Ye Xiaoqin, Fukushima Nobuyuki, Kingsbury Marcy A, Chun Jerold
Department of Pharmacology, School of Medicine, University of California, San Diego, La Jolla, CA 92093-0636, USA.
Neuroreport. 2002 Dec 3;13(17):2169-75. doi: 10.1097/00001756-200212030-00002.
The physiological and pathological importance of lysophosphatidic acid (LPA) in the nervous system is underscored by its presence, as well as the expression of its receptors in neural tissues. In fact, LPA produces responses in a broad range of cell types related to the function of the nervous system. These cell types include neural cell lines, neural progenitors, primary neurons, oligodendrocytes, Schwann cells, astrocytes, microglia, and brain endothelial cells. LPA-induced cell type-specific effects include changes in cell morphology, promotion of cell proliferation and cell survival, induction of cell death, changes in ion conductance and Ca2+ mobilization, induction of pain transmission, and stimulation of vasoconstriction. These effects are mediated through a number of G protein-coupled LPA receptors that activate various downstream signaling cascades. This review provides a current summary of LPA-induced effects in neural cells in vitro or in vivo in combination with our current understanding of the signaling pathways responsible for these effects.
溶血磷脂酸(LPA)在神经组织中的存在及其受体的表达,凸显了其在神经系统中的生理和病理重要性。事实上,LPA在与神经系统功能相关的广泛细胞类型中产生反应。这些细胞类型包括神经细胞系、神经祖细胞、原代神经元、少突胶质细胞、施万细胞、星形胶质细胞、小胶质细胞和脑内皮细胞。LPA诱导的细胞类型特异性效应包括细胞形态变化、促进细胞增殖和细胞存活、诱导细胞死亡、离子电导和Ca2+动员变化、诱导疼痛传递以及刺激血管收缩。这些效应是通过一些激活各种下游信号级联反应的G蛋白偶联LPA受体介导的。本综述结合我们目前对负责这些效应的信号通路的理解,对LPA在体外或体内神经细胞中诱导的效应进行了当前总结。