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miR-199a-5p通过印度刺猬信号通路减少软骨细胞肥大并减缓骨关节炎进展。

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

作者信息

Huang Lei, Jin Meng, Gu Ruiying, Xiao Kunlin, Lu Mengnan, Huo Xinyu, Sun Mengyao, Yang Zhi, Wang Zhiyuan, Zhang Weijie, Zhi Liqiang, Meng Ziang, Ma Jie, Ma Jianbing, Zhang Rui

机构信息

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

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

出版信息

J Clin Med. 2023 Feb 7;12(4):1313. doi: 10.3390/jcm12041313.

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.

摘要

骨关节炎(OA)是最常见的关节炎类型,是一种与年龄相关的疾病,其特征是关节软骨进行性退化、滑膜炎症和软骨下骨退化。软骨细胞增殖受印度刺猬信号分子(人类中的IHH,动物中的Ihh)调节,该信号分子在骨骼系统发育过程中调节肥大和软骨内骨化。微小RNA(miRNA,miR)是一类约22个核苷酸的内源性非编码RNA,可负向调节基因表达。在本研究中,OA患者受损关节软骨组织和OA细胞培养物中IHH的表达水平上调,而miR-199a-5p的表达水平则相反。进一步研究表明,miR-199a-5p可直接调节IHH表达,并通过原发性人软骨细胞中的IHH信号通路减少软骨细胞肥大和基质降解。关节内注射合成的miR-199a-5p激动剂可减轻大鼠OA症状,包括减轻关节软骨破坏、软骨下骨退化和滑膜炎症。miR-199a-5p激动剂在体内也可抑制Ihh信号通路。本研究可能有助于理解miR-199a-5p在OA病理生理学和分子机制中的作用,并为OA患者指明一种潜在的新治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4df4/9959662/c39f90f9ab06/jcm-12-01313-g001.jpg

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