靶向p38 MAPK:内质网应激与年龄相关性骨质流失之间的潜在桥梁。

IF 4.4 2区 生物学 Q2 CELL BIOLOGY Cellular signalling Pub Date : 2024-12-07 DOI:10.1016/j.cellsig.2024.111549
Meng Yin , Xin Zheng , Liang Shi
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引用次数: 0

摘要

内质网(ER)在许多与年龄相关的骨骼疾病的发展中起着至关重要的作用。值得注意的是,内质网应激可以通过激活p38 MAPK通路,通过协调炎症反应、细胞凋亡和自噬来促进骨质流失。随着全球人口老龄化,与年龄相关的骨质流失疾病对社会和医疗保健造成了重大负担。本文综述了内质网应激激活的p38 MAPK在炎症、细胞凋亡和自噬中的重要作用,以及其对骨形成和骨吸收的影响。本文综述了内质网应激激活的p38 MAPK参与骨质疏松症、类风湿性关节炎、牙周炎和骨关节炎的分子机制,并讨论了靶向p38 MAPK的治疗潜力。此外,本文还对未来的研究方向进行了展望,为新的治疗策略提供了科学依据。
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Targeting p38 MAPK: A potential bridge between ER stress and age-related bone loss
The endoplasmic reticulum (ER) is crucial in the development of numerous age-related bone disorders. Notably, ER stress can precipitate bone loss by orchestrating inflammatory responses, apoptosis, and autophagy through the activation of the p38 MAPK pathway. Age-related bone loss diseases pose a significant burden on society and healthcare as the global population ages. This review provides a comprehensive analysis of recent research advancements, delving into the critical role of ER stress-activated p38 MAPK in inflammation, apoptosis, and autophagy, as well as its impact on bone formation and bone resorption. This review elucidates the molecular mechanisms underlying the involvement of ER stress-activated p38 MAPK in osteoporosis, rheumatoid arthritis, periodontitis, and osteoarthritis and discusses the therapeutic potential of targeting p38 MAPK. Furthermore, this review provides a scientific foundation for new therapeutic strategies by highlighting prospective research directions.
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来源期刊
Cellular signalling
Cellular signalling 生物-细胞生物学
CiteScore
8.40
自引率
0.00%
发文量
250
审稿时长
27 days
期刊介绍: Cellular Signalling publishes original research describing fundamental and clinical findings on the mechanisms, actions and structural components of cellular signalling systems in vitro and in vivo. Cellular Signalling aims at full length research papers defining signalling systems ranging from microorganisms to cells, tissues and higher organisms.
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