Ishii Isao, Fukushima Nobuyuki, Ye Xiaoqin, Chun Jerold
Department of Molecular Genetics, National Institute of Neuroscience, NCNP, Kodaira, Tokyo 187-8502, Japan.
Annu Rev Biochem. 2004;73:321-54. doi: 10.1146/annurev.biochem.73.011303.073731.
Lysophospholipids (LPs), such as lysophosphatidic acid and sphingosine 1-phosphate, are membrane-derived bioactive lipid mediators. LPs can affect fundamental cellular functions, which include proliferation, differentiation, survival, migration, adhesion, invasion, and morphogenesis. These functions influence many biological processes that include neurogenesis, angiogenesis, wound healing, immunity, and carcinogenesis. In recent years, identification of multiple cognate G protein-coupled receptors has provided a mechanistic framework for understanding how LPs play such diverse roles. Generation of LP receptor-null animals has allowed rigorous examination of receptor-mediated physiological functions in vivo and has identified new functions for LP receptor signaling. Efforts to develop LP receptor subtype-specific agonists/antagonists are in progress and raise expectations for a growing collection of chemical tools and potential therapeutic compounds. The rapidly expanding literature on the LP receptors is herein reviewed.
溶血磷脂(LPs),如溶血磷脂酸和1-磷酸鞘氨醇,是膜衍生的生物活性脂质介质。LPs可影响细胞的基本功能,包括增殖、分化、存活、迁移、黏附、侵袭和形态发生。这些功能影响许多生物学过程,包括神经发生、血管生成、伤口愈合、免疫和致癌作用。近年来,多种同源G蛋白偶联受体的鉴定为理解LPs如何发挥如此多样的作用提供了一个机制框架。LP受体基因敲除动物的产生使得在体内对受体介导的生理功能进行严格研究成为可能,并确定了LP受体信号传导的新功能。开发LP受体亚型特异性激动剂/拮抗剂的工作正在进行中,这增加了人们对越来越多的化学工具和潜在治疗化合物的期待。本文综述了关于LP受体的迅速增长的文献。