Deficiency of adipose differentiation-related protein impairs foam cell formation and protects against atherosclerosis
Open accessAbstract
Foam cells are a hallmark of atherosclerosis. However, it is unclear whether foam cell formation per se protects against atherosclerosis or fuels it. In this study, we investigated the role of adipose differentiation-related protein (ADFP), a major lipid droplet protein (LDP), in the regulation of foam cell formation and atherosclerosis. We show that ADFP expression facilitates foam cell formation induced by modified lipoproteins in mouse macrophages in vitro. We show further that Adfp gene inactivation in apolipoprotein E-deficient (ApoE(-/-)) mice reduces the number of lipid droplets in foam cells in atherosclerotic lesions and protects the mice against atherosclerosis. Moreover, transplantation of ADFP-null bone marrow-derived cells effectively attenuated atherosclerosis in ApoE(-/-) mice. Deficiency of ADFP did not cause a detectable compensatory increase in the other PAT domain proteins in macrophages in vitro or in vivo. Mechanistically, ADFP enables the macrophage to maintain its lipid content by hindering lipid efflux. We detected no significant difference in lesion composition or in multiple parameters of inflammation in macrophages or in their phagocytic activity between mice with and without ADFP. In conclusion, Adfp inactivation in ApoE(-/-) background protects against atherosclerosis and appears to be a relatively pure model of impaired foam cell formation.
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PLIN2 is involved in the import and storage of cholesterol and fatty acids.
“PLIN2 has been shown to be involved in the import and storage of cholesterol and fatty acids (Paul et al., 2008).”
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Brown, M. S., Ho, Y. K., & Goldstein, J. L. (1980) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)70568-7 · Cited by 722 · see citing works
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Schubert, M., Becher, S., Wallert, M., Maeß, M. B., Abhari, M., Rennert, K., Mosig, A. S., Große, S., Heller, R., Grün, M., et al. (2020) · Molecular Pharmacology · doi:10.1124/mol.119.117887 · Cited by 35 · see citing works
- Authors
- Paul, A., Chang, B. H.-J., Li, L., Yechoor, V. K., & Chan, L.
- Affiliations
- Baylor College of Medicine (US)
- Venue
- Circulation Research
- Published
- 2008-06-20
- Volume
- 102
- Issue
- 12
- Pages
- 1492-1501
- ISSN
- 0009-7330 (ISSN-L)
- 1524-4571
- PMC
- PMC2773502
- OpenAlex
- W2147593845
- Cited by
- 171
- References
- 1
- Citations by year
- 2026: 7 · 2025: 8 · 2024: 9 · 2023: 14 · 2022: 11 · 2021: 9 · 2020: 9 · 2019: 8 · 2018: 12 · 2017: 12 · 2016: 8 · 2015: 10 · 2014: 4 · 2013: 13 · 2012: 9
- FWCI
- 3.91
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Circulation Research (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Heart, Lung, and Blood Institute (HL-51586, R01HL051586)
- National Institute of Diabetes and Digestive and Kidney Diseases (P30DK-56338, P30DK056338)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Atherosclerosis and Cardiovascular Diseases
- Health Sciences › Medicine › Surgery › Cholesterol and Lipid Metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Lipid metabolism and biosynthesis
- Keywords
- ADRP, foam cell formation, atherosclerosis, lipid droplets, macrophages, lipid efflux, modified lipoproteins, ApoE-deficient mice, bone marrow transplantation, atherosclerotic plaque composition
- MeSH terms
- Perilipin-2, Perilipin-3, Animals, Aorta, Aortic Diseases, Apolipoproteins E, Biological Transport, Carrier Proteins, Cells, Cultured, Cholesterol, Female, Fibroblasts, Foam Cells, Lipoproteins, LDL, Male, Membrane Proteins, Mice, Inbred C57BL, RNA, Messenger, Protein Structure, Tertiary, Macrophages, Peritoneal, CD36 Antigens, Atherosclerosis, Lipid Metabolism, Scavenger Receptors, Class A, Mice
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