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GRK2 在细胞代谢的控制轴上。

GRK2 at the control shaft of cellular metabolism.

机构信息

Department of Clinical Medicine and Cardiovascular Science, "Federico II" University of Naples, Italy.

出版信息

Curr Pharm Des. 2012;18(2):121-7. doi: 10.2174/138161212799040493.

Abstract

G protein receptor kinase 2 (GRK2) has been for years mainly considered the negative regulator of the cardiac β adrenergic signaling. However GRK2 is a ubiquitous molecule and its kinase activity and scaffold properties brought to several investigations which have evidenced its involvement in pathophysiology of extra-cardiac diseases. Later discoveries, moreover, indicated that this molecule is also able to influence other pathways such as insulin signaling by an inhibitory role similar to what described years before on βAR signaling. The importance of this novel function is in particular related to the possibility that this molecule can regulate the cellular metabolism, modifying the ability of cells to utilize different substrates. This hypothesis has been recently investigated in animal model of Heart Failure, evidencing that upregulation of GRK2 leads to alterations of cardiac glucose metabolism in the early stages of the disease. However GRK2 shows increased level also in the early stages of others chronic disease such as Alzheimer's Disease, indicating that these findings could be possibly applied to others cellular system and supporting the emerging idea of GRK2 as master regulator of cellular metabolism.

摘要

G 蛋白偶联受体激酶 2(GRK2)多年来主要被认为是心脏β肾上腺素能信号的负调节剂。然而,GRK2 是一种普遍存在的分子,其激酶活性和支架特性使其参与了多种研究,这些研究证实了它在心脏外疾病的病理生理学中的作用。此外,后来的发现表明,这种分子还能够通过类似于多年前描述的βAR 信号的抑制作用来影响其他途径,如胰岛素信号。这种新功能的重要性特别与该分子能够调节细胞代谢、改变细胞利用不同底物的能力的可能性有关。这一假设最近在心力衰竭的动物模型中进行了研究,结果表明,GRK2 的上调导致疾病早期心脏葡萄糖代谢的改变。然而,GRK2 在阿尔茨海默病等其他慢性疾病的早期阶段也显示出更高的水平,这表明这些发现可能适用于其他细胞系统,并支持将 GRK2 作为细胞代谢的主要调节剂的新兴观点。

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