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趋化因子受体细胞内转运。

Chemokine receptors intracellular trafficking.

机构信息

Department of Translational Medicine, University of Milan, I-20089 Rozzano, Milan, Italy.

出版信息

Pharmacol Ther. 2010 Jul;127(1):1-8. doi: 10.1016/j.pharmthera.2010.04.006. Epub 2010 May 6.

Abstract

Chemokines coordinate leukocyte recruitment during inflammatory and immune responses through the interaction with a distinct subfamily of G protein-coupled receptors. The magnitude of the cellular response elicited by chemokines is dictated by the level of receptor expression at the plasma membrane, which is the balance of finely tuned endocytic and recycling pathways. Recent data have revealed that receptor trafficking properties can drive chemokine receptors to lysosomal degradation or recycling pathways, producing opposite effects on the strength of the intracellular signaling cascade. This review will cover recent advances on the molecular mechanisms underlying chemokine receptor internalization, recycling and degradation pathways, with particular attention to structural motifs present in receptor intracellular domains and their interacting adaptor proteins that modulate receptor trafficking and dictate proper biological response.

摘要

趋化因子通过与 G 蛋白偶联受体的一个独特亚家族相互作用,在炎症和免疫反应中协调白细胞募集。趋化因子引起的细胞反应的大小取决于质膜上受体的表达水平,这是精细调节的内吞和回收途径的平衡。最近的数据表明,受体运输特性可以将趋化因子受体导向溶酶体降解或回收途径,从而对细胞内信号级联反应的强度产生相反的影响。这篇综述将涵盖趋化因子受体内化、回收和降解途径的分子机制的最新进展,特别关注受体细胞内结构域中的结构基序及其相互作用的衔接蛋白,这些基序和蛋白调节受体运输并决定适当的生物学反应。

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