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:31
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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