miR-199a-5p Reduces Chondrocyte Hypertrophy and Attenuates Osteoarthritis Progression via the Indian Hedgehog Signal Pathway

Author:

Huang Lei12,Jin Meng2,Gu Ruiying3,Xiao Kunlin12,Lu Mengnan3,Huo Xinyu3,Sun Mengyao3,Yang Zhi1,Wang Zhiyuan1,Zhang Weijie1,Zhi Liqiang1,Meng Ziang4,Ma Jie3,Ma Jianbing1,Zhang Rui2

Affiliation:

1. Department of Joint Surgery, Honghui Hospital, Xi’an Jiaotong University, Xi’an 710054, China

2. Translational Medicine Center, Honghui Hospital, Xi’an Jiaotong University, Xi’an 710054, China

3. School of Basic Medical Science, Xi’an Jiaotong University Health Science Center, Xi’an 710049, China

4. Department of Mathematics and Computing Science, Simon Fraser University, Vancouver, BC V6B 5K3, Canada

Abstract

Osteoarthritis (OA), the most common type of arthritis, is an age-associated disease, characterized by the progressive degradation of articular cartilage, synovial inflammation, and degeneration of subchondral bone. Chondrocyte proliferation is regulated by the Indian hedgehog (IHH in humans, Ihh in animals) signaling molecule, which regulates hypertrophy and endochondral ossification in the development of the skeletal system. microRNAs (miRNAs, miRs) are a family of about 22-nucleotide endogenous non-coding RNAs, which negatively regulate gene expression. In this study, the expression level of IHH was upregulated in the damaged articular cartilage tissues among OA patients and OA cell cultures, while that of miR-199a-5p was the opposite. Further investigations demonstrated that miR-199a-5p could directly regulate IHH expression and reduce chondrocyte hypertrophy and matrix degradation via the IHH signal pathway in the primary human chondrocytes. The intra-articular injection of synthetic miR-199a-5p agomir attenuated OA symptoms in rats, including the alleviation of articular cartilage destruction, subchondral bone degradation, and synovial inflammation. The miR-199a-5p agomir could also inhibit the Ihh signaling pathway in vivo. This study might help in understanding the role of miR-199a-5p in the pathophysiology and molecular mechanisms of OA and indicate a potential novel therapeutic strategy for OA patients.

Funder

Natural Science Foundation of Shaanxi Province

Key Science and Technology Program of Shaanxi Province

Science Foundation of Xi’an Municipal Health Commission

National Natural Science Foundation of China

Publisher

MDPI AG

Subject

General Medicine

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