HDL promotes rapid atherosclerosis regression in mice and alters inflammatory properties of plaque monocyte-derived cells

Jonathan E. Feig, James X. Rong, Raanan Shamir, Marie Sanson, Yuliya Vengrenyuk, Jianhua Liu, Katey Rayner, Kathryn Moore, Michael Garabedian, Edward A. Fisher

Research output: Contribution to journalArticlepeer-review

Abstract

HDL cholesterol (HDL-C) plasma levels are inversely related to cardiovascular disease risk. Previous studies have shown in animals and humans that HDL promotes regression of atherosclerosis. We hypothesized that this was related to an ability to promote the loss of monocyte-derived cells (CD68 +, primarily macrophages and macrophage foam cells) from plaques. To test this hypothesis, we used an established model of atherosclerosis regression in which plaquebearing aortic arches from apolipoprotein E-deficient (apoE -/-) mice (low HDL-C, high non-HDL-C) were transplanted into recipient mice with differing levels of HDL-C and non-HDL-C: C57BL6 mice (normal HDL-C, low non-HDL-C), apoAI-/- mice (low HDL-C, low non-HDL-C), or apoE-/- mice transgenic for human apoAI (hAI/ apoE-/-; normal HDL-C, high non-HDL-C). Remarkably, despite persistent elevated non-HDL-C in hAI/apoE-/- recipients, plaque CD68+ cell content decreased by > 50% by 1 wk after transplantation, whereas there was little change in apoAI-/- recipient mice despite hypolipidemia. The decreased content of plaque CD68+ cells after HDL-C normalization was associated with their emigration and induction of their chemokine receptor CCR7. Furthermore, in CD68+ cells laser-captured from the plaques, normalization of HDLC led to decreased expression of inflammatory factors and enrichment of markers of the M2 (tissue repair) macrophage state. Again, none of these beneficial changes were observed in the apoAI-/-recipients, suggesting a major requirement for reverse cholesterol transport for the beneficial effects of HDL. Overall, these results establish HDL as a regulator in vivo of the migratory and inflammatory properties of monocyte-derived cells in mouse atherosclerotic plaques, and highlight the phenotypic plasticity of these cells.

Original languageEnglish
Pages (from-to)7166-7171
Number of pages6
JournalProceedings of the National Academy of Sciences of the United States of America
Volume108
Issue number17
DOIs
StatePublished - 26 Apr 2011
Externally publishedYes

Keywords

  • Alternative activation
  • Arginase I

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