Ren H, Panchatcharam M, Mueller P, Escalante-Alcalde D, Morris A J, Smyth S S
The Gill Heart Institute, Division of Cardiovascular Medicine, Lexington, KY 40536-0200, USA.
Biochim Biophys Acta. 2013 Jan;1831(1):126-32. doi: 10.1016/j.bbalip.2012.07.012. Epub 2012 Jul 24.
Lipid phosphate phosphatases (LPP) are integral membrane proteins with broad substrate specificity that dephosphorylate lipid substrates including phosphatidic acid, lysophosphatidic acid, ceramide 1-phosphate, sphingosine 1-phosphate, and diacylglycerol pyrophosphate. Although the three mammalian enzymes (LPP1-3) demonstrate overlapping catalytic activities and substrate preferences in vitro, the phenotypes of mice with targeted inactivation of the Ppap2 genes encoding the LPP enzymes reveal nonredundant functions. A specific role for LPP3 in vascular development has emerged from studies of mice lacking Ppap2b. A meta-analysis of multiple, large genome-wide association studies identified a single nucleotide polymorphism in PPAP2B as a novel predictor of coronary artery disease. In this review, we will discuss the evidence that links LPP3 to vascular development and disease and evaluate potential molecular mechanisms. This article is part of a Special Issue entitled Advances in Lysophospholipid Research.
脂质磷酸磷酸酶(LPP)是具有广泛底物特异性的整合膜蛋白,可使脂质底物去磷酸化,这些底物包括磷脂酸、溶血磷脂酸、1-磷酸神经酰胺、1-磷酸鞘氨醇和二磷酸二酰甘油。尽管三种哺乳动物酶(LPP1-3)在体外表现出重叠的催化活性和底物偏好,但编码LPP酶的Ppap2基因靶向失活的小鼠的表型显示出非冗余功能。对缺乏Ppap2b的小鼠的研究揭示了LPP3在血管发育中的特定作用。对多项大型全基因组关联研究的荟萃分析确定,PPAP2B中的一个单核苷酸多态性是冠状动脉疾病的一种新的预测指标。在这篇综述中,我们将讨论将LPP3与血管发育和疾病联系起来的证据,并评估潜在的分子机制。本文是名为《溶血磷脂研究进展》的特刊的一部分。