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钙蛋白酶介导的成骨细胞中骨量和脂肪量调节概述。

Overview of calpain-mediated regulation of bone and fat mass in osteoblasts.

机构信息

Endocrine Unit, Massachusetts General Hospital, Thier 10, 50 Blossom Street, Boston, MA 02114, USA.

出版信息

Cell Biochem Biophys. 2013 May;66(1):23-8. doi: 10.1007/s12013-012-9393-7.

Abstract

The receptor for parathyroid hormone (PTH) and PTH-related peptide (PTH1R) belongs to the class II G protein-coupled receptor superfamily. The calpain small subunit encoded by the gene Capns1 is the second protein and the first enzyme identified by a yeast two-hybrid screen using the intracellular C-terminal tail of the rat PTH1R. The calpain regulatory small subunit forms a heterodimer with the calpain large catalytic subunit and modulates various cellular functions as a cysteine protease. To investigate a physiological role of the calpain small subunit in cells of the osteoblast lineage, we generated osteoblast-specific Capns1 knockout mouse models and characterized their bone phenotype. Molecular mechanisms by which calpain modulates cell proliferation of the osteoblast lineage were further examined in vitro. Moreover, we utilized the mutant mice as a disease model of osteoporosis accompanied with impaired bone resorptive function and suggested a possible clinical translation of our basic research finding.

摘要

甲状旁腺激素(PTH)和 PTH 相关肽(PTH1R)受体属于 II 类 G 蛋白偶联受体超家族。该基因编码的钙蛋白酶小亚基 Capns1 是第二种蛋白,也是使用大鼠 PTH1R 细胞内 C 末端尾巴通过酵母双杂交筛选鉴定的第一种酶。钙蛋白酶调节小亚基与钙蛋白酶大催化亚基形成异二聚体,并作为半胱氨酸蛋白酶调节各种细胞功能。为了研究钙蛋白酶小亚基在成骨细胞系细胞中的生理作用,我们生成了成骨细胞特异性 Capns1 敲除小鼠模型,并对其骨骼表型进行了特征分析。在体外进一步研究了钙蛋白酶调节成骨细胞系细胞增殖的分子机制。此外,我们还利用突变小鼠作为骨质疏松症的疾病模型,其伴有受损的骨吸收功能,并提出了我们基础研究发现的可能的临床转化。

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引用本文的文献

本文引用的文献

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