- Open Access
Human placenta-derived mesenchymal stem cells ameliorate orbital adipogenesis in female mice models of Graves’ ophthalmopathy
Stem Cell Research & Therapy volume 10, Article number: 246 (2019)
Graves’ ophthalmopathy (GO) is a complication of Graves’ disease (GD), in which orbital connective tissues become inflamed and increase in volume and orbital fibroblasts within the orbital fat and extraocular muscles differentiate into adipocytes in vitro when stimulated by hormones, several cytokines, and growth factors including TSH, IGF-1, IL-1, interferon γ, and platelet-derived growth factor. Human placental mesenchymal stem cells (hPMSCs) have immunomodulatory effects in disease pathogenesis. Although a number of studies have reported that hPMSCs can elicit therapeutic effects, these are not sufficient. Therefore, we constructed a GO animal model in order to find out the hPMSCs recovery effect.
We investigated their anti-adipogenic effects in in vitro cultures of orbital fibroblasts established from GO patients. Primary orbital fibroblasts were exposed to differentiation medium for 10 days. After being co-cultured with hPMSCs, the characteristics of orbital fibroblast were determined by Oil Red O stain and real-time PCR. Then, we explored the in vivo regulatory effects of hPMSCs in an experimental mouse model of GO. We developed the GO mouse model using immunization by leg muscle electroporation of pTriEx1.1Neo-hTSHR A-subunit plasmid. Human PMSC injection was performed into the left orbit. We also analyzed the effects of hPMSCs in the GO animal model.
We found that hPMSCs inhibited a lipid accumulation and activated factors, such as ADIPONECTIN, PPARγ, C/EBPα, and TGFβ2 genes in adipogenesis-induced primary orbital fibroblasts from GO patients. Moreover, hPMSCs were highly effective at ameliorating adipogenesis in the orbital tissue of the model.
These data indicate that hPMSCs recover pathogenic activation of orbital fibroblasts in animals undergoing experimental GO and confirm the feasibility of applying hPMSCs as a novel treatment for GO patients.
Graves’ disease (GD) is an autoantibody-induced immune disorder related to the thyroid-stimulating hormone receptor (TSHR) in the thyroid gland, causing toxic goiter or hyperthyroidism . Graves’ ophthalmopathy (GO) is an autoimmune inflammatory disorder in which TSHR-stimulating antibody and TSHR influence several different cells in the periorbital tissue . GO patients see the medical doctors for the thyroid eye manifestations as the first noticeable warning signs at the onset of the disease; otherwise, they could complicate the progression of the disease . The typical thyroid eye features include proptosis, eyelid retraction, exposure keratopathy, restrictive strabismus, limitation of eye movement, compressive optic neuropathy, and appearance disfigurement. T cell infiltration and fibroblastic glycosaminoglycan accumulation are the main pathologies of the autoantibody-mediated inflammatory and fibrotic events in the periorbital fat and extraocular muscles (EOMs). Edematous swelling of the EOMs and adipogenesis of orbital fat lead to an increase of the volume within the bony orbital pyramid, and the common GO symptoms are followed such as irritation, orbital pain, tearing, diplopia, vision loss, corneal ulceration, and even blindness . The major medical treatment methods to modify the disease course are high-dose steroids and radiation therapy. High-dose corticosteroids are effective in about 65% of patients. However, the total amount of corticoid use is restricted for the systemic adverse effects, including hyperglycemia, hypertension, and immune system compromise, and the eye symptoms usually recur when the steroid treatment is tapered or withdrawn [4,5,6]. Radiation therapy is another popular modality for the treatment of GO and is considered to treat the patients who are resistant to or cannot tolerate the side effects of corticoids. But the side effects of radiation therapy should also be kept in mind such as keratitis sicca, cataracts, and retinopathy [7, 8]. A number of advanced therapies have been introduced, most of which have studied about immunomodulatory effects; these include rituximab (RTX), tocilizumab (TCZ), the humanized anti-interleukin-6 receptor monoclonal antibody, teprotumumab, IGF-1 receptor-blocking antibodies, and TNF-α inhibitors [9, 10].
Human placental mesenchymal stem cells (hPMSCs) are the cells with self-renewing abilities originated from human placenta that can differentiate into multiple lineage cell types. Various studies have reported that hPMSCs can elicit therapeutic effects via differentiation and/or secretion of factors such as growth factors, cytokines, and chemokines . hPMSCs contribute to the repair of tissue damage caused by ischemic diseases including strokes, myocardial infarctions, and cerebral infarctions [12,13,14]. Furthermore, in the field of ophthalmology, cryopreserved amniotic membranes and their by-products have been recognized as significant tools for the treatment of ulceration and epithelial defects over the past 20 years [15, 16]. Recently, a number of translational studies have reported that the anti-inflammatory effects of hPMCSs can be used to modulate chronic diseases such as Crohn’s disease, multiple sclerosis, and sarcoidosis [17,18,19]. In this study, we investigated the immunomodulatory effects of hPMSCs in the case of GO using both in vitro tests with orbital fibroblast (OF) cultures and in vivo tests and compared our results with those of conventional steroid treatments in an experimental mouse model of GO [20, 21].
Materials and methods
Orbital fibroblast preparation
Orbital adipose tissue explants were obtained from three GO patients during orbital fat decompression and three control individuals with no history of GO during blepharoplasty. The process of obtaining orbital adipose tissue was approved by the Institutional Review Board of Bundang CHA Medical Center (Seongnam-si, South Korea), and consent was obtained from all patients. Tissue explants were chopped and treated with collagenase (0.25 mg/mL; Thermo Fisher Scientific, Waltham, MA, USA) for 1 h at 37 °C in a shaking incubator. After digestion, the tissues were placed directly in culture dishes with DMEM/F12 containing 20% fetal bovine serum (FBS; Thermo Fisher Scientific) and 1% penicillin/streptomycin (Thermo Fisher Scientific). The cells were serially passaged, and the results of the fifth to eighth cell passages were used for the experiments.
Human placenta stem cell preparation
We previously described the methods for preparing hPMSCs . The collection and use of the samples were approved by the Institutional Review Board of CHA General Hospital (Seoul, South Korea). All of the participants provided written informed consent prior to the sample collection. Briefly, the placentas were collected from mothers who were free of medical, obstetric, and surgical complications who delivered at term (> 37 gestational weeks). The hPMSCs were collected from the inner side of the chorioamniotic membrane of the placenta and then treated with 0.5% collagenase IV (Sigma-Aldrich, St. Louis, MO, USA). Human PMSCs were cultured in Minimum Essential Media (MEM) alpha GlutaMAX (Thermo Fisher Scientific) supplemented with 10% FBS (Thermo Fisher Scientific), 1% penicillin/streptomycin (Thermo Fisher Scientific), 25 ng/mL human fibroblast growth factor 4 (Peprotech, Inc., Rocky Hill, NJ, USA), and 1 μg/mL heparin (Sigma-Aldrich).
Human orbital fibroblasts (hOFs) (3 × 105) derived from either fresh cultures or frozen cells were seeded in a 6-well plate and incubated until they reached the desired confluence. For all experiments, OFs derived from GO patients were grown together with OFs from normal individuals as controls. To obtain confluent cultures, adipogenesis was induced by replacing the culture medium with DMEM supplemented with 10% FBS, 1% penicillin/streptomycin, 33 μM biotin, 17 μM pantothenic acid, 0.2 nM T3, 10 μg/mL transferrin, 0.2 μM prostaglandin I2, 0.1 mM isobutylmethylxanthine (IBMX), 1 μM dexamethasone, and 1 μM insulin (Sigma-Aldrich). The differentiation-induced medium was replaced every day for 4 days. Thereafter, the medium was changed to differentiation medium lacking IBMX, dexamethasone, and insulin, and the cells were cultured for up to 8 days more, after which Transwell cell culture plate insert was put on 6-well plate. Then, hPMSCs (3 × 105) were seeded into the insert membrane. After 48 h, the co-cultures of OFs and hPMSCs were used for experimentation, as described below.
Oil Red O staining
After 10 days of adipocyte differentiation, cells were stained with Oil Red O. The working solution was prepared by diluting 6 mL stock solution (0.5% Oil Red O in isopropanol) in 4 mL distilled water. After washing with DPBS, cells were fixed in 10% formaldehyde solution for 1 h at room temperature (RT). After fixation, the cells were washed with distilled water and stained with Oil Red O solution for 30 min at RT. After washing with distilled water, stained cells were visualized under a microscope. To quantify lipid accumulation, 100% isopropanol was added into the stained well. Then, the optical density was measured using a spectrophotometer at 490 nm.
Quantitative reverse transcription polymerase chain reaction analyses
Total RNA was isolated from hOFs using TRIzol reagent (Ambion, Carlsbad, CA, USA). Quantitative real-time PCR (qPCR) was performed with IQ SYBR Green Supermix (Bio-Rad Laboratories, Hercules, CA, USA). We quantified the gene expression using the delta CT method, and qPCR reactions were performed using a CFX-96 machine (Bio-Rad Laboratories). The nucleotide sequences of all primers used are presented in Table 1.
Development of an experimental mouse model of GO using female BALB/c mice
We developed a GO mouse model using immunization by leg muscle electroporation of pTriEx1.1Neo-hTSHR A-subunit plasmid as previously described . BALB/c female mice (age 6 weeks) (Orient Bio Inc., Gyeonggi-do, South Korea) were housed in a standard animal facility, with food and water provided ad libitum at a constant temperature of 21 °C. The animals were maintained in an air-conditioned animal house under specific pathogen-free conditions. The animal protocol was approved by the Institutional Animal Care and Use Committee of CHA Bundang Medical Center. We injected 50 μL plasmid (1 mg/mL in BSS PLUS Irrigating Solution) into the leg muscles of BALB/c female mice (age 6 weeks), followed by electroporation using an ECM 830 system (BTX Harvard Apparatus, Holliston, MA, USA). Electroporation was performed at 200 V/CM and 10–20 ms square wave pulses. Injection and in vivo electroporation were performed four times, at 3-week intervals. After the 13-week immunization period, we injected the mice with BSS, hPMSCs, and steroids.
At 22 weeks after the first immunization (Fig. 1a), all of the immune animals were bled to evaluate the induced anti-TSHR antibodies. The hyperthyroid animals undergoing experimental GO were divided into the following groups: a treatment group injected with hPMSCs (n = 14; 3 × 105 cells/30 μL), a treatment group injected with steroids (n = 14; 0.4 mg each, triamcinolone acetonide, Dongkwang Pharmaceutical Co., Hanmi, South Korea), and a sham group (n = 12; 30 μL BSS PLUS). An intra-orbital injection was performed into the left orbit. After single hPMSC injection, the animals were sacrificed after 1, 2, or 4 weeks, after which their blood was collected for serum, and orbital tissue was excised for histopathological analyses.
Measurement of antibodies to TSHR
We confirmed that GO animal models had been achieved before dividing the mice into treatment groups based on the analyses of their serum at 21 weeks using the anti-TSH receptor antibody (TRAb) from the Fast ELISA commercial kit (EUROIMMUN, Luebeck, Germany). We used the antibodies as indicated by the manufacturer’s instructions. The results are expressed as the percentage inhibition of labeled M22 binding to the immobilized TSHR in the plate wells.
Measurement of cytokines in the blood
The levels of pro- and anti-inflammatory cytokines in the serum of immune mice were determined using the Magnetic Luminex® Screening Assay (Thermo Fisher Scientific), according to the manufacturer’s instructions. The values were measured using Luminex 100 (Luminex, Austin, TX, USA). The following cytokines were measured: IL-1β, IL-2, IL-4, IL-6, IL-10, TNFα, ICAM-1, G-SCF, and GM-CSF.
In vivo orbital magnetic resonance imaging
Immune animals with GO (n = 2) and age-matched normal mice (n = 1) were evaluated via magnetic resonance imaging (MRI) using the 4.7 T MRI system (BioSpec 47/40; Bruker, Ettlingen, Germany) at the Korea Basic Science Institute. To acquire in vivo MR images, the animals were anesthetized with inhaled isoflurane (5% induction, 1.5% maintenance) at a O2–N2O (3:7) mixture, and their body temperatures were maintained at 37 ± 1 °C. Anesthesia was induced and maintained by administering a 1–2% isoflurane–oxygen mix throughout the imaging process. The head of each mouse studied was situated within an MRI volume coil with an internal diameter of 25 mm. Axial T2-weighted MR images were acquired using a rapid acquisition with relaxation enhancement (RARE) sequence with the following settings: repetition time (TR), 4 s; effective echo time (TE), 33 ms; echo train length, 8; field of view (FOV), 20 mm × 20 mm; and matrix size, 256 × 256 (50 μm in-plane resolution). The ImageJ software application (NIH) was used to view the MR images and measure the orbital volume of the left eye. After confirming the regional volume differences between the controls and GO models via MRI, another three GO animals were treated with hPMSCs, steroids, or injected BSS. Four weeks later, we conducted MRI analyses of these immunized mice.
Orbital and thyroid tissue histopathology
Quantification of the adipose tissue around the optic nerve was conducted using Image J. The cross-sectional area of the orbital fat was normalized to the optic nerve area of each mouse. The adipose areas of the orbital sections of each mouse were evaluated in every group.
Immunoblot analyses of target proteins and cell signaling pathways
Lysates were prepared from orbital tissues, which were injected with BSS (sham), hPMSCs, or steroids by homogenization with PRO-PREP solution (Intron, Gyeonggi-do, South Korea). Equal amounts of total protein were resolved by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and transferred to the membranes. The membranes were immunoblotted with anti-ICAM-1 (Thermo Fisher Scientific), TGFβ1, TGFβ2 (GeneTex, Irvine, CA, USA), TNF-α (Thermo Fisher Scientific), TSHR (NSJ Bioreagents, San Diego, CA, USA), phosphorylated ERK (p-ERK), total ERK, AKT (Cell Signaling Technology, Denver, MA, USA), mTOR (Thermo Fisher Scientific), or α-tubulin (GeneTex). After washing, the membranes were incubated at RT for 2 h with horseradish peroxidase-conjugated anti-rabbit or mouse IgG secondary antibodies at a dilution of 1:5000 (GeneTex). Immunoreactive bands were visualized with enhanced chemiluminescence solution (Bio-Rad Laboratories, Hercules, CA, USA) and detected using an ImageQuant LAS 4000 (GE Healthcare Life Sciences, Little Chalfont, UK).
Engraftment of hPMSCs
We confirmed the presence of injected hPMSCs in orbital tissues by analyzing them in two ways. (1) The tissues from each group were embedded in OCT compound. After making slide sections, DAPI staining was performed. Fluorescence was detected using a fluorescence microscope. (2) cDNA was synthesized using orbital tissues. Expression of the human-specific gene chorionic somatomammotropin hormone 1 (CSH1) was detected in cDNA extracted from tissues injected with hPMSCs. The primers used are presented in Table 1.
Data analyses were conducted using GraphPad Prism (GraphPad Software, La Jolla, CA, USA). Statistically significant differences were identified using a t test or nonparametric statistical test, followed by Mann-Whitney U test at a significance level of 5%.
To investigate the therapeutic function of hPMSCs, we established an experimental mouse model of GO as described in a recent study . Human TSHR A-subunit plasmid was delivered to mice by electroporation (Fig. 1a). In a TSH-binding inhibitory immunoglobulin (TBII) assay using an anti-TSH receptor (TRAb) ELISA, the GO models exhibited > 78% inhibition of labeled TSH binding activity compared to the control group (Fig. 1b). The orbital region of the animals was examined using small animal MRI and was compared to the orbital region of age-matched control mice. The orbital volumes measured from the MR images increased by 20–30% compared to the age-matched controls (Fig. 1c). Human PMSCs decreased by > 20% in the orbital volume around the eyes of GO mice immunized with hTSHR A-subunit plasmid. Steroids also had a similar efficacy at reducing the orbital volume (Fig. 1d).
Next, we assessed the pathology of the GO groups. We used hemotoxylin and eosin staining to measure the volume of orbital tissues in each group. At 2 weeks post-transplantation, the retrobulbar adipose tissue of the hPMSC-injected mice showed a significant reduction in the pathologic expansion (Fig. 2a). Furthermore, although disease expansion also decreased in tissues injected with hPMSCs and steroids, the reductions were not significant (Fig. 2a).
Engraftment of hPMSCs
We confirmed the infiltration of injected hPMSCs by assessing the eye orbital tissues and liver samples. We confirmed the mRNA expression of human CSH1, which is highly expressed in the placenta. Hence, the hPMSCs remained successfully engrafted by our procedure (Fig. 2b). As a negative control, we could not find hCSH1 band in liver tissues (Fig. 2b). We also observed PKH67-labeled green fluorescent cells in local regions surrounding the sites injected with hPMSCs at 1 week, further supporting the successful engraftment of stem cells (Fig. 2c).
Human PMSCs attenuate pro-inflammatory cytokines
We also investigated whether hPMSCs could reduce the inflammatory response in GO disease models by measuring their concentration in serum samples. As shown in Fig. 3, sham GOs presented a significantly higher level of various anti- and pro-inflammatory cytokines than normal mice, IL-6, TNFα, IL-4, and GM-CSF at 1 week; IL-6, IL-4, IL-4, and IL-10 at 2 weeks; and IL-4 and IL-10 at 4 weeks. Compared with the sham GOs, serum from hPMSC-injected GO models contained similar levels of cytokines with age-matched sham, but that from steroid-injected GO presented reduced level of ICAM-1 at 1 week and GM-CSF at 2 weeks and 4 weeks (Fig. 3).
Human PMSC transplantation decreases candidate target protein expression in the GO animal model
We investigated the target protein expression in the orbital tissues of the GO animal models. The expressions of TSHR, TGFβ2, ICAM-1, and TNFα significantly decreased following treatment with hPMSC or steroid injections. Specifically, hPMSCs significantly reduced the levels of the target protein at 1 week post-transplantation. Steroids affected TSHR and ICAM-1 up to 4 weeks post-transplantation (Fig. 4a).
Human PMSCs attenuate target protein levels in GO animal models via the p-AKT and ERK signaling pathways
As shown in Fig. 4a, hPMSCs reduced the levels of some target proteins. Thus, next, we investigated the signaling pathways involved in regulating the target proteins by assessing the general signal relative to protein expression. We observed less p-AKT, p-mTOR, and p-ERK expression in the treatment injection groups (Fig. 4b). Moreover, steroids inhibited the activation of p-AKT, p-mTOR, and p-ERK longer than hPMSCs (Fig. 4b).
Human PMSCs inhibit lipid accumulation by regulating adipogenic factors
The effects of hPMSCs on lipid accumulation in hOFs are presented in Fig. 5a. After adipocyte differentiation, we observed Oil Red O-stained adipocytes in OFs collected from GO patients and normal. Lipid accumulation in differentiated fibroblasts was decreased by co-culturing with hPMSCs. To understand the molecular mechanisms underlying the inhibition of lipid accumulation, we evaluated the gene expression involved in lipid biosynthesis. The effects of hPMSCs on the differentiation of adipose fibroblasts were investigated by qPCR analyses (Fig. 5b). As expected, in fibroblasts co-cultured with hPMSCs, ADIPONECTIN, PPARγ, C/EBPα, and TGFβ2 mRNA levels were significantly decreased compared to the cells that were not co-cultured. This suggests that hPMSCs regulated adipogenic factors and clearly indicates that hPMSCs inhibited the accumulation of lipids in OFs from GO patients.
GO is a complication of GD, but mechanistic insights into its pathogenesis are lacking, which have been hampered by the lack of an animal model. The TSHR and perhaps IGF-1 receptor are considered to be relevant antigens [10, 23]. Deficient immune tolerance to THSR contributes to the development of GO . The activation of T cells and autoantibodies to TSHRs are related to the pathogenesis of TAO [10, 24]; however, the details of this process remain unclear. GO is caused by an inflammatory process that increases the volume of extraocular muscle (EOM) and causes histological changes in orbital tissues . Recently, to investigate the pathogenesis of GD, a number of studies based on mouse models have been reported [26, 27]. OFs from GO patients have also been characterized [28,29,30]. Several studies have provided experimental evidence that OFs derived from retrobulbar fat of GO patients have similar immunophenotypic features and differentiation abilities as MSCs but differ in terms of their immunosuppressive potential [28, 29]. Furthermore, comparative analyses of adipose-derived MSCs from GO orbital fat and abdominal fat have been conducted to understand the phenotypic characteristics of OFs in GO patients .
However, it is not sufficient to understand the complexities of the orbital remodeling process. In previous studies, we observed that genetic immunization by injection of human TSHR A-subunit plasmid led to the remodeling of orbital tissue, recapitulating the pathological features of GO [20, 21]. In those studies, orbital pathology was characterized in terms of the interstitial inflammation of EOMs with CD3+ T cells and F4/80+ macrophages, adipogenesis, and fibrosis. In addition, in vivo MRI scans of the orbital regions of mice have provided clear and quantifiable evidence of orbital muscle hypertrophy with protrusion (proptosis) of the eye . MR imaging can be applied to diagnose GO and assess patient responses to treatment [31, 32]. GO animal models exhibit IL-10, IL-6, and TNF-α cytokine responses to activated T cells .
Despite the fact that there have been a number of studies on GO pathogenesis, there are not yet definite diagnostic criteria or therapeutic treatments for GO. A number of treatments for specific therapeutic targets have been reported. The applicability of a particular treatment for GO depends on the severity and activity of TAO. For patients with mild, active TAO, short courses of oral glucocorticoids and/or anti-inflammatory agents may be sufficient . In the case of moderate to severe and active TAO, nonspecific anti-inflammatory agents are commonly used. However, systemic corticosteroids are administered in some cases . Because glucocorticoids are associated with the risk for adverse events, various treatments have been developed for specific targets. Teprotumumab (a repurposed IFG-IR inhibitor), rituximab (anti-CD20), B cell-depleting agents, and tocilizumab may be candidate treatments for the treatment of advanced TAO [10, 32]. Furthermore, low-dose radiotherapy (LD-RT) has been considered an alternative to treatment with systemic anti-inflammatory reagents. This induces an inflammatory response in irradiated tissues, thus producing an anti-inflammatory effect . The response to LD-RT is regulated by a sequence of interactions between leukocytes and the endothelium. The mechanisms governing this response include decreased leukocyte-endothelial cell adhesion, induction of cell death by inflammatory infiltration, and decreased expression of adhesion molecules (P-, L-, E-selectins, ICAM-1, VCAM-1) [32,33,34].
Three types of TSHR monoclonal antibody (stimulating, blocking, and cleavage antibodies) have different functional capabilities in GD patients . M22, a widely used and high-affinity stimulating human mAb to TSHR, is considered an international standard . Stimulating antibodies induce thyrocyte cell survival and proliferation via cAMP/PKA/CREB and Akt/mTOR/S6k signaling. On the contrary, cleavage antibodies result in apoptosis via ROS induction and NF-κb activation. The balance between negative and positive regulations may be important for maintaining thyrocyte homeostasis in GD .
In a previous study, we investigated that NF-κb could be the mediator protein in the hPMSC-related recovery pathway . Transactivation of NF-κb protein would take an important part in the recovery process from hypoxic damage. We also found out that hPMSCs could upregulate the expression of axon survival-related genes and support recovery from optic nerve compression. This helped us understand the potential role of hPMSCs as a treatment modality for the traumatic optic nerve injury . Immunomodulatory properties of cultured MSCs were discussed that they could directly suppress the proliferation of T cells in vitro [37,38,39] and also avoid cytotoxic T cell-mediated lysis . Furthermore, they can both inhibit  and promote  B cell proliferation, hinder NK cell activation [43, 44], and control the secreted cytokines from dendritic cells  and macrophages . Their collaboration with dendritic cells and macrophages provides the circulatory influence over the immune system. And the possible mediation of the suppressive effect of MSCs on B cells was studied that a CCL2 variant modified with matrix metalloproteinase has suppressed immunoglobulin production by plasma cells .
Recently, the dynamic expression of cytokines secreted from MSCs was reported to control T cell function and maturation by regulating the expression of FoxP3, prominently in T cell differentiation. Treg cells co-cultured with PMSCs significantly expanded in comparison with others with bone marrow-derived mesenchymal stem cells (BMSCs) . On the other hand, BMSCs should be harvested by an invasive procedure, are uncommon in the adult human bone marrow , and their number consequently reduces with the age of the person . But the placenta could be an abundant source of stem cells, no invasive procedures are required to gain the organ, and they are free from the ethical debate about their use as a source. The other advantages are that PMSCs have abilities of multi-lineage differentiation like BMSCs in the perspectives of morphology, cell surface antigen existence, and gene expression features; are capable of differentiation into various cell types; are easy to separate; and an abundant amount of MSCs can be taken in culture .
There are other molecules mediating the immunomodulatory events of MSCs such as IL-10, human leukocyte antigen G (HLA-G) [52,53,54], and leukemia inhibitory factor (LIF) , the latter of which plays a critical role in the regulation of T cell proliferation and production and preservation of Treg cells . Cultured placenta-derived MSCs produced the immunomodulatory effects in vivo, although in most cases, describing the molecules accountable for the discovered immunomodulation was disturbed by the complex communication between MSCs and endogenous cells, which stimulated the host’s intrinsic immune system. Regarding the immune tolerance of the eye, Wang et al. performed the experiment of the intact amniotic epithelium grafts from allogeneic GFP+ mice with syngeneic (EGFP-C57BL/6 to C57BL/6 W/t) and allogeneic (EGFP-C57BL/6 to BALB/c W/t). The major histocompatibility (MHC) class II+ antigens were quite less expressed post-implantation, when amniotic epithelial cells were implanted on the anterior surface of the eye or inserted into the anterior chambers of the eye. . Le Blanc et al. proposed that MSC infusions would be useful to treat severe patients with steroid refractory graft versus host disease .
In conclusion, although analyses of various orbital pathologies have been reported, studies on the therapeutic effects of stem cells have been lacking. This is the first report on the therapeutic effects of stem cells on a GO animal model. Based on our findings, we suggest that hPMSCs have immunomodulatory effects, inhibiting adipogenesis via anti-inflammatory effects. These results suggest that hPMSCs could potentially be used as a new therapy for GO disease.
Availability of data and materials
All data and materials are available upon request.
Human placenta-derived mesenchymal stem cells
Weetman AP. Graves’ disease. N Engl J Med. 2000;343(17):1236–48.
Bahn RS, Dutton CM, Natt N, Joba W, Spitzweg C, Heufelder AE. Thyrotropin receptor expression in Graves’ orbital adipose/connective tissues: potential autoantigen in Graves’ ophthalmopathy. J Clin Endocrinol Metab. 1998;83(3):998–1002.
Wiersinga WM, Smit T, van der Gaag R, Koornneef L. Temporal relationship between onset of Graves’ ophthalmopathy and onset of thyroidal Graves’ disease. J Endocrinol Investig. 1988;11(8):615–9.
Li YJ, Luo Y, Xie XQ, He WM, Yi C, Li P, et al. The efficacy of intensity modulated radiation therapy in treating thyroid-associated ophthalmopathy and predictive factors for treatment response. Sci Rep. 2017;7(1):17533.
Bartalena L, Pinchera A, Marcocci C. Management of Graves’ ophthalmopathy: reality and perspectives. Endocr Rev. 2000;21(2):168–99.
Burch HB, Wartofsky L. Graves’ ophthalmopathy: current concepts regarding pathogenesis and management. Endocr Rev. 1993;14(6):747–93.
Matthiesen C, Thompson JS, Thompson D, Farris B, Wilkes B, Ahmad S, et al. The efficacy of radiation therapy in the treatment of Graves’ orbitopathy. Int J Radiat Oncol Biol Phys. 2012;82(1):117–23.
Marquez SD, Lum BL, McDougall IR, Katkuri S, Levin PS, MacManus M, et al. Long-term results of irradiation for patients with progressive Graves’ ophthalmopathy. Int J Radiat Oncol Biol Phys. 2001;51(3):766–74.
Kotwal A, Stan M. Current and future treatments for Graves’ disease and Graves’ ophthalmopathy. Horm Metab Res. 2018;50(12):871–86.
Smith TJ. Challenges in orphan drug development: identification of effective therapy for thyroid-associated pphthalmopathy. Annu Rev Pharmacol Toxicol. 2019;59:129–48.
Meirelles Lda S, Fontes AM, Covas DT, Caplan AI. Mechanisms involved in the therapeutic properties of mesenchymal stem cells. Cytokine Growth Factor Rev. 2009;20(5–6):419–27.
Koch JM, D’Souza SS, Schwahn DJ, Dixon I, Hacker TA. Mesenchymoangioblast-derived mesenchymal stromal cells inhibit cell damage, tissue damage and improve peripheral blood flow following hindlimb ischemic injury in mice. Cytotherapy. 2016;18(2):219–28.
Park HW, Moon HE, Kim HS, Paek SL, Kim Y, Chang JW, et al. Human umbilical cord blood-derived mesenchymal stem cells improve functional recovery through thrombospondin1, pantraxin3, and vascular endothelial growth factor in the ischemic rat brain. J Neurosci Res. 2015;93(12):1814–25.
Huang W, Lv B, Zeng H, Shi D, Liu Y, Chen F, et al. Paracrine factors secreted by MSCs promote astrocyte survival associated with GFAP downregulation after ischemic stroke via p38 MAPK and JNK. J Cell Physiol. 2015;230(10):2461–75.
Bouchard CS, John T. Amniotic membrane transplantation in the management of severe ocular surface disease: indications and outcomes. Ocul Surf. 2004;2(3):201–11.
Ahmad S, Kolli S, Lako M, Figueiredo F, Daniels JT. Stem cell therapies for ocular surface disease. Drug Discov Today. 2010;15(7–8):306–13.
Mayer L, Pandak WM, Melmed GY, Hanauer SB, Johnson K, Payne D, et al. Safety and tolerability of human placenta-derived cells (PDA001) in treatment-resistant Crohn’s disease: a phase 1 study. Inflamm Bowel Dis. 2013;19(4):754–60.
Lublin FD, Bowen JD, Huddlestone J, Kremenchutzky M, Carpenter A, Corboy JR, et al. Human placenta-derived cells (PDA-001) for the treatment of adults with multiple sclerosis: a randomized, placebo-controlled, multiple-dose study. Mult Scler Relat Disord. 2014;3(6):696–704.
Baughman RP, Culver DA, Jankovi V, Fischkoff S, Brockway G, Lower EE. Placenta-derived mesenchymal like cells (PDA-001) as therapy for chronic pulmonary sarcoidosis: a phase 1 study. Sarcoidosis Vasc Diffuse Lung Dis. 2015;32(2):106–14.
Moshkelgosha S, So PW, Deasy N, Diaz-Cano S, Banga JP. Cutting edge: retrobulbar inflammation, adipogenesis, and acute orbital congestion in a preclinical female mouse model of Graves’ orbitopathy induced by thyrotropin receptor plasmid-in vivo electroporation. Endocrinology. 2013;154(9):3008–15.
Berchner-Pfannschmidt U, Moshkelgosha S, Diaz-Cano S, Edelmann B, Gortz GE, Horstmann M, et al. Comparative assessment of female mouse model of Graves’ orbitopathy under different environments, accompanied by proinflammatory cytokine and T-cell responses to thyrotropin hormone receptor antigen. Endocrinology. 2016;157(4):1673–82.
Lee HJ, Cha KE, Hwang SG, Kim JK, Kim GJ. In vitro screening system for hepatotoxicity: comparison of bone-marrow-derived mesenchymal stem cells and placenta-derived stem cells. J Cell Biochem. 2011;112(1):49–58.
Smith TJ. Is IGF-I receptor a target for autoantibody generation in Graves’ disease? J Clin Endocrinol Metab. 2013;98(2):515–8.
Morshed SA, Davies TF. Graves’ disease mechanisms: the role of stimulating, blocking, and cleavage region TSH receptor antibodies. Horm Metab Res. 2015;47(10):727–34.
Bahn RS, Heufelder AE. Pathogenesis of Graves’ ophthalmopathy. N Engl J Med. 1993;329(20):1468–75.
Nakahara M, Johnson K, Eckstein A, Taguchi R, Yamada M, Abiru N, et al. Adoptive transfer of antithyrotropin receptor (TSHR) autoimmunity from TSHR knockout mice to athymic nude mice. Endocrinology. 2012;153(4):2034–42.
Gilbert JA, Gianoukakis AG, Salehi S, Moorhead J, Rao PV, Khan MZ, et al. Monoclonal pathogenic antibodies to the thyroid-stimulating hormone receptor in Graves’ disease with potent thyroid-stimulating activity but differential blocking activity activate multiple signaling pathways. J Immunol. 2006;176(8):5084–92.
Kozdon K, Fitchett C, Rose GE, Ezra DG, Bailly M. Mesenchymal stem cell-like properties of orbital fibroblasts in Graves’ orbitopathy. Invest Ophthalmol Vis Sci. 2015;56(10):5743–50.
Brandau S, Bruderek K, Hestermann K, Gortz GE, Horstmann M, Mattheis S, et al. Orbital fibroblasts from Graves’ orbitopathy patients share functional and immunophenotypic properties with mesenchymal stem/stromal cells. Invest Ophthalmol Vis Sci. 2015;56(11):6549–57.
Nepali S, Park M, Lew H, Kim O. Comparative analysis of human adipose-derived mesenchymal stem cells from orbital and abdominal fat. Stem Cells Int. 2018;2018:3932615.
Muller-Forell W, Kahaly GJ. Neuroimaging of Graves’ orbitopathy. Best Pract Res Clin Endocrinol Metab. 2012;26(3):259–71.
San Miguel I, Arenas M, Carmona R, Rutllan J, Medina-Rivero F, Lara P. Review of the treatment of Graves’ ophthalmopathy: the role of the new radiation techniques. Saudi J Ophthalmol. 2018;32(2):139–45.
Arenas M, Gil F, Gironella M, Hernandez V, Jorcano S, Biete A, et al. Anti-inflammatory effects of low-dose radiotherapy in an experimental model of systemic inflammation in mice. Int J Radiat Oncol Biol Phys. 2006;66(2):560–7.
Arenas M, Sabater S, Jimenez PL, Rovirosa A, Biete A, Linares V, et al. Radiotherapy for Graves’ disease. The possible role of low-dose radiotherapy. Rep Pract Oncol Radiother. 2016;21(3):213–8.
Sanders J, Jeffreys J, Depraetere H, Evans M, Richards T, Kiddie A, et al. Characteristics of a human monoclonal autoantibody to the thyrotropin receptor: sequence structure and function. Thyroid. 2004;14(8):560–70.
Park M, Kim HC, Kim O, Lew H. Human placenta mesenchymal stem cells promote axon survival following optic nerve compression through activation of NF-kappaB pathway. J Tissue Eng Regen Med. 2018;12(3):e1441–e49.
Di Nicola M, Carlo-Stella C, Magni M, Milanesi M, Longoni PD, Matteucci P, et al. Human bone marrow stromal cells suppress T-lymphocyte proliferation induced by cellular or nonspecific mitogenic stimuli. Blood. 2002;99(10):3838–43.
Krampera M, Glennie S, Dyson J, Scott D, Laylor R, Simpson E, et al. Bone marrow mesenchymal stem cells inhibit the response of naive and memory antigen-specific T cells to their cognate peptide. Blood. 2003;101(9):3722–9.
Martinet L, Fleury-Cappellesso S, Gadelorge M, Dietrich G, Bourin P, Fournie JJ, et al. A regulatory cross-talk between Vgamma9Vdelta2 T lymphocytes and mesenchymal stem cells. Eur J Immunol. 2009;39(3):752–62.
Rasmusson I, Uhlin M, Le Blanc K, Levitsky V. Mesenchymal stem cells fail to trigger effector functions of cytotoxic T lymphocytes. J Leukoc Biol. 2007;82(4):887–93.
Corcione A, Benvenuto F, Ferretti E, Giunti D, Cappiello V, Cazzanti F, et al. Human mesenchymal stem cells modulate B-cell functions. Blood. 2006;107(1):367–72.
Traggiai E, Volpi S, Schena F, Gattorno M, Ferlito F, Moretta L, et al. Bone marrow-derived mesenchymal stem cells induce both polyclonal expansion and differentiation of B cells isolated from healthy donors and systemic lupus erythematosus patients. Stem Cells. 2008;26(2):562–9.
Sotiropoulou PA, Perez SA, Gritzapis AD, Baxevanis CN, Papamichail M. Interactions between human mesenchymal stem cells and natural killer cells. Stem Cells. 2006;24(1):74–85.
Spaggiari GM, Capobianco A, Becchetti S, Mingari MC, Moretta L. Mesenchymal stem cell-natural killer cell interactions: evidence that activated NK cells are capable of killing MSCs, whereas MSCs can inhibit IL-2-induced NK-cell proliferation. Blood. 2006;107(4):1484–90.
Aggarwal S, Pittenger MF. Human mesenchymal stem cells modulate allogeneic immune cell responses. Blood. 2005;105(4):1815–22.
Nemeth K, Leelahavanichkul A, Yuen PS, Mayer B, Parmelee A, Doi K, et al. Bone marrow stromal cells attenuate sepsis via prostaglandin E(2)-dependent reprogramming of host macrophages to increase their interleukin-10 production. Nat Med. 2009;15(1):42–9.
Rafei M, Hsieh J, Fortier S, Li M, Yuan S, Birman E, et al. Mesenchymal stromal cell-derived CCL2 suppresses plasma cell immunoglobulin production via STAT3 inactivation and PAX5 induction. Blood. 2008;112(13):4991–8.
Kim SH, Jung J, Cho KJ, Choi JH, Lee HS, Kim GJ, et al. Immunomodulatory effects of placenta-derived mesenchymal stem cells on T cells by regulation of FoxP3 expression. Int J Stem Cells. 2018;11(2):196–204.
Pittenger MF, Mackay AM, Beck SC, Jaiswal RK, Douglas R, Mosca JD, et al. Multilineage potential of adult human mesenchymal stem cells. Science. 1999;284(5411):143–7.
Rao MS, Mattson MP. Stem cells and aging: expanding the possibilities. Mech Ageing Dev. 2001;122(7):713–34.
Shehadah A, Chen J, Pal A, He S, Zeitlin A, Cui X, et al. Human placenta-derived adherent cell treatment of experimental stroke promotes functional recovery after stroke in young adult and older rats. PLoS One. 2014;9(1):e86621.
Nasef A, Chapel A, Mazurier C, Bouchet S, Lopez M, Mathieu N, et al. Identification of IL-10 and TGF-beta transcripts involved in the inhibition of T-lymphocyte proliferation during cell contact with human mesenchymal stem cells. Gene Expr. 2007;13(4–5):217–26.
Nasef A, Mathieu N, Chapel A, Frick J, Francois S, Mazurier C, et al. Immunosuppressive effects of mesenchymal stem cells: involvement of HLA-G. Transplantation. 2007;84(2):231–7.
Rizzo R, Campioni D, Stignani M, Melchiorri L, Bagnara GP, Bonsi L, et al. A functional role for soluble HLA-G antigens in immune modulation mediated by mesenchymal stromal cells. Cytotherapy. 2008;10(4):364–75.
Nasef A, Mazurier C, Bouchet S, Francois S, Chapel A, Thierry D, et al. Leukemia inhibitory factor: role in human mesenchymal stem cells mediated immunosuppression. Cell Immunol. 2008;253(1–2):16–22.
Di Ianni M, Del Papa B, De Ioanni M, Moretti L, Bonifacio E, Cecchini D, et al. Mesenchymal cells recruit and regulate T regulatory cells. Exp Hematol. 2008;36(3):309–18.
Wang M, Yoshida A, Kawashima H, Ishizaki M, Takahashi H, Hori J. Immunogenicity and antigenicity of allogeneic amniotic epithelial transplants grafted to the cornea, conjunctiva, and anterior chamber. Invest Ophthalmol Vis Sci. 2006;47(4):1522–32.
Le Blanc K, Rasmusson I, Sundberg B, Gotherstrom C, Hassan M, Uzunel M, et al. Treatment of severe acute graft-versus-host disease with third party haploidentical mesenchymal stem cells. Lancet. 2004;363(9419):1439–41.
This research was supported by the Ministry of Health & Welfare, Republic of Korea (Grant/Award No. HI16C1559).
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The process of obtaining orbital adipose tissue was approved by the Institutional Review Board of Bundang CHA Medical Center (Seongnam-si, South Korea), and the animal protocol was approved by the Institutional Animal Care and Use Committee of CHA Bundang Medical Center.
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Park, M., Banga, J.P., Kim, G.J. et al. Human placenta-derived mesenchymal stem cells ameliorate orbital adipogenesis in female mice models of Graves’ ophthalmopathy. Stem Cell Res Ther 10, 246 (2019). https://doi.org/10.1186/s13287-019-1348-0
- Graves’ ophthalmopathy
- Graves’ disease
- GO animal model
- Thyroid disease