Pyroptosis-related crosstalk in osteoarthritis: Macrophages, fibroblast-like synoviocytes and chondrocytes

IF 5.9 1区 医学 Q1 ORTHOPEDICS Journal of Orthopaedic Translation Pub Date : 2024-07-01 DOI:10.1016/j.jot.2024.06.014
Shida Kuang , Wen Sheng , Jiahao Meng , Weijie Liu , Yifan Xiao , Hang Tang , Xinying Fu , Min Kuang , Qinghu He , Shuguang Gao
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Abstract

The pathogenesis of osteoarthritis (OA) involves a multifaceted interplay of inflammatory processes. The initiation of pyroptosis involves the secretion of pro-inflammatory cytokines and has been identified as a critical factor in regulating the development of OA. Upon initiation of pyroptosis, a multitude of inflammatory mediators are released and can be disseminated throughout the synovial fluid within the joint cavity, thereby facilitating intercellular communication across the entire joint. The main cellular components of joints include chondrocytes (CC), fibroblast-like synoviocytes (FLS) and macrophages (MC). Investigating their interplay can enhance our understanding of OA pathogenesis. Therefore, we comprehensively examine the mechanisms underlying pyroptosis and specifically investigate the intercellular interactions associated with pyroptosis among these three cell types, thereby elucidating their collective contribution to the progression of OA. We propose the concept of ' CC-FLS-MC pyroptosis-related crosstalk', describe the various pathways of pyroptotic interactions among these three cell types, and focus on recent advances in intervening pyroptosis in these three cell types for treating OA. We hope this will provide a possible direction for diversification of treatment for OA.

The Translational potential of this article. The present study introduces the concept of ‘MC-FLS-CC pyroptosis-related crosstalk' and provides an overview of the mechanisms underlying pyroptosis, as well as the pathways through which it affects MC, FLS, and CC. In addition, the role of regulation of these three types of cellular pyroptosis in OA has also been concerned. This review offers novel insights into the interplay between these cell types, with the aim of providing a promising avenue for diversified management of OA.

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骨关节炎中与裂解相关的串联:巨噬细胞、纤维母细胞样滑膜细胞和软骨细胞
骨关节炎(OA)的发病机制涉及炎症过程的多方面相互作用。脓毒血症的启动涉及促炎细胞因子的分泌,已被确定为调节 OA 发展的关键因素。热渗透开始后,多种炎症介质会释放出来,并扩散到关节腔内的滑液中,从而促进整个关节的细胞间交流。关节的主要细胞成分包括软骨细胞(CC)、纤维母细胞样滑膜细胞(FLS)和巨噬细胞(MC)。研究它们之间的相互作用可以加深我们对 OA 发病机制的了解。因此,我们全面研究了热凋亡的内在机制,并特别研究了这三种细胞类型之间与热凋亡相关的细胞间相互作用,从而阐明它们对 OA 进展的共同贡献。我们提出了 "CC-FLS-MC 热昏迷相关串扰 "的概念,描述了这三种细胞间热昏迷相互作用的各种途径,并重点介绍了干预这三种细胞的热昏迷以治疗 OA 的最新进展。我们希望这将为OA的多样化治疗提供一个可能的方向。本研究提出了 "MC-FLS-CC热蛋白沉积相关串扰 "的概念,并概述了热蛋白沉积的机制及其影响MC、FLS和CC的途径。此外,还关注了这三种细胞热凋亡在 OA 中的调控作用。这篇综述对这些细胞类型之间的相互作用提出了新的见解,旨在为 OA 的多样化治疗提供一条前景广阔的途径。
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来源期刊
Journal of Orthopaedic Translation
Journal of Orthopaedic Translation Medicine-Orthopedics and Sports Medicine
CiteScore
11.80
自引率
13.60%
发文量
91
审稿时长
29 days
期刊介绍: The Journal of Orthopaedic Translation (JOT) is the official peer-reviewed, open access journal of the Chinese Speaking Orthopaedic Society (CSOS) and the International Chinese Musculoskeletal Research Society (ICMRS). It is published quarterly, in January, April, July and October, by Elsevier.
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