Autophagic LC3 + calcified extracellular vesicles initiate cartilage calcification in osteoarthritis

Author:

Yan Jianfei1ORCID,Shen Minjuan1ORCID,Sui Bingdong2ORCID,Lu Weicheng1ORCID,Han Xiaoxiao1ORCID,Wan Qianqian1ORCID,Liu Yingying3ORCID,Kang Junjun3ORCID,Qin Wenpin1ORCID,Zhang Zibing1ORCID,Chen Da2ORCID,Cao Yuan2ORCID,Ying Siqi2ORCID,Tay Franklin R.4ORCID,Niu Li-na1ORCID,Jiao Kai1ORCID

Affiliation:

1. State Key Laboratory of Military Stomatology and National Clinical Research Center for Oral Diseases and Shaanxi Key Laboratory of Stomatology, School of Stomatology, The Fourth Military Medical University, Xi’an, Shaanxi, China.

2. State Key Laboratory of Military Stomatology and National Clinical Research Center for Oral Diseases and Shaanxi International Joint Research Center for Oral Diseases, Center for Tissue Engineering, School of Stomatology, The Fourth Military Medical University, Xi’an, Shaanxi, China.

3. Department of Neurobiology, The Fourth Military Medical University, Xi’an, Shaanxi, China.

4. The Graduate School, Augusta University, Augusta, GA, USA.

Abstract

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.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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