自噬
钙化
骨关节炎
软骨
细胞生物学
HDAC6型
细胞外
化学
病态的
病理
生物
医学
癌症研究
组蛋白脱乙酰基酶
组蛋白
解剖
生物化学
细胞凋亡
基因
替代医学
作者
Jianfei Yan,Min‐juan Shen,Bing‐Dong Sui,Weicheng Lu,Xiaoxiao Han,Qian‐qian Wan,Yingying Liu,Jun‐Jun Kang,Wenpin Qin,Zibing Zhang,Da Chen,Yuan Cao,Si-Qi Ying,Franklin R. Tay,Li‐na Niu,Kai Jiao
出处
期刊:Science Advances
[American Association for the Advancement of Science (AAAS)]
日期:2022-05-13
卷期号:8 (19)
被引量:29
标识
DOI:10.1126/sciadv.abn1556
摘要
Pathological cartilage calcification plays an important role in osteoarthritis progression but in which the origin of calcified extracellular vesicles (EVs) and their effects remain unknown. Here, we demonstrate that pathological cartilage calcification occurs in the early stage of the osteoarthritis in which the calcified EVs are closely involved. Autophagosomes carrying the minerals are released in EVs, and calcification is induced by those autophagy-regulated calcified EVs. Autophagy-derived microtubule-associated proteins 1A/1B light chain 3B (LC3)-positive EVs are the major population of calcified EVs that initiate pathological calcification. Release of LC3-positive calcified EVs is caused by blockage of the autophagy flux resulted from histone deacetylase 6 (HDAC6)-mediated microtubule destabilization. Inhibition of HDAC6 activity blocks the release of the LC3-positive calcified EVs by chondrocytes and effectively reverses the pathological calcification and degradation of cartilage. The present work discovers that calcified EVs derived from autophagosomes initiate pathological cartilage calcification in osteoarthritis, with potential therapeutic targeting implication.
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