Regulation of the Th17/Treg balance by human umbilical cord mesenchymal stem cell-derived exosomes protects against acute experimental colitis

间充质干细胞 结肠炎 外体 微泡 免疫系统 生物 免疫学 炎症 脾脏 细胞生物学 小RNA 生物化学 基因
作者
Neda Heidari,Hajar Abbasi-Kenarsari,Saeed Namaki,Kaveh Baghaei,Mohammad Reza Zali,Zahra Mirsanei,Seyed Mahmoud Hashemi
出处
期刊:Experimental Cell Research [Elsevier]
卷期号:419 (1): 113296-113296 被引量:6
标识
DOI:10.1016/j.yexcr.2022.113296
摘要

Increasing evidence suggests that mesenchymal stem cells (MSCs) have immunosuppressive properties mediated by MSC-derived small extracellular vesicles (sEV). Exosomes are small extracellular vesicles that contain components that regulate immune cell function. We investigated the immunomodulatory effects of MSC-derived Exosome (MSC-Exo) on the severity of colitis using the dextran sulfate sodium (DSS)-induced colitis model. Exosomes were administrated intraperitoneally. Daily changes in body weight, stool consistency, and bleeding were assessed to determine the impact of MSC-Exos on colitis. Several measurements were taken, including the colon weight, length, and histological analysis of the colon tissues. The percentage of regulatory T cells and IL-10, TGF-β, IL-17, TNF-α, and IFN-γ levels were calculated in the mesenteric lymph node (MLN) and spleen. The results showed MSC-Exos improved clinical manifestations of colitis. Colon macroscopic and histological observations also showed improvement in tissue destruction. The results illustrated that MSC-Exos might attenuate colitis by regulating Treg/Th17 balance, increasing anti-inflammatory, and decreasing pro-inflammatory cytokines expression. As a result, MSC-Exos could be used as an immunomodulatory approach to treating bowel inflammation.
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