Cystatin C is a disease-associated protein subject to multiple regulation

被引:87
作者
Xu, Yuekang [1 ]
Ding, Ying [1 ]
Li, Xinchen [1 ]
Wu, Xiaobing [1 ]
机构
[1] Anhui Normal Univ, Sch Life Sci, Anhui Prov Key Lab Conservat & Exploitat Biol Res, Wuhu 241000, Anhui, Peoples R China
基金
英国医学研究理事会;
关键词
GLOMERULAR-FILTRATION-RATE; EXPERIMENTAL SUBARACHNOID HEMORRHAGE; HEREDITARY CEREBRAL-HEMORRHAGE; TEMPORAL-LOBE EPILEPSY; RETRACTED ARTICLE. SEE; GROWTH-FACTOR-BETA; E-DEFICIENT MICE; DENDRITIC CELLS; AMYLOID ANGIOPATHY; IN-VITRO;
D O I
10.1038/icb.2014.121
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
A protease inhibitor, cystatin C (Cst C), is a secreted cysteine protease inhibitor abundantly expressed in body fluids. Clinically, it is mostly used to measure glomerular filtration rate as a marker for kidney function due to its relatively small molecular weight and easy detection. However, recent findings suggest that Cst C is regulated at both transcriptional and post-translational levels, and Cst C production from haematopoietic cell lineages contributes significantly to the systematic pools of Cst C. Furthermore, Cst C is directly linked to many pathologic processes through various mechanisms. Thus fluctuation of Cst C levels might have serious clinical implications rather than a mere reflection of kidney functions. Here, we summarize the pathophysiological roles of Cst C dependent and independent on its inhibition of proteases, outline its change of expression by various stimuli, and elucidate the regulatory mechanisms to control this disease-related protease inhibitor. Finally, we discuss the clinical implications of these findings for translational gains.
引用
收藏
页码:442 / 451
页数:10
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