Kingsbury M A, Rehen S K, Ye X, Chun J
Department of Molecular Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, ICND 118, La Jolla, California 92037, USA.
J Cell Biochem. 2004 Aug 1;92(5):1004-12. doi: 10.1002/jcb.20061.
Lysophosphatidic acid (LPA) is a small lysophospholipid that signals through G-protein coupled receptors (GPCRs) to mediate diverse cellular responses. Two LPA receptors, LPA(1) and LPA(2), show gene expression profiles in mouse embryonic cerebral cortex, suggesting roles for LPA signaling in cerebral cortical development. Here, we review loss-of-function and gain-of-function models that have been used to examine LPA signaling. Genetic deletion of lpa(1) or both lpa(1) and lpa(2) in mice results in 50-65% neonatal lethality, but not obvious cortical phenotypes in survivors, suggesting that compensatory signaling systems exist for regulating cortical development. A gain-of-function model, approached by increasing receptor activation through exogenous delivery of LPA, shows that LPA signaling regulates cerebral cortical growth and anatomy by affecting proliferation, differentiation and cell survival during embryonic development.
溶血磷脂酸(LPA)是一种小的溶血磷脂,它通过G蛋白偶联受体(GPCRs)发出信号,介导多种细胞反应。两种LPA受体,LPA(1)和LPA(2),在小鼠胚胎大脑皮层中显示出基因表达谱,提示LPA信号在大脑皮层发育中发挥作用。在此,我们综述了用于研究LPA信号的功能丧失和功能获得模型。在小鼠中基因敲除lpa(1)或同时敲除lpa(1)和lpa(2)会导致50 - 65%的新生小鼠死亡,但存活者没有明显的皮层表型,这表明存在补偿性信号系统来调节皮层发育。一种功能获得模型,即通过外源性给予LPA增加受体激活来实现,结果表明LPA信号通过影响胚胎发育过程中的增殖、分化和细胞存活来调节大脑皮层的生长和结构。