血管生成
间充质干细胞
微泡
心肌梗塞
骨髓
医学
干细胞
细胞凋亡
癌症研究
免疫学
细胞生物学
病理
生物
内科学
生物化学
小RNA
基因
作者
Zhongxin Sha,Wupeng Liu,Tianpeng Jiang,Kaiping Zhang,Zhenqiu Yu
标识
DOI:10.1080/02648725.2023.2194087
摘要
Bone marrow mesenchymal stem cells (BMECs)-derived exosomes (MSC-Exo) can improve acute myocardial infarction (AMI). Astragaloside IV (AS-IV) has also been reported to have cardioprotective pharmacological effects. However, it is not entirely clear whether AS-IV can improve AMI by inducing MSC-Exo. BMSCs and MSC-Exo were isolated and identified, and we also established the AMI rat model and the OGD/R model with H9c2 cells. After MSC-Exo or AS-IV-mediated MSC-Exo treatment, cell angiogenesis, migration, and apoptosis were evaluated by tube formation, wound healing, and TUNEL staining. The cardiac function of the rats was measured by echocardiography. The pathological changes and collagen deposition in rats were also assessed with Masson and Sirius red staining. The levels of α-SMA, CD31 and inflammatory factors were determined by immunohistochemistry and enzyme-linked immunosorbent assay (ELISA).
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