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激动剂调节的EDG-1受体向质膜小窝的靶向作用。鞘氨醇-1-磷酸对内皮型一氧化氮合酶的激活作用以及小窝蛋白-1在鞘脂信号转导中的作用。

Agonist-modulated targeting of the EDG-1 receptor to plasmalemmal caveolae. eNOS activation by sphingosine 1-phosphate and the role of caveolin-1 in sphingolipid signal transduction.

作者信息

Igarashi J, Michel T

机构信息

Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA.

出版信息

J Biol Chem. 2000 Oct 13;275(41):32363-70. doi: 10.1074/jbc.M003075200.

Abstract

Plasmalemmal caveolae are membrane microdomains that are specifically enriched in sphingolipids and contain a wide array of signaling proteins, including the endothelial isoform of nitric-oxide synthase (eNOS). EDG-1 is a G protein-coupled receptor for sphingosine 1-phosphate (S1P) that is expressed in endothelial cells and has been implicated in diverse vascular signal transduction pathways. We analyzed the subcellular distribution of EDG-1 in COS-7 cells transiently transfected with cDNA constructs encoding epitope-tagged EDG-1. Subcellular fractionation of cell lysates resolved by ultracentrifugation in discontinuous sucrose gradients revealed that approximately 55% of the EDG-1 protein was recovered in fractions enriched in caveolin-1, a resident protein of caveolae. Co-immunoprecipitation experiments showed that EDG-1 could be specifically precipitated by antibodies directed against caveolin-1 and vice versa. The targeting of EDG-1 to caveolae-enriched fractions was markedly increased (from 51 +/- 11% to 93 +/- 14%) by treatment of transfected cells with S1P (5 microm, 60 min). In co-transfection experiments expressing EDG-1 and eNOS cDNAs in COS-7 cells, we found that S1P treatment significantly and specifically increased nitric-oxide synthase activity, with an EC(50) of 30 nm S1P. Overexpression of transfected caveolin-1 cDNA together with EDG-1 and eNOS markedly diminished S1P-mediated eNOS activation; caveolin overexpression also attenuated agonist-induced phosphorylation of EDG-1 receptor by >90%. These results suggest that the interaction of the EDG-1 receptor with caveolin may serve to inhibit signaling through the S1P pathway, even as the targeting of EDG-1 to caveolae facilitates the interactions of this receptor with ligands and effectors that are also targeted to caveolae. The agonist-modulated targeting of EDG-1 to caveolae and its dynamic inhibitory interactions with caveolin identify new points for regulation of sphingolipid-dependent signaling in the vascular wall.

摘要

质膜小窝是富含鞘脂的膜微区,含有多种信号蛋白,包括内皮型一氧化氮合酶(eNOS)。EDG - 1是1 - 磷酸鞘氨醇(S1P)的G蛋白偶联受体,在内皮细胞中表达,参与多种血管信号转导途径。我们分析了用编码表位标记的EDG - 1的cDNA构建体瞬时转染的COS - 7细胞中EDG - 1的亚细胞分布。通过在不连续蔗糖梯度中进行超速离心对细胞裂解物进行亚细胞分级分离,结果显示约55%的EDG - 1蛋白存在于富含小窝蛋白 - 1(小窝的驻留蛋白)的组分中。免疫共沉淀实验表明,EDG - 1可被针对小窝蛋白 - 1的抗体特异性沉淀,反之亦然。用S1P(5 μmol,60分钟)处理转染细胞后,EDG - 1靶向富含小窝的组分的比例显著增加(从51±11%增加到93±14%)。在COS - 7细胞中共转染表达EDG - 1和eNOS cDNA的实验中,我们发现S1P处理显著且特异性地增加了一氧化氮合酶活性,S1P的EC50为30 nM。与EDG - 1和eNOS一起转染的小窝蛋白 - 1 cDNA的过表达显著降低了S1P介导的eNOS激活;小窝蛋白的过表达还使激动剂诱导的EDG - 1受体磷酸化减弱了90%以上。这些结果表明,EDG - 1受体与小窝蛋白的相互作用可能抑制通过S1P途径的信号传导,即使EDG - 1靶向小窝促进了该受体与同样靶向小窝的配体和效应器的相互作用。激动剂调节的EDG - 1向小窝的靶向及其与小窝蛋白的动态抑制性相互作用确定了血管壁中鞘脂依赖性信号传导调控的新位点。

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