von Zastrow Mark
Department of Psychiatry, University of California, San Francisco, Room N212E Genentech Hall, UCSF Mission Bay Campus, 600 16th Street, San Francisco, CA 94143-2140, USA.
Life Sci. 2003 Dec 5;74(2-3):217-24. doi: 10.1016/j.lfs.2003.09.008.
Endocytic membrane trafficking plays multiple roles in GPCR signaling and regulation. In the past several years much has been learned about molecular mechanisms that mediate and regulate endocytic trafficking of cloned GPCRs expressed in transfected cell lines, and there is accelerating progress toward elucidating the membrane trafficking of GPCRs in native tissues. Current views regarding ligand-induced endocytosis of adrenergic catecholamine and opioid neuropeptide receptors will be reviewed, focusing on recent data suggesting the existence of additional machinery controlling the endocytosis of specific GPCRs via clathrin-coated pits. Evidence that GPCRs are selectively 'sorted' between divergent downstream pathways after endocytosis will be discussed, focusing on recent insight to mechanisms controlling receptor sorting between distinct recycling and non-recycling membrane pathways.
内吞膜运输在G蛋白偶联受体(GPCR)信号传导和调节中发挥多种作用。在过去几年里,人们对介导和调节转染细胞系中表达的克隆GPCR内吞运输的分子机制有了很多了解,并且在阐明天然组织中GPCR的膜运输方面正在加速取得进展。本文将综述目前关于肾上腺素能儿茶酚胺和阿片类神经肽受体的配体诱导内吞作用的观点,重点关注最近的数据,这些数据表明存在通过网格蛋白包被小窝控制特定GPCR内吞作用的额外机制。将讨论GPCR在内吞后在不同下游途径之间被选择性“分选”的证据,重点关注最近对控制受体在不同循环和非循环膜途径之间分选机制的见解。