Kabarowski Janusz H S, Xu Yan, Witte Owen N
Department of Microbiology, Immunology & Molecular Genetics, University of California-Los Angeles, 5-748 MRL, 675 Charles E. Young Drive South, Box 951662, Los Angeles, CA 90095-1662, USA.
Biochem Pharmacol. 2002 Jul 15;64(2):161-7. doi: 10.1016/s0006-2952(02)01179-6.
Despite the recognized effects of lysophosphatidylcholine upon cells of the immune system and its association with inflammatory processes, its mechanism of action has remained poorly characterized. Our recent identification of the first lysophosphatidylcholine receptor as an immunoregulatory G protein-coupled receptor named G2A whose genetic ablation results in the development of inflammatory autoimmune disease has, therefore, provided a new perspective on the role of this lysophospholipid as a modulator of immune responses. This commentary discusses the biological properties of lysophosphatidylcholine as an immunoregulatory ligand for cells of the innate and adaptive arms of the immune system. Although we focus primarily on ligand interactions with G2A, we also discuss the issue of possible functional redundancy with other receptors with recently established ligand specificities towards phosphorylcholine-containing lysolipids including lysophosphatidylcholine.
尽管溶血磷脂酰胆碱对免疫系统细胞具有公认的作用,且与炎症过程相关,但其作用机制仍未得到充分阐明。因此,我们最近鉴定出首个溶血磷脂酰胆碱受体是一种名为G2A的免疫调节G蛋白偶联受体,其基因敲除会导致炎症性自身免疫疾病的发生,这为这种溶血磷脂作为免疫反应调节剂的作用提供了新的视角。本评论讨论了溶血磷脂酰胆碱作为免疫系统先天性和适应性分支细胞的免疫调节配体的生物学特性。虽然我们主要关注配体与G2A的相互作用,但我们也讨论了与其他对含磷酰胆碱的溶血脂质(包括溶血磷脂酰胆碱)具有最近确定的配体特异性的受体可能存在功能冗余的问题。