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肩袖肌腱病中的组织蛋白酶:在人类慢性撕裂中的鉴定及在大鼠模型中的时间诱导

Cathepsins in Rotator Cuff Tendinopathy: Identification in Human Chronic Tears and Temporal Induction in a Rat Model.

作者信息

Seto Song P, Parks Akia N, Qiu Yongzhi, Soslowsky Louis J, Karas Spero, Platt Manu O, Temenoff Johnna S

机构信息

W.H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University, 313 Ferst Drive, Atlanta, GA, 30332, USA,

出版信息

Ann Biomed Eng. 2015 Sep;43(9):2036-46. doi: 10.1007/s10439-014-1245-8. Epub 2015 Jan 6.

Abstract

While overuse of the supraspinatus tendon is a leading factor in rotator cuff injury, the underlying biochemical changes have not been fully elucidated. In this study, torn human rotator cuff (supraspinatus) tendon tissue was analyzed for the presence of active cathepsin proteases with multiplex cysteine cathepsin zymography. In addition, an overuse injury to supraspinatus tendons was induced through downhill running in an established rat model. Histological analysis demonstrated that structural damage occurred by 8 weeks of overuse compared to control rats in the region of tendon insertion into bone. In both 4- and 8-week overuse groups, via zymography, there was approximately a 180% increase in cathepsin L activity at the insertion region compared to the controls, while no difference was found in the midsubstance area. Additionally, an over 400% increase in cathepsin K activity was observed for the insertion region of the 4-week overused tendons. More cathepsin K and L immunostaining was observed at the insertion region of the overuse groups compared to controls. These results provide important information on a yet unexplored mechanism for tendon degeneration that may operate alone or in conjunction with other proteases to contribute to chronic tendinopathy.

摘要

虽然冈上肌腱过度使用是肩袖损伤的主要因素,但潜在的生化变化尚未完全阐明。在本研究中,使用多重半胱氨酸组织蛋白酶酶谱分析法分析了撕裂的人肩袖(冈上肌)肌腱组织中活性组织蛋白酶的存在情况。此外,在已建立的大鼠模型中通过下坡跑诱导冈上肌腱过度使用损伤。组织学分析表明,与对照大鼠相比,在肌腱插入骨的区域,过度使用8周会导致结构损伤。在4周和8周的过度使用组中,通过酶谱分析发现,与对照组相比,插入区域组织蛋白酶L活性增加了约180%,而中间区域未发现差异。此外,在4周过度使用肌腱的插入区域观察到组织蛋白酶K活性增加超过400%。与对照组相比,在过度使用组的插入区域观察到更多的组织蛋白酶K和L免疫染色。这些结果为尚未探索的肌腱退变机制提供了重要信息,该机制可能单独起作用或与其他蛋白酶共同作用,导致慢性肌腱病。

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