Effects of Mesenchymal Stem Cell-Derived Exosomes on Experimental Autoimmune Uveitis

We previously demonstrated that mesenchymal stem cells (MSCs) ameliorated experimental autoimmune uveoretinitis (EAU) in rats. Recently, MSC-derived exosomes (MSC-Exo) were thought to carry functions of MSCs. In this study, we tested the effect of local administration of human MSC-Exo on established...

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Published inScientific reports Vol. 7; no. 1; pp. 4323 - 11
Main Authors Bai, Lingling, Shao, Hui, Wang, Hongxing, Zhang, Zhihui, Su, Chang, Dong, Lijie, Yu, Bo, Chen, Xiteng, Li, Xiaorong, Zhang, Xiaomin
Format Journal Article
LanguageEnglish
Published England Nature Publishing Group 28.06.2017
Nature Publishing Group UK
Nature Portfolio
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Summary:We previously demonstrated that mesenchymal stem cells (MSCs) ameliorated experimental autoimmune uveoretinitis (EAU) in rats. Recently, MSC-derived exosomes (MSC-Exo) were thought to carry functions of MSCs. In this study, we tested the effect of local administration of human MSC-Exo on established EAU in the same species. Rats with EAU induced by immunization with interphotoreceptor retinol-binding protein 1177-1191 peptide were treated by periocular injections of increasing doses of MSC-Exo starting at the disease onset for 7 consecutive days. The in vitro effects of MSC-Exo on immune cell migration and responder T cell proliferation were examined by chemotactic assays and lymphocyte proliferation assays, respectively. We found that MSC-Exo greatly reduced the intensity of ongoing EAU as their parent cells by reducing the infiltration of T cell subsets, and other inflammatory cells, in the eyes. Furthermore, the chemoattractive effects of CCL2 and CCL21 on inflammatory cells were inhibited by MSC-Exo. However, no inhibitory effect of MSC-Exo on IRBP-specific T cell proliferation was observed. These results suggest that MSC-Exo effectively ameliorate EAU by inhibiting the migration of inflammatory cells, indicating a potential novel therapy of MSC-Exo for uveitis.
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ISSN:2045-2322
2045-2322
DOI:10.1038/s41598-017-04559-y