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Lipid phosphate phosphatase (LPP3) and vascular development
Authors:H. Ren  M. Panchatcharam  P. Mueller  D. Escalante-Alcalde  A.J. Morris  S.S. Smyth
Affiliation:1. The Gill Heart Institute, Division of Cardiovascular Medicine, 900 S. Limestone, Lexington, KY 40536‐0200, USA;2. División de Neurociencias, Instituto de Fisiología Celular, Universidad Nacional Autónoma de México, Ciudad Universitaria, 04510, Mexico;3. Veterans Affairs Medical Center, Lexington, KY, USA
Abstract: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.
Keywords:Lysophospholipid   Vascular development   Sphingosine-1-phosphate   Lysophosphatidic acid   Endothelial cell
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