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G蛋白偶联受体转运的调控

Regulation of G protein-coupled receptor trafficking.

作者信息

Xu Z-Q D, Zhang X, Scott L

机构信息

Department of Neuroscience, Karolinska Institutet, Stockholm, Sweden.

出版信息

Acta Physiol (Oxf). 2007 May;190(1):39-45. doi: 10.1111/j.1365-201X.2007.01695.x.

Abstract

G protein-coupled receptors (GPCRs) mediate cellular responses to diverse extracellular stimuli to play a vital role in the control of physiology and behaviour. GPCR trafficking is of fundamental importance for the regulation of GPCRs signaling. In this mini review, we will discuss some of the recent findings on the mechanisms that regulate GPCR trafficking, which include (i) large dense-core vesicle (LDCV)-associated GPCR delivery which could be a general cell biological mechanism for rapid modulation of membrane receptors in response to certain stimuli; (ii) lateral diffusion of GPCRs in the plasma membrane for rapid change of the number of neurotransmitter receptors during synaptic plasticity and (iii) constitutive internalization of GPCRs, that contributes to receptor resensitization and distribution, including axonal polarization.

摘要

G蛋白偶联受体(GPCRs)介导细胞对多种细胞外刺激的反应,在生理和行为控制中发挥着至关重要的作用。GPCR的运输对于GPCR信号传导的调节至关重要。在本综述中,我们将讨论一些关于调节GPCR运输机制的最新发现,其中包括:(i)与大致密核心囊泡(LDCV)相关的GPCR递送,这可能是一种普遍的细胞生物学机制,用于响应某些刺激快速调节膜受体;(ii)GPCR在质膜中的侧向扩散,用于在突触可塑性期间快速改变神经递质受体的数量;以及(iii)GPCR的组成型内化,这有助于受体重新敏感化和分布,包括轴突极化。

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