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Anti-Inflammatory Effects of HDL (High-Density Lipoprotein) in Macrophages Predominate Over Proinflammatory Effects in Atherosclerotic Plaques.

Citation
Fotakis, P., et al. “Anti-Inflammatory Effects Of Hdl (High-Density Lipoprotein) In Macrophages Predominate Over Proinflammatory Effects In Atherosclerotic Plaques.”. Arteriosclerosis, Thrombosis, And Vascular Biology, pp. e253-e272.
Center University of Washington
Author Panagiotis Fotakis, Vishal Kothari, David G Thomas, Marit Westerterp, Matthew M Molusky, Elissa Altin, Sandra Abramowicz, Nan Wang, Yi He, Jay W Heinecke, Karin E Bornfeldt, Alan R Tall
Keywords cholesterol, High-density lipoprotein, inflammation, macrophages, rHDL infusion
Abstract

OBJECTIVE: HDL (high-density lipoprotein) infusion reduces atherosclerosis in animal models and is being evaluated as a treatment in humans. Studies have shown either anti- or proinflammatory effects of HDL in macrophages, and there is no consensus on the underlying mechanisms. Here, we interrogate the effects of HDL on inflammatory gene expression in macrophages. Approach and Results: We cultured bone marrow-derived macrophages, treated them with reconstituted HDL or HDL isolated from mice, and challenged them with lipopolysaccharide. Transcriptional profiling showed that HDL exerts a broad anti-inflammatory effect on lipopolysaccharide-induced genes and proinflammatory effect in a subset of genes enriched for chemokines. Cholesterol removal by POPC (1-palmitoyl-2-oleoyl-glycero-3-phosphocholine) liposomes or β-methylcyclodextrin mimicked both pro- and anti-inflammatory effects of HDL, whereas cholesterol loading by POPC/cholesterol-liposomes or acetylated LDL (low-density lipoprotein) before HDL attenuated these effects, indicating that these responses are mediated by cholesterol efflux. While early anti-inflammatory effects reflect reduced TLR (Toll-like receptor) 4 levels, late anti-inflammatory effects are due to reduced IFN (interferon) receptor signaling. Proinflammatory effects occur late and represent a modified endoplasmic reticulum stress response, mediated by IRE1a (inositol-requiring enzyme 1a)/ASK1 (apoptosis signal-regulating kinase 1)/p38 MAPK (p38 mitogen-activated protein kinase) signaling, that occurs under conditions of extreme cholesterol depletion. To investigate the effects of HDL on inflammatory gene expression in myeloid cells in atherosclerotic lesions, we injected reconstituted HDL into or mice fed a Western-type diet. Reconstituted HDL infusions produced anti-inflammatory effects in lesion macrophages without any evidence of proinflammatory effects.

CONCLUSIONS: Reconstituted HDL infusions in hypercholesterolemic atherosclerotic mice produced anti-inflammatory effects in lesion macrophages suggesting a beneficial therapeutic effect of HDL in vivo.

Year of Publication
2019
Journal
Arteriosclerosis, thrombosis, and vascular biology
Volume
39
Issue
12
Number of Pages
e253-e272
Date Published
12/2019
ISSN Number
1524-4636
DOI
10.1161/ATVBAHA.119.313253
Alternate Journal
Arterioscler. Thromb. Vasc. Biol.
PMID
31578081
PMCID
PMC6879856
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