微泡
自噬
间充质干细胞
细胞生物学
炎症
椎间盘
外体
癌症研究
生物
免疫学
小RNA
细胞凋亡
解剖
生物化学
基因
作者
Baicheng Yang,Xinming Yang
出处
期刊:Folia Morphologica
[VM Media Sp zo.o. - VMGroup SK]
日期:2023-03-27
卷期号:83 (1): 102-112
被引量:6
标识
DOI:10.5603/fm.a2023.0021
摘要
Intervertebral disc degenerative diseases (IDDD) is one the main causes of lumbago, and its main pathological mechanism is intervertebral disc degeneration (IDD). In previous reports, mesenchymal stem cell (MSC)-exosomes can slow down or even reverse degenerated nucleus pulposus (NP) cells in IDD. Thus, we attempted to clarify specific role of MSC-exosomes underlying IDD progression. In the present study, the harvested particles were identified as MSC-exosomes. MSC-exosomes facilitated activation of autophagy pathway in AGE-treated NP cells. MSC-exosomes repressed inflammatory response in AGE-treated NP cells. Autophagy pathway activation enhanced inflammatory response in AGE-stimulated NP cells. MSC-exosomes facilitated autophagy pathway activation and repressed inflammation in IDD rats. Autophagy inhibition exerted a protective role against inflammatory response in IDD rats. In conclusion, MSC-exosomes represses inflammation via activating autophagy pathway, which provides a potential novel insight for seeking therapeutic plans of IDD.
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