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整合素信号在关节发育、稳态和骨关节炎中的作用。

Integrin signalling in joint development, homeostasis and osteoarthritis.

机构信息

Cell Biology Section, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD, USA.

Craniofacial Anomalies and Regeneration Section, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD, USA.

出版信息

Nat Rev Rheumatol. 2024 Aug;20(8):492-509. doi: 10.1038/s41584-024-01130-8. Epub 2024 Jul 16.

Abstract

Integrins are key regulators of cell-matrix interactions during joint development and joint tissue homeostasis, as well as in the development of osteoarthritis (OA). The signalling cascades initiated by the interactions of integrins with a complex network of extracellular matrix (ECM) components and intracellular adaptor proteins orchestrate cellular responses necessary for maintaining joint tissue integrity. Dysregulated integrin signalling, triggered by matrix degradation products such as matrikines, disrupts this delicate balance, tipping the scales towards an environment conducive to OA pathogenesis. The interplay between integrin signalling and growth factor pathways further underscores the multifaceted nature of OA. Moreover, emerging insights into the role of endocytic trafficking in regulating integrin signalling add a new layer of complexity to the understanding of OA development. To harness the therapeutic potential of targeting integrins for mitigation of OA, comprehensive understanding of their molecular mechanisms across joint tissues is imperative. Ultimately, deciphering the complexities of integrin signalling will advance the ability to treat OA and alleviate its global burden.

摘要

整合素是关节发育和关节组织稳态过程中细胞-基质相互作用的关键调节剂,也是骨关节炎(OA)发展的关键调节剂。整合素与细胞外基质(ECM)成分和细胞内衔接蛋白组成的复杂网络相互作用所引发的信号级联反应,协调维持关节组织完整性所需的细胞反应。由基质降解产物(如基质细胞因子)触发的失调的整合素信号会破坏这种微妙的平衡,使 OA 发病机制的环境变得有利。整合素信号与生长因子通路之间的相互作用进一步强调了 OA 的多面性。此外,内吞运输在调节整合素信号中的作用的新见解为理解 OA 的发展增加了新的复杂性。为了利用靶向整合素来缓解 OA 的治疗潜力,必须全面了解它们在关节组织中的分子机制。最终,破译整合素信号的复杂性将提高治疗 OA 和减轻其全球负担的能力。

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