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

Author:

Sun Huijun1ORCID,Dong Jie1,Fu Zhaoyue2,Lu Xueyan1,Chen Xutao2,Lei Hui1,Xiao Xifeng1,Chen Shuqiang1,Lu Jie1,Su Danjie1,Xiong Yujing12,Fang Zheng1,Mao Jiaqin1,Chen Lihua2,Wang Xiaohong1ORCID

Affiliation:

1. Reproductive Medicine Center Department of Gynecology and Obstetrics Tangdu Hospital Clinical Research Center for Reproductive Medicine and Gynecological Endocrine Diseases of Shaanxi Province Air Force Medical University No.1 Xinsi Road Xi'an 710038 China

2. Department of Immunology School of Basic Medicine Air Force Medical University No.169 West Changle Road Xi'an 710038 China

Abstract

AbstractIntrauterine 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.

Funder

National Natural Science Foundation of China

Publisher

Wiley

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