Department of Molecular Biology, Helen L. Dorris Institute for Neurological and Psychiatric Disorders, The Scripps Research Institute, La Jolla, California 92037, USA.
Annu Rev Pharmacol Toxicol. 2010;50:157-86. doi: 10.1146/annurev.pharmtox.010909.105753.
Lysophosphatidic acid (LPA) is a small, ubiquitous phospholipid that acts as an extracellular signaling molecule by binding to and activating at least five known G protein-coupled receptors (GPCRs): LPA(1)-LPA(5). They are encoded by distinct genes named LPAR1-LPAR5 in humans and Lpar1-Lpar5 in mice. The biological roles of LPA are diverse and include developmental, physiological, and pathophysiological effects. This diversity is mediated by broad and overlapping expression patterns and multiple downstream signaling pathways activated by cognate LPA receptors. Studies using cloned receptors and genetic knockout mice have been instrumental in uncovering the significance of this signaling system, notably involving basic cellular processes as well as multiple organ systems such as the nervous system. This has further provided valuable proof-of-concept data to support LPA receptors and LPA metabolic enzymes as targets for the treatment of medically important diseases that include neuropsychiatric disorders, neuropathic pain, infertility, cardiovascular disease, inflammation, fibrosis, and cancer.
溶血磷脂酸(LPA)是一种小而普遍存在的磷脂,通过与至少五种已知的 G 蛋白偶联受体(GPCR)结合并激活它们来充当细胞外信号分子:LPA(1)-LPA(5)。它们由不同的基因编码,人类中命名为 LPAR1-LPAR5,小鼠中命名为 Lpar1-Lpar5。LPA 的生物学作用多种多样,包括发育、生理和病理生理作用。这种多样性是通过广泛和重叠的表达模式以及由同源 LPA 受体激活的多种下游信号通路介导的。使用克隆受体和基因敲除小鼠的研究在揭示该信号系统的重要性方面发挥了重要作用,特别是涉及基本细胞过程以及多个器官系统,如神经系统。这进一步提供了有价值的概念验证数据,支持 LPA 受体和 LPA 代谢酶作为治疗包括神经精神疾病、神经病理性疼痛、不育、心血管疾病、炎症、纤维化和癌症在内的重要医学疾病的靶点。