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溶血磷脂酸的细胞间信号传导

Intercellular signaling by lysophosphatidate.

作者信息

Nietgen G W, Durieux M E

机构信息

Department of Anesthesiology, University of Virginia Health Sciences Center, Charlottesville 22908, USA.

出版信息

Cell Adhes Commun. 1998 Mar;5(3):221-35. doi: 10.3109/15419069809040293.

DOI:10.3109/15419069809040293
PMID:9686319
Abstract

Lysophosphatidate (LPA) is an intercellular phospholipid messenger with a wide range of biologic effects. The first discovered source of LPA in the human body were activated platelets, but several other sites of LPA generation are now known. The number of cellular interactions is also growing steadily and responses to the compound range wide, from induction of mitogenesis to neurite retraction. LPA acts via a specific G protein-coupled receptor, of which one or more subtypes may exist. Intracellularly, this receptor activates several heterotrimeric G proteins. LPA induces cell proliferation via the small GTP-binding proteins ras, and triggers actin-based cytoskeletal events through rho. This review describes the most relevant recent developments in our understanding of LPA signaling.

摘要

溶血磷脂酸(LPA)是一种具有广泛生物学效应的细胞间磷脂信使。人体中首次发现的LPA来源是活化的血小板,但现在已知还有其他几个LPA生成部位。细胞间相互作用的数量也在稳步增加,对该化合物的反应范围很广,从诱导有丝分裂到神经突回缩。LPA通过一种特定的G蛋白偶联受体发挥作用,可能存在一种或多种亚型。在细胞内,这种受体激活几种异源三聚体G蛋白。LPA通过小GTP结合蛋白ras诱导细胞增殖,并通过rho触发基于肌动蛋白的细胞骨架事件。本综述描述了我们对LPA信号传导理解方面最近最相关的进展。

相似文献

1
Intercellular signaling by lysophosphatidate.溶血磷脂酸的细胞间信号传导
Cell Adhes Commun. 1998 Mar;5(3):221-35. doi: 10.3109/15419069809040293.
2
Lysophosphatidic acid signalling.溶血磷脂酸信号传导
Curr Opin Cell Biol. 1995 Apr;7(2):203-10. doi: 10.1016/0955-0674(95)80029-8.
3
Development of our current understanding of bioactive lysophospholipids.我们目前对生物活性溶血磷脂认识的发展历程。
Ann N Y Acad Sci. 2000 Apr;905:1-10. doi: 10.1111/j.1749-6632.2000.tb06532.x.
4
Lysophosphatidic acid-induced neurite retraction in PC12 cells: neurite-protective effects of cyclic AMP signaling.溶血磷脂酸诱导PC12细胞神经突回缩:环磷酸腺苷信号通路的神经突保护作用
J Neurochem. 1996 Feb;66(2):549-58. doi: 10.1046/j.1471-4159.1996.66020549.x.
5
Exogenous phospholipase D generates lysophosphatidic acid and activates Ras, Rho and Ca2+ signaling pathways.外源性磷脂酶D可生成溶血磷脂酸并激活Ras、Rho和Ca2+信号通路。
Curr Biol. 1998 Mar 26;8(7):386-92. doi: 10.1016/s0960-9822(98)70157-5.
6
Sphingosine-1-phosphate rapidly induces Rho-dependent neurite retraction: action through a specific cell surface receptor.鞘氨醇-1-磷酸迅速诱导Rho依赖性神经突回缩:通过特定细胞表面受体发挥作用。
EMBO J. 1996 May 15;15(10):2388-92.
7
The Edg family G protein-coupled receptors for lysophospholipids: their signaling properties and biological activities.溶血磷脂的Edg家族G蛋白偶联受体:它们的信号传导特性和生物学活性。
J Biochem. 2002 Jun;131(6):767-71. doi: 10.1093/oxfordjournals.jbchem.a003163.
8
Lysophosphatidate-induced cell proliferation: identification and dissection of signaling pathways mediated by G proteins.溶血磷脂酸诱导的细胞增殖:G蛋白介导的信号通路的鉴定与剖析。
Cell. 1989 Oct 6;59(1):45-54. doi: 10.1016/0092-8674(89)90868-4.
9
Common signaling pathways link activation of murine PAR-1, LPA, and S1P receptors to proliferation of astrocytes.常见的信号通路将小鼠PAR-1、溶血磷脂酸(LPA)和1-磷酸鞘氨醇(S1P)受体的激活与星形胶质细胞的增殖联系起来。
Mol Pharmacol. 2003 Nov;64(5):1199-209. doi: 10.1124/mol.64.5.1199.
10
Activation of RhoA by lysophosphatidic acid and Galpha12/13 subunits in neuronal cells: induction of neurite retraction.溶血磷脂酸和Gα12/13亚基在神经元细胞中激活RhoA:诱导神经突回缩。
Mol Biol Cell. 1999 Jun;10(6):1851-7. doi: 10.1091/mbc.10.6.1851.

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