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Role of Caveolae in Cardiac Protection

机译:小窝蛋白在心脏保护中的作用

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摘要

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.
机译:心肌缺血/再灌注损伤是发病率和死亡率的主要原因。涉及心脏保护免受心肌缺血/再灌注损伤的分子信号传导途径是复杂的。信号转导中的一个新兴想法表明,在称为小窝的质膜富含脂质的微区中存在信号分子的空间组织复合物。洞穴蛋白(caveolae中富含的蛋白质)提供了一个组织,运输和调节信号分子的支架。已知参与心脏保护的多种信号分子存在于小窝内或直接与小窝相互作用。在过去的四年中,我们的实验室探索了以下假设,即小孔洞对于保护心脏免受心肌缺血/再灌注损伤至关重要。我们已经提供了证据,(1)小窝蛋白和小窝蛋白同工型1和3对于心肌免受心肌缺血/再灌注损伤的心脏保护至关重要,(2)产生心肌细胞预处理的刺激,包括短暂的缺血/再灌注和暴露于挥发性物质麻醉药,改变膜小窝的数量和(3)心肌特异性小窝蛋白3的过度表达可产生先天性心脏保护,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,并表明小窝蛋白是具有心肌缺血风险的患者治疗的独特靶标。

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