Osteoarthritis: Mechanistic Insights, Senescence, and Novel Therapeutic Opportunities.

IF 1.6 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Bioelectricity Pub Date : 2022-03-15 eCollection Date: 2022-03-01 DOI:10.1089/bioe.2021.0039
Paula Carpintero-Fernández, Marta Varela-Eirín, Alejandro García-Yuste, Iñaki López-Díaz, José Ramón Caeiro, María D Mayán
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引用次数: 0

Abstract

Osteoarthritis (OA) is the most common joint disease. In the last years, the research community has focused on understanding the molecular mechanisms that led to the pathogenesis of the disease, trying to identify different molecular and clinical phenotypes along with the discovery of new therapeutic opportunities. Different types of cell-to-cell communication mechanisms have been proposed to contribute to OA progression, including mechanisms mediated by connexin43 (Cx43) channels or by small extracellular vesicles. Furthermore, changes in the chondrocyte phenotype such as cellular senescence have been proposed as new contributors of the OA progression, changing the paradigm of the disease. The use of different drugs able to restore chondrocyte phenotype, to reduce cellular senescence and senescence-associated secretory phenotype components, and to modulate ion channel activity or Cx43 appears to be promising therapeutic strategies for the different types of OA. In this review, we aim to summarize the current knowledge in OA phenotypes related with aging and tissue damage and the new therapeutic opportunities currently available.

骨关节炎:机理认识、衰老和新的治疗机会。
骨关节炎(OA)是最常见的关节疾病。在过去几年中,研究界一直专注于了解导致该疾病发病的分子机制,试图确定不同的分子和临床表型,同时发现新的治疗机会。不同类型的细胞间通信机制被认为是导致 OA 进展的原因,其中包括由 connexin43(Cx43)通道或细胞外小泡介导的机制。此外,软骨细胞表型的变化(如细胞衰老)也被认为是导致 OA 进展的新因素,从而改变了这种疾病的模式。使用不同的药物来恢复软骨细胞表型、减少细胞衰老和衰老相关分泌表型成分、调节离子通道活性或 Cx43 似乎是治疗不同类型 OA 的有前途的策略。在这篇综述中,我们旨在总结与衰老和组织损伤相关的 OA 表型的现有知识,以及目前可用的新治疗机会。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Bioelectricity
Bioelectricity Multiple-
CiteScore
3.40
自引率
4.30%
发文量
33
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