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利用一组化学试剂研究破骨细胞形成和骨丢失过程中破骨细胞组织蛋白酶 K 的活性。

Investigation of osteoclast cathepsin K activity in osteoclastogenesis and bone loss using a set of chemical reagents.

机构信息

Department of Chemical Biology and Bioimaging, Wroclaw University of Science and Technology, Wyb. Wyspianskiego 27, 50-370 Wroclaw, Poland.

Department of Microbiology, Faculty of Biochemistry, Biophysics, and Biotechnology, Jagiellonian University, ul. Gronostajowa 7, 30-387 Kraków, Poland.

出版信息

Cell Chem Biol. 2023 Feb 16;30(2):159-174.e8. doi: 10.1016/j.chembiol.2023.01.001. Epub 2023 Jan 24.

Abstract

Cathepsin K (CatK) is a lysosomal cysteine protease whose highest expression is found in osteoclasts, which are the cells responsible for bone resorption. Investigations of the functions and physiological relevance of CatK have often relied on antibody-related techniques, which makes studying its activity patterns a challenging task. Hence, we developed a set of chemical tools for the investigation of CatK activity. We show that our probe is a valuable tool for monitoring the proteolytic activation of CatK during osteoclast formation. Moreover, we demonstrate that our inhibitor of CatK impedes osteoclastogenesis and bone resorption and that CatK is stored in its active form in osteoclasts within their lysosomal compartment and mainly in the ruffled borders of osteoclasts. Given that our probe recognizes active CatK within living cells without exhibiting any observed cytotoxicity in the several models tested, we expect that it would be well suited to theranostic applications in CatK-related diseases.

摘要

组织蛋白酶 K(CatK)是一种溶酶体半胱氨酸蛋白酶,其在破骨细胞中表达最高,破骨细胞是负责骨吸收的细胞。对 CatK 的功能和生理相关性的研究往往依赖于抗体相关技术,这使得研究其活性模式成为一项具有挑战性的任务。因此,我们开发了一组用于研究 CatK 活性的化学工具。我们表明,我们的探针是监测破骨细胞形成过程中 CatK 蛋白水解激活的有用工具。此外,我们证明我们的 CatK 抑制剂抑制破骨细胞生成和骨吸收,并且 CatK 以其活性形式储存在破骨细胞的溶酶体隔室中,主要存在于破骨细胞的皱褶缘中。鉴于我们的探针在没有观察到任何细胞毒性的情况下在几种测试模型中识别活细胞内的活性 CatK,我们预计它将非常适合与 CatK 相关疾病的治疗诊断应用。

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