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跑步后跟腱中的胶原蛋白变性与跟腱病:体内机械生理学与磁共振成像

Collagen denaturation in post-run Achilles tendons and Achilles tendinopathy: In vivo mechanophysiology and magnetic resonance imaging.

作者信息

Fang Yijie, Zhu Dantian, Wei Jingyue, Qian Lei, Qiu Rongmao, Jia Taoyu, Huang Kui, Zhao Suwen, Ouyang Jun, Li Man, Li Shaolin, Li Yang

机构信息

Department of Radiology, Guangdong Provincial Engineering Research Center of Molecular Imaging, Guangdong-Hong Kong-Macao University Joint Laboratory of Interventional Medicine, the Fifth Affiliated Hospital, Sun Yat-sen University, Zhuhai, Guangdong 519000, China.

Guangdong Provincial Engineering Research Center of Molecular Imaging, Biobank, Department of Information Technology and Data Center, the Fifth Affiliated Hospital, Sun Yat-sen University, Zhuhai, Guangdong 519000, China.

出版信息

Sci Adv. 2024 Oct 4;10(40):eado2015. doi: 10.1126/sciadv.ado2015. Epub 2024 Oct 2.

Abstract

Achilles tendinopathy is often attributed to overuse, but its pathophysiology remains poorly understood. Disruption to the molecular structure of collagen is fundamental for the onset and progression of tendinopathy but has mostly been investigated in vitro. Here, we interrogated the in vivo molecular structure changes of collagen in rat Achilles tendons following treadmill running. Unexpectedly, the tendons' collagen molecules were not mechanically unfolded by running but denatured through proteolysis during physiological post-run remodeling. We further revealed that running induces inflammatory gene expressions in Achilles tendons and that long-term running causes prolonged, elevated collagen degradation, leading to the accumulation of denatured collagen and tendinopathy development. For applications, we demonstrated magnetic resonance imaging of collagenase-induced Achilles tendon injury in vivo using a denatured collagen targeting contrast agent. Our findings may help close the knowledge gaps in the mechanobiology and pathogenesis of Achilles tendinopathy and initiate new strategies for its imaging-based diagnosis.

摘要

跟腱病通常被认为是过度使用所致,但其病理生理学仍知之甚少。胶原蛋白分子结构的破坏是肌腱病发生和发展的根本原因,但大多是在体外进行研究的。在此,我们研究了大鼠跟腱在跑步机跑步后体内胶原蛋白的分子结构变化。出乎意料的是,肌腱的胶原蛋白分子并非因跑步而机械性展开,而是在生理状态下跑步后的重塑过程中通过蛋白水解作用变性。我们进一步发现,跑步会诱导跟腱中的炎症基因表达,长期跑步会导致胶原蛋白降解延长且加剧,从而导致变性胶原蛋白的积累和跟腱病的发展。在应用方面,我们使用一种靶向变性胶原蛋白的造影剂,在体内对胶原酶诱导的跟腱损伤进行了磁共振成像。我们的研究结果可能有助于填补跟腱病机械生物学和发病机制方面的知识空白,并启动基于成像的诊断新策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a0d/11446262/89547808f5e7/sciadv.ado2015-f1.jpg

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