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小窝在心脏保护中的作用。

Role of caveolae in cardiac protection.

作者信息

Roth David M, Patel Hemal H

机构信息

VA Medical Center (125), Veterans Affairs San Diego Healthcare System, 3350 La Jolla Village Drive, San Diego, CA 92161-5085, USA.

出版信息

Pediatr Cardiol. 2011 Mar;32(3):329-33. doi: 10.1007/s00246-010-9881-8. Epub 2011 Jan 6.

Abstract

Myocardial ischemia/reperfusion injury is a major cause of morbidity and mortality. The molecular signaling pathways involved in cardiac protection from myocardial ischemia/reperfusion injury are complex. An emerging idea in signal transduction suggests the existence of spatially organized complexes of signaling molecules in lipid-rich microdomains of the plasma membrane known as caveolae. Caveolins-proteins abundant in caveolae-provide a scaffold to organize, traffic, and regulate signaling molecules. Numerous signaling molecules involved in cardiac protection are known to exist within caveolae or interact directly with caveolins. Over the last 4 years, our laboratories have explored the hypothesis that caveolae are vitally important to cardiac protection from myocardial ischemia/reperfusion injury. We have provided evidence that (1) caveolae and the caveolin isoforms 1 and 3 are essential for cardiac protection from myocardial ischemia/reperfusion injury, (2) stimuli that produce preconditioning of cardiac myocytes, including brief periods of ischemia/reperfusion and exposure to volatile anesthetics, alter the number of membrane caveolae, and (3) cardiac myocyte-specific overexpression of caveolin-3 can produce innate cardiac protection from myocardial ischemia/reperfusion injury. The work demonstrates that caveolae and caveolins are critical elements of signaling pathways involved in cardiac protection and suggests that caveolins are unique targets for therapy in patients at risk of myocardial ischemia.

摘要

心肌缺血/再灌注损伤是发病和死亡的主要原因。参与心脏保护免受心肌缺血/再灌注损伤的分子信号通路很复杂。信号转导领域一个新出现的观点认为,在质膜富含脂质的微区(称为小窝)中存在信号分子的空间组织化复合物。小窝蛋白(小窝中丰富的蛋白质)为组织、运输和调节信号分子提供了一个支架。已知许多参与心脏保护的信号分子存在于小窝内或直接与小窝蛋白相互作用。在过去4年里,我们实验室探讨了小窝对心脏保护免受心肌缺血/再灌注损伤至关重要这一假说。我们提供的证据表明:(1)小窝以及小窝蛋白亚型1和3对心脏保护免受心肌缺血/再灌注损伤至关重要;(2)能使心肌细胞产生预处理的刺激,包括短暂的缺血/再灌注和暴露于挥发性麻醉剂,会改变细胞膜小窝的数量;(3)心肌细胞特异性过表达小窝蛋白-3可产生先天性心脏保护,使其免受心肌缺血/再灌注损伤。这项工作表明,小窝和小窝蛋白是参与心脏保护的信号通路的关键要素,并提示小窝蛋白是有心肌缺血风险患者治疗的独特靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4308/3051068/bb50420cca09/246_2010_9881_Fig1_HTML.jpg

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