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CB1大麻素受体的组成型内吞循环

Constitutive endocytic cycle of the CB1 cannabinoid receptor.

作者信息

Leterrier Christophe, Bonnard Damien, Carrel Damien, Rossier Jean, Lenkei Zsolt

机构信息

ESPCI-CNRS UMR 7637, Laboratoire Neurobiologie et Diversité Cellulaire, Ecole Supérieure de Physique et de Chimie Industrielles, 10 Rue Vauquelin, 75231 Paris Cedex 05, France.

出版信息

J Biol Chem. 2004 Aug 20;279(34):36013-21. doi: 10.1074/jbc.M403990200. Epub 2004 Jun 21.

Abstract

The CB1 cannabinoid receptor (CB1R) displays a significant level of ligand-independent (i.e. constitutive) activity, either when heterologously expressed in nonneuronal cells or in neurons where CB1Rs are endogenous. The present study investigates the consequences of constitutive activity on the intracellular trafficking of CB1R. When transfected in HEK-293 cells, CB1R is present at the plasma membrane, but a substantial proportion ( approximately 85%) of receptors is localized in intracellular vesicles. Detailed analysis of CB1-EGFP expressed in HEK-293 cells shows that the intracellular CB1R population is mostly of endocytic origin and that treatment with inverse agonist AM281 traps CB1R at the plasma membrane through a monensin-sensitive recycling pathway. Co-transfection with dominant positive or dominant negative mutants of the small GTPases Rab5 and Rab4, but not Rab11, profoundly modifies the steady-state and ligand-induced intracellular distribution of CB1R, indicating that constitutive endocytosis is Rab5-dependent, whereas constitutive recycling is mediated by Rab4. In conclusion, our results indicate that, due to its natural constitutive activity, CB1R permanently and constitutively cycles between plasma membrane and endosomes, leading to a predominantly intracellular localization at steady state.

摘要

CB1大麻素受体(CB1R)无论是在非神经元细胞中异源表达,还是在CB1R为内源性的神经元中,都表现出显著水平的非配体依赖性(即组成性)活性。本研究探讨了组成性活性对CB1R细胞内转运的影响。当转染到HEK - 293细胞中时,CB1R存在于质膜上,但相当一部分(约85%)的受体定位于细胞内囊泡中。对在HEK - 293细胞中表达的CB1 - EGFP的详细分析表明,细胞内的CB1R群体大多来源于内吞作用,并且用反向激动剂AM281处理可通过莫能菌素敏感的再循环途径将CB1R捕获在质膜上。与小GTP酶Rab5和Rab4的显性阳性或显性阴性突变体共转染,但不与Rab11共转染,会深刻改变CB1R的稳态和配体诱导的细胞内分布,表明组成性内吞作用依赖于Rab5,而组成性再循环由Rab4介导。总之,我们的结果表明,由于其天然的组成性活性,CB1R在质膜和内体之间永久且组成性地循环,导致在稳态下主要定位于细胞内。

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