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Liver X receptor activation stimulates iron export in human alternative macrophages.

Abstract : RATIONALE: In atherosclerotic plaques, iron preferentially accumulates in macrophages where it can exert pro-oxidant activities. OBJECTIVE: The objective of this study was, first, to better characterize the iron distribution and metabolism in macrophage subpopulations in human atherosclerotic plaques and, second, to determine whether iron homeostasis is under the control of nuclear receptors, such as the liver X receptors (LXRs). METHODS AND RESULTS: Here we report that iron depots accumulate in human atherosclerotic plaque areas enriched in CD68 and mannose receptor (MR)-positive (CD68(+)MR(+)) alternative M2 macrophages. In vitro IL-4 polarization of human monocytes into M2 macrophages also resulted in a gene expression profile and phenotype favoring iron accumulation. However, M2 macrophages on iron exposure acquire a phenotype favoring iron release, through a strong increase in ferroportin expression, illustrated by a more avid oxidation of extracellular low-density lipoprotein by iron-loaded M2 macrophages. In line, in human atherosclerotic plaques, CD68(+)MR(+) macrophages accumulate oxidized lipids, which activate LXRα and LXRβ, resulting in the induction of ABCA1, ABCG1, and apolipoprotein E expression. Moreover, in iron-loaded M2 macrophages, LXR activation induces nuclear factor erythroid 2-like 2 expression, thereby increasing ferroportin expression, which, together with a decrease of hepcidin mRNA levels, promotes iron export. CONCLUSIONS: These data identify a role for M2 macrophages in iron handling, a process regulated by LXR activation.
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Contributor : Marie-Hélène Derudas Connect in order to contact the contributor
Submitted on : Friday, March 14, 2014 - 11:20:31 AM
Last modification on : Wednesday, March 23, 2022 - 3:51:03 PM
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Gael Bories, Sophie Colin, Jonathan Vanhoutte, Bruno Derudas, Corinne Copin, et al.. Liver X receptor activation stimulates iron export in human alternative macrophages.. Circulation Research, American Heart Association, 2013, 113 (11), pp.1196-205. ⟨10.1161/CIRCRESAHA.113.301656⟩. ⟨inserm-00870992⟩



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