Xenogeneic Sertoli cells modulate immune response in an evolutionary distant mouse model through the production of interleukin-10 and PD-1 ligands expression
Jazyk angličtina Země Dánsko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
35297099
DOI
10.1111/xen.12742
Knihovny.cz E-zdroje
- Klíčová slova
- Sertoli cells, immunomodulation, xenotransplantation,
- MeSH
- antigeny CD274 MeSH
- antigeny CD279 * MeSH
- imunita MeSH
- interleukin-10 * MeSH
- ligandy MeSH
- modely nemocí na zvířatech MeSH
- myši MeSH
- Sertoliho buňky MeSH
- transplantace heterologní MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- antigeny CD274 MeSH
- antigeny CD279 * MeSH
- interleukin-10 * MeSH
- ligandy MeSH
BACKGROUND: Immunomodulatory mechanisms of Sertoli cells (SCs) during phylogeny have not been described previously. This study attempted to reveal mechanisms of SC immune modulation in an evolutionary distant host. METHODS: The interaction of the SC cell line derived from Xenopus tropicalis (XtSC) with murine immune cells was studied in vivo and in vitro. The changes in the cytokine production, the intracellular and surface molecules expression on murine immune cells were evaluated after co-culturing with XtSCs. Migration of XtSCs in mouse recipients after intravenous application and subsequent changes in spleen and the testicular immune environment were determined by flow cytometry. RESULTS: The in vitro co-culture model was established, allowing the study of XtSCs interaction with murine immune cells. Intracellular staining of interleukin (IL-)10 revealed a significant increase in its expression in macrophages and B cells co-cultured with XtSCs, compared to both unstimulated cells and xenogeneic control. On the contrary, a significant decrease in Th lymphocytes expressing interferon-gamma was observed. The expression of both PD-1 ligands (PD-L1 and PD-L2) was upregulated on the macrophage surfaces after co-culture with XtSCs, but not with the controls. XtSCs migrated specifically to testes when administered intravenously and modulated systemic and local testicular microenvironment; this was detected by the expression of molecules associated with suppressive phenotype by CD45+ cells in both spleen and testes. CONCLUSION: We have demonstrated for the first time that SCs can migrate and modulate immune response in a phylogenetically distant host. It was further observed that SCs induce expression of molecules associated with immunosuppression, such as IL-10 and PD-1 ligands.
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Dufour JM, Hamilton M, Rajotte RV, Korbutt GS. Neonatal porcine Sertoli cells inhibit human natural antibody-mediated lysis. Biol Reprod. 2005;72:1224-1231.
Dufour JM, Rajotte RV, Kin T, Korbutt GS. Immunoprotection of rat islet xenografts by cotransplantation with sertoli cells and a single injection of antilymphocyte serum. Transplantation. 2003;75:1594-1596.
Dal Secco V, Riccioli A, Padula F, Ziparo E, Filippini A. Mouse Sertoli cells display phenotypical and functional traits of antigen-presenting cells in response to interferon gamma. Biol Reprod. 2008;78:234-242.
Wright K, Dziuk R, Mital P, Kaur G, Dufour JM. Xenotransplanted pig Sertoli cells inhibit both the alternative and classical pathways of complement-mediated cell lysis while pig islets are killed. Cell Transplant. 2016;25:2027-2040.
Campese AF, Grazioli P, de Cesaris P, et al. Mouse Sertoli cells sustain de novo generation of regulatory T cells by triggering the notch pathway through soluble JAGGED11. Biol Reprod. 2014;90:53-54.
Kaur G, Mital P, Dufour JM. Testisimmune privilege-assumptions versus facts. Anim Reprod. 2013;10:3-15.
Luca G, Arato I, Sorci G, et al. Sertoli cells for cell transplantation: pre-clinical studies and future perspectives. Andrology. 2018;6:385-395.
Takemoto N, Liu X, Takii K, Teramura Y, Iwata H. Transplantation of co-aggregates of Sertoli cells and islet cells into liver without immunosuppression. Transplantation. 2014;97:287-293.
Shamekh R, El-Badri NS, Saporta S, et al. Sertoli cells induce systemic donor-specific tolerance in xenogenic transplantation model. Cell Transplant. 2006;15:45-53.
Lim HG, Lee HM, Oh BC, Lee JR. Cell-mediated immunomodulation of chemokine receptor 7-expressing porcine Sertoli cells in murine heterotopic heart transplantation. J Hear Lung Transplant. 2009;28:72-78.
Mai HX, Yu L, Chen LJ, et al. Renoprotective effects of cotransplanted allogeneic testicular Sertoli cells in a renal acute rejection model in rats. Exp Clin Transplant. 2012;10:554-560.
Rahman TM, Diakanov I, Selden C, Hodgson H. Co-transplantation of encapsulated HepG2 and rat Sertoli cells improves outcome in a thioacetamide induced rat model of acute hepatic failure. Transpl Int. 2005;18:1001-1009.
Milanizadeh S, Zuwarali KNN, Aliaghaei A, Bigdeli MR. Therapeutic potential of pretreatment with allograft Sertoli cells transplantation in brain ischemia by improving oxidative defenses. J Mol Neurosci. 2018;64:533-542.
Dufour JM, Rajotte RV, Seeberger K, Kin T, Korbutt GS. Long-term survival of neonatal porcine Sertoli cells in non-immunosuppressed rats. Xenotransplantation. 2003;10:577-586.
Saporta S, Cameron DF, Borlongan CV, Sanberg PR. Survival of rat and porcine Sertoli cell transplants in the rat striatum without cyclosporine-A immunosuppression. Exp Neurol. 1997;146:299-304.
Mital P, Kaur G, Dufour JM. Immunoprotective Sertoli cells: making allogeneic and xenogeneic transplantation feasible. Reproduction. 2010;139:495-504.
Jhao YT, Chiu CH, Chen CFF, et al. The effect of Sertoli cells on xenotransplantation and allotransplantation of ventral mesencephalic tissue in a rat model of Parkinson's disease. Cells. 2019;8:1420.
Kaur G, Wright K, Mital P, et al. Neonatal pig Sertoli cells survive xenotransplantation by creating an immune modulatory environment involving CD4 and CD8 regulatory T cells. Cell Transplant. 2020;29:963689720947102.
Tlapakova T, Nguyen TMX, Vegrichtova M, et al. Identification and characterization of Xenopus tropicalis common progenitors of Sertoli and peritubular myoid cell lineages. Biol Open. 2016;5:1275-1282.
Nguyen TMX, Vegrichtova M, Tlapakova T, Krulova M, Krylov V. Epithelial-mesenchymal transition promotes the differentiation potential of xenopus tropicalis immature Sertoli cells. Stem Cells Int. 2019;2019:8387478.
Sinzelle L, Thuret R, Hwang HY, et al. Characterization of a novel Xenopus tropicalis cell line as a model for in vitro studies. Genesis. 2012;50:316-324.
Ostrand-Rosenberg S, Horn LA, Haile ST. The programmed Death-1 immune-suppressive pathway: barrier to antitumor immunity. J Immunol. 2014;193:3835-3841.
Plege-Fleck A, Lieke T, Römermann D, et al. Pig to rat cell transplantation: reduced cellular and antibody responses to xenografts overexpressing PD-L1. Xenotransplantation. 2014;21:533-542.
Ma D, Duan W, Li Y, et al. PD-L1 deficiency within islets reduces allograft survival in mice. PLoS One. 2016;11:e0152087.
Jin X, Wang Y, Hawthorne WJ, et al. Enhanced suppression of the xenogeneic T-cell response in vitro by xenoantigen stimulated and expanded regulatory T cells. Transplantation. 2014;97:30-38.
Sun L, Yi S, O'Connell PJ. IL-10 is required for human CD4(+)CD25(+) regulatory T cell-mediated suppression of xenogeneic proliferation. Immunol Cell Biol. 2010;88:477-485.
Kaur G, Thompson LA, Dufour JM. Sertoli cells-Immunological sentinels of spermatogenesis. Semin Cell Dev Biol. 2014;30:36-44.
Porubska B, Vasek D, Somova V, et al. Sertoli cells possess immunomodulatory properties and the ability of mitochondrial transfer similar to mesenchymal stromal cells. Stem Cell Rev Rep. 2021;17:1905-1916.
França LR, Hess RA, Dufour JM, Hofmann MC, Griswold MD. The Sertoli cell: one hundred fifty years of beauty and plasticity. Andrology. 2016;4:189-212.
Schulz RW, Nóbrega RH, Morais RDVS, et al. Endocrine and paracrine regulation of zebrafish spermatogenesis: the Sertoli cell perspective. Anim Reprod. 2015;12:81-87.
Lacerda SMdosSN, Costa GMJ, de França LR. Biology and identity of fish spermatogonial stem cell. Gen Comp Endocrinol. 2014;207:56-65.
Sohni A, Verfaillie CM. Mesenchymal stem cells migration homing and tracking. Stem Cells Int. 2013;2013:130763.
Doyle TJ, Kaur G, Putrevu SM, et al. Immunoprotective properties of primary Sertoli cells in mice: potential functional pathways that confer immune privilege. Biol Reprod. 2012;86:1-14.
Taube JM, Young GD, McMiller TL, et al. Differential expression of immune-regulatory genes associated with PD-L1 display in melanoma: implications for PD-1 pathway blockade. Clin Cancer Res. 2015;21:3969.
Samiea A, Yoon JSJ, Ong CJ, et al. Interleukin-10 Induces expression of neuroendocrine markers and PDL1 in prostate cancer cells. Prostate Cancer. 2020;2020:5305306.
de Witte SFH, Luk F, Parraga JMS, et al. Immunomodulation by therapeutic mesenchymal stromal cells (MSC) is triggered through phagocytosis of MSC by monocytic cells. Stem Cells. 2018;36:602-615.
Kaur G, Vadala S, Dufour JM. An overview of a Sertoli cell transplantation model to study testis morphogenesis and the role of the Sertoli cells in immune privilege. Environ Epigenet. 2017;3:dvx012.
Ezzelarab MB. Regulatory T cells from allo- to xenotransplantation: opportunities and challenges. Xenotransplantation. 2018;25:e12415.
Lee FT, Dangi A, Shah S, et al. Rejection of xenogeneic porcine islets in humanized mice is characterized by graft-infiltrating Th17 cells and activated B cells. Am J Transplant. 2020;20:1538-1550.
Liu Z, Fan H, Jiang S. CD4(+) T-cell subsets in transplantation. Immunol Rev. 2013;252:183-191.
Shilling RA, Wilkes DS. Role of Th17 cells and IL-17 in lung transplant rejection. Semin Immunopathol. 2011;33:129-134.
Rosborough BR, Raïch-Regué D, Turnquist HR, Thomson AW. Regulatory myeloid cells in transplantation. Transplantation. 2014;97:367-379.
Scalea JR, Tomita Y, Lindholm CR, Burlingham W. Transplantation tolerance induction: cell therapies and their mechanisms. Front Immunol. 2016;7:87.
Huber S, Hoffmann R, Muskens F, Voehringer D. Alternatively activated macrophages inhibit T-cell proliferation by Stat6-dependent expression of PD-L2. Blood. 2010;116:3311-3320.
Yang H, Wright JR. Co-encapsulation of Sertoli enriched testicular cell fractions further prolongs fish-to-mouse islet xenograft survival. Transplantation. 1999;67:815-820.
Wright JR Jr, Yang H, Hyrtsenko O, et al. A review of piscine islet xenotransplantation using wild-type tilapia donors and the production of transgenic tilapia expressing a “humanized” tilapia insulin. Xenotransplantation. 2014;21:485-495.
Yang H, Al-Jazaeri A. The immunoprotective effect of Sertoli cells coencapsulated with islet xenografts is not dependent upon Fas ligand expression. Cell Transplant. 2002;11:799-801.
Bistoni G, Calvitti M, Mancuso F, et al. Prolongation of skin allograft survival in rats by the transplantation of microencapsulated xenogeneic neonatal porcine Sertoli cells. Biomaterials. 2012;33:5333-5340.