再生(生物学)
间质细胞
间充质干细胞
微泡
血管生成
细胞生物学
子宫内膜
不育
化学
男科
医学
生物
癌症研究
怀孕
内科学
生物化学
小RNA
遗传学
基因
作者
Yuxiang Liang,Qizhi Shuai,Xiao Zhang,Shanshan Jin,Yuqian Guo,Zhaowei Yu,Xinrui Xu,Ruifang Ao,Zhiwei Peng,Huimin Lv,Sheng He,Chunfang Wang,Guohua Song,Zhizhen Liu,Hong Zhao,Qilong Feng,Ruochen Du,Bin Zheng,Zhaoyang Chen,Jun Xie
标识
DOI:10.1002/adhm.202303674
摘要
Abstract Intrauterine adhesion (IUA) stands as a prevalent medical condition characterized by endometrial fibrosis and scar tissue formation within the uterine cavity, resulting in infertility and, in severe cases, recurrent miscarriages. Cell therapy, especially with stem cells, offers an alternative to surgery, but concerns about uncontrolled differentiation and tumorigenicity limit its use. Exosomes, more stable and immunogenicity‐reduced than parent cells, have emerged as a promising avenue for IUA treatment. In this study, a novel approach has been proposed wherein exosomes originating from decidual stromal cells (DSCs) are encapsulated within sodium alginate hydrogel (SAH) scaffolds to repair endometrial damage and restore fertility in a mouse IUA model. Current results demonstrate that in situ injection of DSC‐derived exosomes (DSC‐exos)/SAH into the uterine cavity has the capability to induce uterine angiogenesis, initiate mesenchymal‐to‐epithelial transformation (MET), facilitate collagen fiber remodeling and dissolution, promote endometrial regeneration, enhance endometrial receptivity, and contribute to the recovery of fertility. RNA sequencing and advanced bioinformatics analysis reveal miRNA enrichment in exosomes, potentially supporting endometrial repair. This finding elucidates how DSC‐exos/SAH mechanistically fosters collagen ablation, endometrium regeneration, and fertility recovery, holding the potential to introduce a novel IUA treatment and offering invaluable insights into the realm of regenerative medicine.
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