粒体自噬
帕金
细胞生物学
间充质干细胞
基因敲除
干细胞
肿瘤坏死因子α
线粒体
骨髓
衰老
化学
生物
自噬
免疫学
细胞凋亡
医学
病理
生物化学
帕金森病
疾病
作者
Fan Pan,Xiaoyu Yu,Changhong Chen,Jiawei Gao,Yuzhu Xu,Xinhui Xie,Yuntao Wang
标识
DOI:10.1016/j.exger.2022.111829
摘要
Bone marrow mesenchymal stem cells (BMSCs) have been investigated as cellular therapeutics for intervertebral disc degeneration. However, transplanted BMSCs are prone to be damaged. TNF-α is reported to extensively promote degeneration process. Nevertheless, the relationship between BMSCs senescence and TNF-α-induced stress has not been elucidated. Previous studies showed that mitophagy is a crucial factor in maintaining cellular homeostasis. Hence, we sought to clarify the role and mechanism of mitophagy in TNF-α-induced biological changes of BMSCs. Here, we found that TNF-α caused transient senescent damage in the early stage. Meanwhile, Parkin-mediated mitophagy was initiated and weakened the damage through maintaining mitochondria homeostasis. After inhibiting mitophagy by knockdown of Parkin, TNF-α irreversibly caused cellular senescence. These results suggested that Parkin-mediated mitophagy played protective role in BMSCs in response to TNF-α, which could be a crucial therapeutic target in the future.
科研通智能强力驱动
Strongly Powered by AbleSci AI