Exosomes From Adipose-Derived Stem Cells Suppress the Progression of Chronic Endometritis

微泡 间质细胞 炎症 癌症研究 肿瘤坏死因子α 脂肪组织 子宫内膜炎 细胞凋亡 外体 干细胞 TLR4型 细胞因子 医学 细胞生物学 免疫学 生物 内科学 小RNA 基因 生物化学 遗传学 怀孕
作者
Bin Wang,Li Li,R Xiao yu
出处
期刊:Cell Transplantation [SAGE Publishing]
卷期号:32: 9636897231173736-9636897231173736 被引量:14
标识
DOI:10.1177/09636897231173736
摘要

Chronic endometritis (CE) is closely linked to the reproductive failure. Exosome (Exo)-based therapy is proposed as an encouraging strategy in inflammation-related disorders; however, little work has been devoted to its usage in CE therapy. An in vitro CE was established by administration of lipopolysaccharide (LPS) in human endometrial stromal cells (HESCs). The cell proliferation, cell apoptosis, and inflammatory cytokine assays were performed in vitro, and the efficacy of Exos derived from adipose tissue-derived stem cells (ADSCs) was evaluated in a mouse model of CE. We found that Exos isolated from ADSCs could be taken up by HESCs. Exos elevated the proliferation and inhibited apoptosis in LPS-treated HESCs. Administration of Exos to HESCs suppressed the content of tumor necrosis factor-alpha (TNF-α), interleukin-6 (IL-6), and interleukin-1β (IL-1β). Moreover, Exos exposure repressed the inflammation stimulated by LPS in vivo. Mechanistically, we demonstrated that Exos exerted their ant-inflammatory effect via miR-21/TLR4/NF-kB signaling pathway in endometrial cells. Our findings suggest that ADSC-Exo-based therapy might serve as an attractive strategy for the treatment of CE.
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