Choi Ji Woong, Lee Chang-Wook, Chun Jerold
Department of Molecular Biology, Helen L. Dorris Child and Adolescent Neuropsychiatric Disorder Institute, The Scripps Research Institute, 10550 North Torrey Pines Rd., ICND-118, La Jolla, CA 92037, USA.
Biochim Biophys Acta. 2008 Sep;1781(9):531-9. doi: 10.1016/j.bbalip.2008.03.004. Epub 2008 Mar 25.
Two lysophospholipids (LPs), lysophosphatidic acid (LPA) and sphingosine 1-phosphate (S1P), are known to affect various cellular events. Their actions are mediated by binding to at least ten bona fide high-affinity G protein-coupled receptors referred to as LPA1-5 and S1P1-5. These LPs are expressed throughout the body and are involved in a range of biological activities including normal development, as well as functioning in most organ systems. A growing number of biological functions have been uncovered in vivo using single- or multiple-null mice for each LP receptor. This review will focus on findings from in vivo as well as in vitro studies using genetic null mice for the LP receptors, LPA1,2,3 and S1P1,2,3,5, and for the LP producing enzymes, autotaxin and sphingosine kinase 1/2.
已知两种溶血磷脂(LPs),即溶血磷脂酸(LPA)和1-磷酸鞘氨醇(S1P),可影响多种细胞活动。它们的作用是通过与至少十种真正的高亲和力G蛋白偶联受体结合来介导的,这些受体被称为LPA1-5和S1P1-5。这些LPs在全身表达,并参与一系列生物活动,包括正常发育,以及在大多数器官系统中发挥作用。使用每种LP受体的单基因敲除或多基因敲除小鼠,在体内发现了越来越多的生物学功能。本综述将重点关注使用LP受体LPA1、2、3和S1P1、2、3、5以及LP产生酶自分泌运动因子和鞘氨醇激酶1/2的基因敲除小鼠进行的体内和体外研究结果。