Increased atherosclerosis in mice reconstituted with apolipoprotein E null macrophages

Macrophage-derived foam cells express apolipoprotein E (apoE) abundantly in atherosclerotic lesions. To examine the physiologic role of apoE secretion by the macrophage in atherogenesis, bone marrow transplantation was used to reconstitute C57BL/6 mice with macrophages that were either null or wild...

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Veröffentlicht in:Proceedings of the National Academy of Sciences - PNAS 1997-04, Vol.94 (9), p.4647-4652
Hauptverfasser: Fazio, S. (Vanderbilt University School of Medicine, Nashville, TN.), Babaev, V.R, Murray, A.B, Hasty, A.H, Carter, K.J, Gleaves, L.A, Atkinson, J.B, Linton, M.F
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Sprache:eng
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Zusammenfassung:Macrophage-derived foam cells express apolipoprotein E (apoE) abundantly in atherosclerotic lesions. To examine the physiologic role of apoE secretion by the macrophage in atherogenesis, bone marrow transplantation was used to reconstitute C57BL/6 mice with macrophages that were either null or wild type for the apoE gene. After 13 weeks on an atherogenic diet, C57BL/6 mice reconstituted with apoE null marrow developed 10-fold more atherosclerosis than controls in the absence of significant differences in serum cholesterol levels or lipoprotein profiles. ApoE expression was absent in the macrophage-derived foam cells of C57BL/6 mice reconstituted with apoE null marrow. Thus, lack of apoE expression by the macrophage promotes foam cell formation. These data support a protective role for apoE expression by the macrophage in early atherogenesis
ISSN:0027-8424
1091-6490
DOI:10.1073/pnas.94.9.4647