| Literature DB >> 29149834 |
Yaru Zhang1, Li Sun1.
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. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.org.Entities:
Keywords: CysC; cerebral amyloid angiopathy (CAA); cerebral aneurysms (CAs); cerebral small vascular diseases (CSVDs); cerebrovascular diseases; ischemic stroke; subarachnoidzzm321990hemorrhage (SAH); vascular dementia (VD)
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Year: 2017 PMID: 29149834 DOI: 10.2174/1567202614666171116102504
Source DB: PubMed Journal: Curr Neurovasc Res ISSN: 1567-2026 Impact factor: 1.990