TSG6‐Exo@CS/GP Attenuates Endometrium Fibrosis by Inhibiting Macrophage Activation in a Murine IUA Model

巨噬细胞 间质细胞 纤维化 炎症 子宫内膜 微泡 M2巨噬细胞 肿瘤坏死因子α 癌症研究 男科 内科学 化学 生物化学 医学 小RNA 体外 基因
作者
H. Sun,Jie Dong,Zhaoyue Fu,Xueyan Lu,Xutao Chen,Hui Lei,Xifeng Xiao,Shuqiang Chen,Jie Lu,Danjie Su,Yujing Xiong,Zheng Fang,Jiaqin Mao,Lihua Chen,Xiaohong Wang
出处
期刊:Advanced Materials [Wiley]
卷期号:36 (21) 被引量:8
标识
DOI:10.1002/adma.202308921
摘要

Intrauterine adhesion (IUA) is characterized by the formation of fibrous scar tissue within the uterine cavity, which significantly impacts female reproductive health and even leads to infertility. Unfortunately, severe cases of IUA currently lack effective treatments. This study presents a novel approach that utilizes tumor necrosis factor-(TNF) stimulated gene 6 (TSG6)-modified exosomes (Exos) in conjunction with an injectable thermosensitive hydrogel (CS/GP) to mitigate the occurrence of IUA by reducing endometrium fibrosis in a mouse IUA model. This study demonstrate that TSG6-modified Exos effectively inhibits the activation of inflammatory M1-like macrophages during the initial stages of inflammation and maintains the balance of macrophage phenotypes (M1/M2) during the repair phase. Moreover, TSG6 inhibits the interaction between macrophages and endometrial stromal fibroblasts, thereby preventing the activation of stromal fibroblasts into myofibroblasts. Furthermore, this research indicates that CS/GP facilitates the sustained release of TSG6-modified Exos, leading to a significant reduction in both the manifestations of IUA and the extent of endometrium fibrosis. Collectively, through the successful construction of CS/GP loaded with TSG6-modified Exos, a reduction in the occurrence and progression of IUA is achieved by mitigating endometrium fibrosis. Consequently, this approach holds promise for the treatment of IUA.
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