LRP1 integrates murine macrophage cholesterol homeostasis and inflammatory responses in atherosclerosis

Author:

Xian Xunde1ORCID,Ding Yinyuan12ORCID,Dieckmann Marco1,Zhou Li1,Plattner Florian34ORCID,Liu Mingxia5,Parks John S5ORCID,Hammer Robert E6,Boucher Philippe7,Tsai Shirling89,Herz Joachim141011ORCID

Affiliation:

1. Departments of Molecular Genetics, UT Southwestern Medical Center, Dallas, United States

2. Key Laboratory of Medical Electrophysiology, Ministry of Education of China, Institute of Cardiovascular Research, Southwest Medical University, Luzhou, China

3. Department of Psychiatry, University of Texas Southwestern Medical Center, Dallas, United States

4. Center for Translational Neurodegeneration Research, University of Texas Southwestern Medical Center, Dallas, United States

5. Section on Molecular Medicine, Department of Internal Medicine, Wake Forest School of Medicine, Winston-Salem, North Carolina

6. Department of Biochemistry, University of Texas Southwestern Medical Center, Dallas, United States

7. CNRS, UMR 7213, University of Strasbourg, Illkirch, France

8. Department of Surgery, UT Southwestern Medical Center, Dallas, United States

9. Dallas VA Medical Center, Dallas, United States

10. Department of Neuroscience, UT Southwestern, Dallas, United States

11. Department of Neurology and Neurotherapeutics, UT Southwestern, Dallas, United States

Abstract

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.

Funder

National Institutes of Health

Fondation de France

Fondation pour la Recherche Médicale

Agence Nationale de la Recherche

North Texas Veterans Affairs Health Care Systems

American Surgical Association Foundation

Consortium for Frontotemporal Dementia Research

Bright Focus Foundation

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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