Mueller Paul, Ye Shaojing, Morris Andrew, Smyth Susan S
Division of Cardiovascular Medicine, The Gill Heart Institute, United States.
Division of Cardiovascular Medicine, The Gill Heart Institute, United States; Department of Veterans Affairs Medical Center Lexington, KY 40511, United States.
Exp Cell Res. 2015 May 1;333(2):190-194. doi: 10.1016/j.yexcr.2015.03.016. Epub 2015 Mar 28.
Acting through cell surface receptors, “extracellular” lysophosphatidic acid (LPA) influences cell growth, differentiation, apoptosis and development in a wide spectrum of settings [–5]. Within the vasculature, smooth muscle cells [6, 7], endothelial cells [8] and platelets [9, 10] display notable responses to LPA [11, 12], which likely regulate blood vessel development and contribute to vascular pathology. The bioactive effects of LPA are mediated by a family of G-protein coupled receptors with at least six members (termed LPA that are encoded by the genes in humans and in mice) [–3]. LPA may also serve as a ligand for the receptor for advanced glycation end products (RAGE) [13]. This review summarizes evidence to support a role for LPA signaling in vascular biology based on studies of LPA receptors and enzymes that produce or metabolize the lipid (Figure 1).
“细胞外”溶血磷脂酸(LPA)通过细胞表面受体发挥作用,在多种情况下影响细胞生长、分化、凋亡和发育[–5]。在脉管系统中,平滑肌细胞[6, 7]、内皮细胞[8]和血小板[9, 10]对LPA表现出显著反应[11, 12],这可能调节血管发育并导致血管病变。LPA的生物活性作用由一个G蛋白偶联受体家族介导,该家族至少有六个成员(在人类中由基因编码,在小鼠中由基因编码,称为LPA)[–3]。LPA还可能作为晚期糖基化终产物受体(RAGE)的配体[13]。本综述基于对LPA受体以及产生或代谢该脂质的酶的研究,总结了支持LPA信号在血管生物学中作用的证据(图1)。