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1-磷酸鞘氨醇通过Edg受体激活核因子-κB。在人胚肾293细胞中通过Edg-3和Edg-5激活,而非通过Edg-1激活。

Sphingosine 1-phosphate activates nuclear factor-kappa B through Edg receptors. Activation through Edg-3 and Edg-5, but not Edg-1, in human embryonic kidney 293 cells.

作者信息

Siehler S, Wang Y, Fan X, Windh R T, Manning D R

机构信息

Department of Pharmacology, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104, USA.

出版信息

J Biol Chem. 2001 Dec 28;276(52):48733-9. doi: 10.1074/jbc.M011072200. Epub 2001 Oct 22.

Abstract

Sphingosine 1-phosphate (S1P) exerts a variety of actions as a second messenger or as an agonist that binds to one or more members of the Edg family of G protein-coupled receptors. By using human embryonic kidney 293 cells, we show that S1P activates nuclear factor-kappa B (NF-kappa B) in a receptor-dependent fashion. Edg-3 and Edg-5, which are coupled to G(i), G(q), and G(13), affect activation of NF-kappa B, whereas Edg-1, which is coupled to G(i) alone, does not. We find that the activation of NF-kappa B requires protein kinase C and Ca(2+), probably downstream of G(q), but that the activation of Rho alone by S1P, whether through G(q) or G(13), does not translate into the activation of NF-kappa B. G beta gamma has little effect of its own but potentiates the activation of NF-kappa B achieved through other G proteins. We conclude that the activation of NF-kappa B by S1P is a receptor-mediated process that relies primarily on the activation of a phospholipase C by G(q) and secondarily on effector regulation through other G proteins.

摘要

1-磷酸鞘氨醇(S1P)作为第二信使或作为与G蛋白偶联受体的Edg家族的一个或多个成员结合的激动剂发挥多种作用。通过使用人胚肾293细胞,我们表明S1P以受体依赖的方式激活核因子-κB(NF-κB)。与G(i)、G(q)和G(13)偶联的Edg-3和Edg-5影响NF-κB的激活,而仅与G(i)偶联的Edg-1则不影响。我们发现NF-κB的激活需要蛋白激酶C和Ca(2+),可能在G(q)的下游,但S1P单独激活Rho,无论通过G(q)还是G(13),都不会转化为NF-κB的激活。Gβγ自身作用很小,但能增强通过其他G蛋白实现的NF-κB的激活。我们得出结论,S1P激活NF-κB是一个受体介导的过程,主要依赖于G(q)对磷脂酶C的激活,其次依赖于通过其他G蛋白的效应器调节。

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