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G蛋白偶联受体激酶4的新特性

Novel features of G protein-coupled receptor kinase 4.

作者信息

Neve Kim A

机构信息

Department of Behavioral Neuroscience, Oregon Health & Science University, Portland, USA.

出版信息

Mol Pharmacol. 2006 Mar;69(3):673-6. doi: 10.1124/mol.105.021535. Epub 2005 Dec 9.

Abstract

The defining characteristic of G protein-coupled receptor homologous desensitization is that the receptor must be occupied by an agonist or in an activated conformation that mimics an agonist-induced state. In most instances, the mechanistic basis for this characteristic is the high selectivity of G protein-coupled receptor kinases for the activated receptor. In this issue, Rankin et al. (p. 759) demonstrate that under some conditions, at least, the G protein-coupled receptor kinase GRK4 does not display a preference for the agonist-occupied D1 dopamine receptor. Coexpression of GRK4 and the D1 receptor in a heterologous system induces phosphorylation of the receptor in the absence of agonist, causing constitutive desensitization and internalization of the receptor. Lacking the normal rapid feedback mechanisms associated with homologous desensitization, a system incorporating constitutively active GRK4 will be prone to dysregulation, perhaps explaining the generally low expression of GRK4. Indeed, considerable evidence suggests that just such dysregulation resulting from mutationally activated GRK4 contributes to the heritable component of human essential hypertension (Physiol Genomics 19:223-246, 2004).

摘要

G蛋白偶联受体同源脱敏的决定性特征是,受体必须被激动剂占据或处于模拟激动剂诱导状态的活化构象。在大多数情况下,这一特征的机制基础是G蛋白偶联受体激酶对活化受体具有高度选择性。在本期杂志中,兰金等人(第759页)证明,至少在某些条件下,G蛋白偶联受体激酶GRK4对被激动剂占据的D1多巴胺受体没有偏好。在异源系统中共同表达GRK4和D1受体,在没有激动剂的情况下会诱导受体磷酸化,导致受体组成型脱敏和内化。缺乏与同源脱敏相关的正常快速反馈机制,包含组成型活性GRK4的系统将易于失调,这或许可以解释GRK4普遍低表达的原因。确实,大量证据表明,由突变激活的GRK4导致的这种失调是人类原发性高血压遗传成分的原因(《生理基因组学》19:223 - 246,2004年)。

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