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Mechanisms linking mitochondrial mechanotransduction and chondrocyte biology in the pathogenesis of osteoarthritis.

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机构: [a]Department of Orthopaedics, Nanfang Hospital, Southern Medical University, Guangzhou, 510515, China [b]Guangdong Engineering Research Center for Translation of Medical 3D Printing Application, Guangdong Provincial Key Laboratory of Medical Biomechanics, School of Basic Medical Sciences, Southern Medical University, Guangzhou, 510515, China [c]Guangdong Medical Innovation Platform for Translation of 3D Printing Application, The Third Affiliated Hospital of Southern Medical University, Southern Medical University, Guangzhou, 510515, China [d]Department of Orthopaedics, Affiliated Traditional Chinese Medicine Hospital, Southwest Medical University, Luzhou, 646000, China [e]Shunde Hospital, Southern Medical University (The First People’s Hospital of Shunde), Foshan, 528308, China [f]Orthopaedic Center, Affiliated Hospital of Guangdong Medical University, Guangdong Medical University, Zhanjiang, 524000, China
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Mechanical loading is essential for chondrocyte health. Chondrocytes can sense and respond to various extracellular mechanical signals through an integrated set of mechanisms. Recently, it has been found that mitochondria, acting as critical mechanotransducers, are at the intersection between extracellular mechanical signals and chondrocyte biology. Much attention has been focused on identifying how mechanical loading-induced mitochondrial dysfunction contributes to the pathogenesis of osteoarthritis. In contrast, little is known regarding the mechanisms underlying functional alterations in mitochondria induced by mechanical stimulation. In this review, we describe how chondrocytes perceive environmental mechanical signals. We discuss how mechanical load induces mitochondrial functional alterations and highlight the major unanswered questions in this field. We speculate that AMP-activated protein kinase (AMPK), a master regulator of energy homeostasis, may play an important role in coupling force transmission to mitochondrial health and intracellular biological responses. Copyright © 2021. Published by Elsevier B.V.

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出版当年[2020]版
大类 | 1 区 医学
小类 | 1 区 老年医学 2 区 细胞生物学
最新[2025]版
大类 | 1 区 医学
小类 | 1 区 老年医学 2 区 细胞生物学
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第一作者机构: [a]Department of Orthopaedics, Nanfang Hospital, Southern Medical University, Guangzhou, 510515, China
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通讯机构: [a]Department of Orthopaedics, Nanfang Hospital, Southern Medical University, Guangzhou, 510515, China [b]Guangdong Engineering Research Center for Translation of Medical 3D Printing Application, Guangdong Provincial Key Laboratory of Medical Biomechanics, School of Basic Medical Sciences, Southern Medical University, Guangzhou, 510515, China [c]Guangdong Medical Innovation Platform for Translation of 3D Printing Application, The Third Affiliated Hospital of Southern Medical University, Southern Medical University, Guangzhou, 510515, China [f]Orthopaedic Center, Affiliated Hospital of Guangdong Medical University, Guangdong Medical University, Zhanjiang, 524000, China [*1]Guangdong Engineering Research Center for Translation of Medical 3D Printing Application, Guangdong Provincial Key Laboratory of Medical Biomechanics, School of Basic Medical Sciences, Southern Medical University, Guangzhou, 510515, China [*2]Department of Orthopaedics, Nanfang Hospital, Southern Medical University, Guangzhou, 510515, China
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