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硫氧还蛋白
氧化应激
抗氧化剂
硫氧还蛋白相互作用蛋白
活性氧
炎症
细胞内
化学
氧化磷酸化
生物化学
氧化还原
细胞生物学
生物
免疫学
有机化学
作者
Ludivine Billiet,Mustapha Rouis
出处
期刊:Cardiovascular and Hematological Disorders - Drug Targets
[Bentham Science]
日期:2008-12-01
卷期号:8 (4): 293-296
被引量:9
标识
DOI:10.2174/187152908786786179
摘要
The regulation of cellular reduction/oxidation (redox) balance is critically determined by several antioxidant systems such as the thioredoxin-1 (Trx-1) which reduces disulfides on targeted proteins. In addition, intracellular Trx-1 exerts most of its antioxidant properties through scavenging of reactive oxygen species. Moreover, it acts as a cofactor for several enzymes and plays an important role in the regulation of redox-sensitive transcription factors. Several studies have reported that Trx-1 activity can be modulated by the interaction with vitamin D3-upregulated protein (VDUP-1) (also called Txnip for thioredoxin interacting protein-1 or TBP-2 for Trx-binding protein-2). Trx-1 secretion has been reported to occur in conditions associated with oxidative stress and inflammation. Beneficial effects of elevated plasma Trx-1 levels on various pathologies were reported in mice. In conclusion, oxidative stress is an important actor in various pathologies including cardio- and cerebro-vascular diseases. Therefore, controlling the redox status by increasing the activity of Trx-1 seems to be a novel and an attractive approach. Keywords: Thioredoxin, oxidative stress, antioxidant, inflammation, cardiovascular diseases
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