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骨关节炎发病机制的当前认识及相关新方法。

Current understanding of osteoarthritis pathogenesis and relevant new approaches.

作者信息

Tong Liping, Yu Huan, Huang Xingyun, Shen Jie, Xiao Guozhi, Chen Lin, Wang Huaiyu, Xing Lianping, Chen Di

机构信息

Research Center for Computer-aided Drug Discovery, Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, 518005, China.

Faculty of Pharmaceutical Sciences, Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, 518055, China.

出版信息

Bone Res. 2022 Sep 20;10(1):60. doi: 10.1038/s41413-022-00226-9.

DOI:10.1038/s41413-022-00226-9
PMID:36127328
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9489702/
Abstract

Osteoarthritis (OA) is the most common degenerative joint disease that causes painful swelling and permanent damage to the joints in the body. The molecular mechanisms of OA are currently unknown. OA is a heterogeneous disease that affects the entire joint, and multiple tissues are altered during OA development. To better understand the pathological mechanisms of OA, new approaches, methods, and techniques need to be used to understand OA pathogenesis. In this review, we first focus on the epigenetic regulation of OA, with a particular focus on DNA methylation, histone modification, and microRNA regulation, followed by a summary of several key mediators in OA-associated pain. We then introduce several innovative techniques that have been and will continue to be used in the fields of OA and OA-associated pain, such as CRISPR, scRNA sequencing, and lineage tracing. Next, we discuss the timely updates concerning cell death regulation in OA pathology, including pyroptosis, ferroptosis, and autophagy, as well as their individual roles in OA and potential molecular targets in treating OA. Finally, our review highlights new directions on the role of the synovial lymphatic system in OA. An improved understanding of OA pathogenesis will aid in the development of more specific and effective therapeutic interventions for OA.

摘要

骨关节炎(OA)是最常见的退行性关节疾病,会导致身体关节疼痛肿胀并造成永久性损伤。目前,OA的分子机制尚不清楚。OA是一种影响整个关节的异质性疾病,在OA发展过程中多个组织会发生改变。为了更好地理解OA的病理机制,需要采用新的方法和技术来了解OA的发病机制。在本综述中,我们首先关注OA的表观遗传调控,特别关注DNA甲基化、组蛋白修饰和微小RNA调控,接着总结OA相关疼痛中的几种关键介质。然后,我们介绍一些已在OA及OA相关疼痛领域使用并将继续使用的创新技术,如CRISPR、单细胞RNA测序和谱系追踪。接下来,我们讨论OA病理学中细胞死亡调控的最新进展,包括细胞焦亡、铁死亡和自噬,以及它们在OA中的各自作用和治疗OA的潜在分子靶点。最后,我们的综述强调了滑膜淋巴系统在OA中的作用的新方向。对OA发病机制的深入理解将有助于开发更具特异性和有效性的OA治疗干预措施。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b162/9489702/7545699428ef/41413_2022_226_Fig6_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b162/9489702/7545699428ef/41413_2022_226_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b162/9489702/d5ebf1deb5e6/41413_2022_226_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b162/9489702/1745afc3edb0/41413_2022_226_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b162/9489702/41923b4f1560/41413_2022_226_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b162/9489702/539c2176a935/41413_2022_226_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b162/9489702/cb8eea83801a/41413_2022_226_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b162/9489702/7545699428ef/41413_2022_226_Fig6_HTML.jpg

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