and mineralization of human bone marrow mesenchymal stem cells. Because the gingival flap is the major component to cover the surgical wound, the effects of EMD on the proliferation and mineralization of GMSCs were evaluated in the present study.
After single cell suspension, the GMSCs were isolated from the connective tissues of human gingiva. The colony forming unit assay of the isolated GMSCs was measured. The expression of stem cell markers was examined by flow cytometry. The cellular telomerase activity was identified by polymerase chain reaction (PCR). The osteogenic, adipogenic and neural differentiations of the GMSCs were further examined. The cell proliferation was determined by MTS assay, while the expression of mRNA and protein for mineralization (including core binding factor alpha, cbfα-1; alkaline phosphatase, ALP; and osteocalcin, OC; ameloblastin, AMBN) were analyzed by real time-PCR, enzyme activity and confocal laser scanning microscopy.
The cell colonies could be easily identified and the colony forming rates and the telomerase activities increased after passaging. The GMSCs expressed high levels of surface markers for CD73, CD90, and CD105, but showed low expression of STRO-1. Osteogenic, adipogenic and neural differentiations were successfully induced. The proliferation of GMSCs was increased after EMD treatment. ALP mRNA was significantly augmented by treating with EMD for 3 hours, whereas AMBN mRNA was significantly increased at 6 hours after EMD treatment. The gene expression of OC was enhanced at the dose of 100 μg/ml EMD at day 3. Increased protein expression for cbfα-1 at day 3, for ALP at day 5 and 7, and for OC at week 4 after the EMD treatments were observed.
Human GMSCs could be successfully isolated and identified. EMD treatments not only induced the proliferation of GMSCs but also enhanced their osteogenic differentiation after induction.
Mesenchymal stem cells (MSCs) are multipotent progenitor cells derived originally from adult bone marrow or some adult/fetal non-marrow tissues. Over recent years, several different MSCs have been harvested and identified from various dental tissues, including dental pulp stem cells [1, 2], stem cells from exfoliated primary teeth , periodontal ligament stem cells , dental follicle precursor cells from wisdom teeth , stem cells from periapical follicle  and gingiva-derived mesenchymal stem cells (GMSCs) . Because of their capabilities of multipotent differentiations, dental stem cells have been suggested as a potential candidate for tissue engineering and/or regenerative medicine. They can be used not only for regenerating dental tissues, but also for repairing non-dental tissues, such as bone and nerves [8, 9].
Periodontal disease is a common bacteria-associated inflammatory disease. The infective and inflammatory reactions from periodontal disease may damage the surrounding hard and soft tissue structures, called the periodontal attachment which requires alveolar bone, periodontal ligament and cementum, and results in tooth loss in the end [10, 11]. Numerous materials have been utilized to improve the regenerative treatment outcome of periodontal disease, including enamel matrix derivative EMD (Emdogain®, Institut Straumann AG, Basel, Switzerland). EMD (Emdogain®) is a purified acidic extract from the enamel matrix protein of the tooth bud and predominantly consists of amelogenins . The application of EMD in periodontal regenerative treatment has been widely focused on its ability to promote the formation of the lost periodontal attachment, especially on the regeneration of the periodontal ligament and cementum [13, 14]. Some studies have reported that EMD can also stimulate cellular proliferation and mineralization of pre-osteoblasts and osteoblasts [15–18]. On the other hand, some studies have reported that EMD reduces the differentiation of osteoblasts [19, 20]. Although a significant amount of new cementum has been widely observed following EMD application during periodontal treatments, the alveolar bone formation is reported to be minimal [21, 22].
To rebuild the lost periodontal attachment is the ultimate goal of periodontal therapy; however, true regeneration after the therapy is still challenging . Recently, dental stem cells have been reported as candidates to restore the lost periodontal tissue . In addition, it has recently been reported that EMD enhances the proliferation and mineralization of human bone marrow MSCs . Clinically, the EMD is applied to the tooth surfaces during periodontal regenerative surgery and covered with a gingival flap which is the main source of GMSCs. The effects of EMD on stem cells, especially on those derived from the local gingiva, have never been evaluated. The aim of the present study was to investigate the effects of EMD on the proliferation and mineralization of GMSCs.
Human gingiva-derived mesenchymal stem cells (hGMSCs)
Gingival tissue specimens were obtained from patients treated in the Periodontal Department of Tri-Service General Hospital from July 2009 to December 2010. The specimens were taken from either crown lengthening procedures or distal wedge periodontal surgeries. After being stored in an alpha modification of Eagle’s medium (α-MEM) (Invitrogen, Grand Island, NY, USA) with 10% qualified fetal bovine serum (FBS) (Invitrogen) and 1% penicillin, streptomycin (P/S), the specimens were immediately transported to the laboratory. In the present experiments, all of the procedures had been approved by the Ethics Committee of the Faculty of Medicine, Tri-service General Hospital, Taipei, Taiwan (TSGHIRB-100-05-099) and all participants gave their informed consent.
Colony forming unit assay
The efficiency of hGMSCs in forming colonies was detected with a colony forming unit (CFU) assay. P0 cells were plated at 5,000 cells/10 cm dish and P4 cells were plated at 500 cells/10 cm dish. After being cultured for 14 days, they were fixed and stained with crystal violet. The number and size of the colonies, containing 50 or more cells, were recorded. The colony forming rate was then calculated as the number of colonies formed per hundred cells.
Telomerase activity assay
To examine the cell proliferation capability of hGMSCs, a telomerase activity assay was carried out. The telomerase activity of hGMSCs was measured with 1.5 μg of protein extracts using a TRAPEZE® Telomerase Detection Kit (S7700, Merck Millipore Headquarters, Billerica, MA, USA), and the protein concentration was determined with a BCA™ Protein Assay Kit (Thermo Fisher Scientific Inc., Waltham, MA, USA). TRAP assay products were separated on a 10% polyacrylamide gel following staining with SYBR® Safe staining (Invitrogen) and were visualized with a camera system (ChemiDoc XRS + system, Bio-Rad Laboratories, Hercules, CA, USA). The gel images were scanned directly with software (Image Lab, Bio-Rad Laboratories) and quantitated according to the kit instructions.
Flow cytometry for surface marker analysis
To determine the expression of the conventional surface markers used to define hMSCs (CD73, CD90 and CD105) and stromal stem cells (STRO-1) on hGMSC, they were examined by flow cytometry. The hGMSCs were prepared as single cell suspensions by trypsinization and resuspended in blocking buffer containing Hank’s balanced salt solution (Sigma–Aldrich Inc.) supplemented with 1% bovine serum albumin (BSA; Sigma–Aldrich Inc.) for 30 minutes. Approximately 1 × 106 cells/mL were incubated with phycoerythrin (PE)- or fluorescein isothiocyanate (FITC)-conjugated monoclonal antibodies against CD73 (BD Biosciences, San Jose, CA, USA), CD90 (eBioscience, San Diego, CA, USA), CD105 (eBioscience) and STRO-1 (Santa Cruz Biotechnology, Santa Cruz, CA, USA, ) for 30 minutes at 4°C in the dark, then rinsed and kept in Hank’s balanced salt solution with 1% BSA on ice until analysis. Samples were analyzed using a FACSCalibur flow cytometer (Beckman Coulter, Hialeah, FL, USA). Data were processed using FCS Express V3 software (Beckman Coulter).
Osteogenic, adipogenic, neural differentiations of hGMSCs
Osteogenic differentiation was induced after the hGMSCs were seeded at a density of 1 × 104 cells/well on 12-well culture plates in α-MEM with 5% FBS and 1% P/S. When cells reached 80% confluence, the medium was changed to osteogenic medium which contained α-MEM with 5% FBS, 1 nM dexamethasone (Sigma-Aldrich Inc.), 50 μM L-ascorbic acid 2-phosphate sesquimagnesium salt (Sigma-Aldrich Inc.), 20 mM β -glycerophosphate (Sigma-Aldrich Inc.) and 50 ng/mL L-thyroxine sodium pentahydrate (Sigma-Aldrich Inc.). The medium was changed twice a week for three weeks for osteogenic induction. After being fixed with 4% paraformaldehyde, the culture was stained with 1% Alizarin Red S at pH 4.1 for 20 minutes.
For adipogenic differentiation, 1 × 104 cells/well were seeded on 12-well culture plates. When the cells reached 80% confluence, the medium was changed to adipogenic medium which contains α-MEM with 5% FBS, 1 μM dexamethasone, 50 μM indomethacin (Sigma-Aldrich Inc.), 5.0 μg/mL insulin (Sigma-Aldrich Inc.) and 0.5 μM 3-isobutyl-1-methylxanthine 3-isobutyl-1-methylxanthine (IBMX, Sigma-Aldrich Inc.). Then the medium was changed twice a week for four weeks for adipgenic induction. After fixation, the culture was stained with 0.0125% Oil red O (Sigma-Aldrich Inc.) in isopropanol for 20 minutes.
For neural differentiation, 1 × 104 hGMSCs/well were seeded on poly-L-lysine/laminin-coated eight-well multiple-chamber slides (Merck Millipore) in Dulbecco’s modified Eagle’s medium/F12 (DMEM/F12) (InvitroGen) supplemented with 125 ng/ml basic fibroblast growth factor (bFGF) (InvitroGen), 1,000 unit/ml leukemia inhibitory factor (Sigma-Aldrich Inc.) and 4 mM forskolin (Sigma-Aldrich Inc.). After three to approximately seven days, the cells were fixed with 4% paraformaldehyde for immunocytochemistry staining.
EMD treatment, the cell proliferation assay and osteogenic differentiation
To evaluate the effects of EMD on the proliferation of hGMSCs, 1 × 104 cells were cultured in a well containing 10% FBS in α-MEM media (Invitrogen Corporation, Carlsbad, CA, USA) to 70% confluence in a 96-well plate, and the medium was changed to serum-free α-MEM (InvitroGen, Grand Island, NY, USA) to starve the cells overnight. The cells were then treated with 0, 25 or 100 μg/ml of EMD (Emdogain®; Straumann AG, Basel, Switzerland) for 24 hours or 48 hours. The proliferation of hGMSCs was measured at OD 490 nm using the CellTiter 96® AQueous One Solution Cell Proliferation Assay (MTS, Promega, Madison, WI, USA). All the experiments were repeated three times.
To examine the osteogenic effects of EMD on hGMSCs, the stem cells were cultured at a density of 1 × 104 cells/well in 12 well culture plates and 1 × 103 cells/well in eight-well chamber slides (Merck Millipore) in α-MEM with 5% FBS and 1% P/S (Invitrogen) until 70% confluence. The cells were treated with a mineralization solution (50 μM ascorbic acid, 10 nM dexamethasone and 20 mM β-glycerophosphate) (Sigma-Aldrich) either in the absence of EMD (control cultures) or in the presence of EMD (25 μg/ml or 100 μg/ml). Then, the medium was changed twice a week. After one, two, three or four weeks of cultivation in each treatment, hGMSCs were washed with PBS and fixed with 4% paraformaldehyde (Sigma-Aldrich). The cultured cells in the 12-well culture plate were stained with Alizarin red S (ARS) (Sigma-Aldrich) following routine procedures. Later, 0.5 N HCl and 5% sodium dodecyl sulfate were added to each well to dissolve the stained nodules. The light absorbance of the extracted dye was measured with a microplate spectrophotometer (Thermo Fisher Scientific) at 405 nm as previously described . The cultured cells in the eight-well chamber slides were used for immunocytochemistry staining.
Reverse transcription polymerase chain reaction and real-time PCR
To explore the expressions of osteogenic genes, hGMSCs were seeded at a density of 1 × 105 cells/well in six-well culture plates, and the effects of different concentrations of EMD on gene expression were observed. The treatment conditions were identical to those of the osteogenic differentiation.
After various times (including 3, 6, 12, 24 or 72 hours) of cultivation and treatment with EMD or not, RT-PCR was performed to evaluate the semi-quantity of gene expression in alkaline phosphatase (ALP) and osteocalcin (bone γ-carboxyglutamate (Gla) protein; OC). To measure the mRNA expression of ALP and OC after osteogenic treatment with or without EMD, total RNA was extracted using TRIsure reagent (Bioline Ltd., London, UK). As described previously  with slight modification, 1 μg of total RNA was reverse transcribed with Tetro RT enzyme (Bioline Ltd.) into cDNA, and used as the template for PCR reactions and analysis.
Transcribed cDNA was then amplified using the QuantiTect Primer Assay gene expression assay, including QT00020517 for Cbfα-1, QT00012957 for ALP, QT00232771 for OC and QT01192646 for the endogenous control glyceraldehyde-3-phosphate dehydrogenase (GAPDH) according to the manufacturer’s instructions using a Rotor-Gene cycler (QIAGEN, Hilden, Germany). Gene expression for human ameloblastin (AMBN), forward 5′-GAGTTTTGCAGTGCCGTTCT-3′ and reverse 5′-CTGCAGACTTCCCAACTGTCT-3′ (NM_016519.5) was also determined. Calculations of relative gene expressions (normalized to GAPDH reference gene) were performed according to the 2-ΔΔCT method .
Alkaline phosphatase enzyme activity assay
We also addressed osteogenic differentiation of hGMSCs by measuring ALP activity in culture. hGMSCs were cultured as described above, either without EMD (control group) or with EMD (25 μg/ml or 100 μg/ml). On day 3 and day 5, the cells were washed in PBS and scraped in 10 mM Tris–HCl buffer (pH = 7.6) containing 10 mM MgCl2 and 0.1% Triton X-100. ALP activity was determined colorimetrically with p-nitrophenyl phosphate as a substrate. Then, the protein content was measured by a Pierce BCA Protein Assay kit (Thermo Fisher Scientific) with the use of a microplate spectrophotometer at 405 nm and BSA as the standard. Enzyme activity was shown as Units/mg protein.
Immunocytochemistry and confocal laser scanning microscopy
hGMSCs in eight-well chamber slides (Merck Millipore) were used for immunocytochemistry. After fixation with 4% paraformaldehyde, cells were permeabilized with methanol, blocked with 5% BSA in PBS for 20 minutes, and then exposed to the primary antibody of nestin, microtubule-associated protein 2 (MAP-2), glial fibrillary acidic protein (GFAP) (Merck Millipore), cbfα-1 (Abcam, Cambridge, UK), or OC (Epitomics Inc., Burlingame, CA, USA) overnight at 4°C. The cells were washed in PBS, exposed to the secondary antibody of FITC-conjugated goat anti-rabbit immunoglobulin G (IgG) (Abcam) or Alexa Fluor 568-conjugated goat anti-mouse IgG (InvitroGen) for 30 minutes and counterstained with 4',6-diamidino-2-phenylindole (DAPI). The nuclear translocation of cbfα-1 and protein expressions of nestin, MAP-2, GFAP and OC in hGMSCs were observed by confocal laser scanning microscopy (LSM780, Carl Zeiss MicroImaging, Inc., New York, NY, USA).
One-way analysis of variance (ANOVA) was selected to evaluate the differences in the expression of mRNA for Cbfα-a, ALP and OC between hGMSCs treated with EMD (0, 25 or 100 μg/ml) for various times. Duncan’s test was used for post-hoc analysis, and P <0.05 was deemed to be significant.
The stem cells could be successfully isolated from gingiva
The cell colonies could be easily identified after staining with crystal violet (Figure 1b left). At P0, the mean colony formation rate was 1.4%; however, a significantly increased colony formation rate was observed at P4 (mean = 15.9%) (Figure 1b right). Significantly higher telomerase activities, indicating a higher activity of cell renewal, were observed in hGMSCs when compared with the activity from gingival fibroblasts (Figure 1D). The isolated cells at P4 expressed high levels of surface markers for CD73, CD90 and CD105, but a low expression was observed for STRO-1 (Figure 1C). Multi-potency in osteogenic, adipogenic, and neural differentiation of the isolated hGMSCs was successfully induced (Figure 1E).
Effect of EMD on the cell proliferation and osteogenic differentiation of hGMSCs
Effect of EMD on gene expressions of hGMSCs during osteogenic differentiation
Effect of EMD on the protein expression of hGMSCs during osteogenic differentiation
Using confocal laser scanning, increased protein expression of cbfα-1 after the EMD treatments could be observed at day 1 and nuclear translocation could be clearly observed at day 3 (Figure 3A). Increased protein expression of OC was observed at weeks 3 and 4 after the EMD treatments, especially at the 25 mg/mL concentration at week 4 (Figure 3B). Increased activities of ALP were observed at days 5 and 7 after EMD treatment (Figure 3C).
The discovery of stem cells and recent progress in stem cell biology has made a great contribution to the development of regenerative therapeutic strategies for multiple diseases. Generally, there are two major properties of stem cells: they are capable of both self-renewal and differentiation upon division . The aim of the present study was to investigate the effects of EMD on the proliferation and mineralization of GMSCs. Our isolated human gingival cells had an increased colony forming rate, high telomerase activity, high levels of common MSC markers (for example, CD73, CD90 and CD105) and multi-potency in differentiation (Figure 1). Therefore, we suggest that the cells isolated in this study have the characteristics of MSCs. In the present study, the hGMSCs are adult mesenchymal stem cells, which are the general cell types of the tissue near where they reside. The application of adult stem cells in research and medical therapies is less controversial than embryonic stem cells because these cells can be harvested and isolated without destroying an embryo . In addition, adult stem cells can be found almost throughout all body tissues, including dental tissues , although the proliferative potential and the differentiation capacity of adult stem cells, such as the periodontal ligament stem cells, decrease as age increases .
Previous in vitro and in vivo studies have shown that EMD promotes the regeneration of periodontal tissues and affects the proliferation and mineralization of cells, such as cementoblasts and periodontal ligament cells [28–34]. EMD also promotes the regulation of osteoclastogenesis, the proliferation and migration of periodontal cells, and also stimulates the signal transduction of bone morphogenic protein and transforming growth factor-β [31, 35–40]. In addition, the properties of EMD are like those of the extracellular matrix protein which guide or regulate the proliferation, migration and differentiation of osteoblasts [28, 30–32]. An in vitro study with DNA microarrays has shown that EMD is able to modulate a broad range of osteoblast biologic activity genes, such as cell cycle regulation, proliferation, apoptosis, cytoskeleton, cell adhesion, extracellular matrix production and vesicular transport in ostoeoblast cultures . A recent study in a mouse preosteoblast cell line also showed that EMD increased the mRNA expression of bone sialoprotein and osteopontin, the phenotypic markers of osteoblastic differentiation; as a result, it accelerates and improves matrix mineralization . In another study of human bone marrow stromal cells, EMD affected cell proliferation positively while decreasing the osteogenic differentiation .
OC is a specific late marker of osteogenic differentiation, indicating the major non-collagenic protein of the bone matrix. OC plays important regulatory functions in the bone-remodeling process, and its levels usually proceed in parallel with the final event of matrix mineralization [44, 45]. In our present study, EMD significantly stimulated OC expression at all of the time points at the high dose (100 μg/ml) (Figure 3C). This finding was consistent with the increased mineralization of extracellular matrix after EMD treatment. OC was a matrix signal for bone formation, stimulating differentiation of osteoblasts.
In the present study, EMD not only enhanced the osteogenic differentiation of hGMSCs but also promoted the proliferation of hGMSCs (Figure 2a). In osteogenesis, the cell cycle progression of the osteoblast is arrested and, hence, increases its differentiation [23, 46]. However, the proliferation of progenitor cells usually occurred at the early stage before the differentiation starts [47, 48]. In the present study, different media were used for cell proliferation and mineralization. In the experimental hGMSC proliferation, the medium was not suitable for osteogenic differentiation and the observation period was limited to no more than 48 hours (which is at the early stage of cell proliferation). Furthermore, in the osteogenic differentiation experiment, an osteogenic medium was used and the observation period was much longer than in the proliferation experiment. As a result, hGMSCs were treated with EMD in different culture media that enhanced either proliferation or osteogenic differentiation.
Our data demonstrate that hGMSCs could be successfully isolated from human gingiva, and EMD treatment could promote not only the proliferation but also the mineralization of these isolated hGMSCs.
bovine serum albumin
core binding factor alpha
enamel matrix derivative
fetal bovine serum
glial fibrillary acidic protein
gingiva-derived mesenchymal stem cells
This study was partly supported by grants from the National Science Council, Taipei, Taiwan (NSC-101-2314-B-016-034), Tri-Service General Hospital (TSGH-C101-038) Tri-Service General Hospital (TSGH-C102-032) and the C. Y. Foundation for Advancement of Education, Sciences, and Medicine, ROC.
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