Publication | Open Access
LRP1 integrates murine macrophage cholesterol homeostasis and inflammatory responses in atherosclerosis
96
Citations
63
References
2017
Year
Knockin Mouse ModelImmunologyHyperlipidemiaCellular PhysiologyInflammationMetabolic SyndromeMetabolic SignalingCell SignalingAtherosclerosisDyslipidemiaLipid DisorderMolecular SignalingHealth SciencesMolecular PhysiologyChronic InflammationVascular BiologyLipid ScienceCell BiologyInflammatory ResponsesSignal TransductionPhysiologyEndothelial DysfunctionReverse Cholesterol TransportLipoprotein MetabolismCellular BiochemistryLdl ReceptorMedicineLipid Synthesis
Low-density lipoprotein receptor-related protein 1 (LRP1) is a multifunctional cell surface receptor with diverse physiological roles, ranging from cellular uptake of lipoproteins and other cargo by endocytosis to sensor of the extracellular environment and integrator of a wide range of signaling mechanisms. As a chylomicron remnant receptor, LRP1 controls systemic lipid metabolism in concert with the LDL receptor in the liver, whereas in smooth muscle cells (SMC) LRP1 functions as a co-receptor for TGFβ and PDGFRβ in reverse cholesterol transport and the maintenance of vascular wall integrity. Here we used a knockin mouse model to uncover a novel atheroprotective role for LRP1 in macrophages where tyrosine phosphorylation of an NPxY motif in its intracellular domain initiates a signaling cascade along an LRP1/SHC1/PI3K/AKT/PPARγ/LXR axis to regulate and integrate cellular cholesterol homeostasis through the expression of the major cholesterol exporter ABCA1 with apoptotic cell removal and inflammatory responses.
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