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脑血管疾病中的胱抑素C

Cystatin C in Cerebrovascular Disorders.

作者信息

Zhang Yaru, Sun Li

机构信息

Department of Neurology and Neuroscience Center, The First Hospital of Jilin University, Changchun, China.

出版信息

Curr Neurovasc Res. 2017;14(4):406-414. doi: 10.2174/1567202614666171116102504.

Abstract

Cystatin C (CysC), a cysteine protease inhibitor, has been widely proven to be a highly sensitive biomarker to predict the kidney function. The similarity of the renal and cerebral small vessels has awakened a surge of studies suggesting that CysC plays a key role in various cerebrovascular disorders. This review focuses on four major mechanisms of CysC in a variety of cerebrovascular diseases. (1) The property of the CysC Leu-68-Gln (L68Q) variant to aggregate and the property of the wild type CysC protein to co-aggregate with Amyloid-β (Aβ); (2) The disruption of equilibrium between CysC and related cysteine proteases; (3) The function of CysC as an inflammatory inducing factor; (4) The ability of CysC to induce autophagy. The combination of these CysC properties provides a well-supported novel biomarker for cerebrovascular diseases.

摘要

胱抑素C(CysC)是一种半胱氨酸蛋白酶抑制剂,已被广泛证明是预测肾功能的高敏感性生物标志物。肾小血管和脑小血管的相似性引发了大量研究,表明CysC在各种脑血管疾病中起关键作用。本综述重点关注CysC在多种脑血管疾病中的四种主要机制。(1)CysC亮氨酸-68-谷氨酰胺(L68Q)变体的聚集特性以及野生型CysC蛋白与淀粉样β蛋白(Aβ)共聚集的特性;(2)CysC与相关半胱氨酸蛋白酶之间平衡的破坏;(3)CysC作为炎症诱导因子的功能;(4)CysC诱导自噬的能力。这些CysC特性的结合为脑血管疾病提供了一个有充分依据的新型生物标志物。

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