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引用次数: 81
摘要
溶血磷脂(LPs),如溶血磷脂酸(LPA)和鞘氨醇-1-磷酸(S1P)是定量的次要磷脂物种,但仍能作为细胞外信号。作为一个由脂质主导的器官系统,神经系统似乎可能是这种细胞间信号传递形式的受益者。然而,确定这些脂质的神经生物学重要性的一个主要困难是缺乏克隆受体。由于缺乏特异性的、竞争性的拮抗剂来阻断功能,这些受体的不可获得性、不确定的存在性尤其成问题。此外,这些脂类具有类似洗涤剂的化学结构,这就提出了一种解释,即外源性溶血磷脂的任何观察到的作用都可能是由于非特异性的膜扰动。在研究与大脑皮层神经发生相关的g蛋白偶联受体(GPCR)基因时,分离到了第一个溶血磷脂受体基因(lpA1/vzg-1) (Hecht et al., J. Cell Biol.)。, 135,1071, 1996),暗示受体介导的溶血磷脂信号是神经系统发育和功能的潜在重要组成部分。表达研究表明在神经发生、皮层发育和对胶质细胞,特别是少突胶质细胞和雪旺细胞发育的影响中起作用。本文综述了LP受体的分子生物学,细胞内信号传导的相关方面,以及它们在神经系统中的可能作用。
Lysophospholipid receptors: implications for neural signaling.
Lysophospholipids (LPs) such as lysophosphatidic acid (LPA) and sphingosine-1-phosphate (S1P) represent quantitatively minor phospholipid species that nonetheless are capable of acting as extracellular signals. As an organ system dominated by lipids, the nervous system would seem a likely benefactor of this form of intercellular signaling. A major difficulty in determining the neurobiological importance of these lipids, however, has been a lack of cloned receptors. The unavailability, indeed, uncertain existence, of these receptors has been particularly problematic because of the absence of specific, competitive antagonists to block function. Further, these lipids have detergent-like chemical structures, raising the explanation that any observed effects of exogenously applied lysophospholipids could be due to nonspecific membrane perturbations. During studies of G-protein coupled receptor (GPCR) genes involved with cerebral cortical neurogenesis, the first lysophospholipid receptor gene (lpA1/vzg-1) was isolated (Hecht et al., J. Cell Biol., 135, 1071, 1996), implicating receptor-mediated lysophospholipid signaling as potentially important components of nervous system development and function. Expression studies indicated roles in neurogenesis, cortical development, and effects on glia, particularly oligodendrocyte and Schwann cell development. Reviewed here are the molecular biology of LP receptors, relevant aspects of intracellular signaling, and their possible roles in the nervous system.