Toda Akiko, Yokomizo Takehiko, Shimizu Takao
Department of Biochemistry and Molecular Biology, Faculty of Medicine, The University of Tokyo, Japan.
Prostaglandins Other Lipid Mediat. 2002 Aug;68-69:575-85. doi: 10.1016/s0090-6980(02)00056-4.
Leukotriene B4 (LTB4) is a potent chemotactic agent and activating factor for granulocytes. Two cell surface receptors for LTB4 (BLT1 and BLT2) have been isolated in the last few years. These receptors are G-protein-coupled receptors (GPCR), and they have 45% amino acid identity. BLT1 and BLT2 are high- and low- affinity receptors, respectively. Cells transfected with BLT1 and BLT2 show LTB4-dependent intracellular signal transduction and chemotaxis in vitro. The distribution and pharmacological characteristics of BLT1 and BLT2 are different, suggesting distinct roles for these receptors in vivo. The open reading frame (ORF) of BLT2 overlaps the promoter of BLT1, a so called 'promoter in ORF'. Based on recent publications on BLT1 transgenic and knock out mice phenotypes, it appears that LTB4 plays important roles in inflammation in addition to host defense in vivo.
白三烯B4(LTB4)是一种对粒细胞具有强大趋化作用的趋化剂和激活因子。在过去几年中,已分离出两种LTB4的细胞表面受体(BLT1和BLT2)。这些受体是G蛋白偶联受体(GPCR),它们具有45%的氨基酸同一性。BLT1和BLT2分别是高亲和力和低亲和力受体。用BLT1和BLT2转染的细胞在体外显示出LTB4依赖性细胞内信号转导和趋化作用。BLT1和BLT2的分布及药理学特性不同,表明这些受体在体内具有不同的作用。BLT2的开放阅读框(ORF)与BLT1的启动子重叠,即所谓的“ORF中的启动子”。基于最近关于BLT1转基因和基因敲除小鼠表型的出版物,似乎LTB4在体内除了宿主防御外,在炎症中也起着重要作用。