Immunometabolism orchestrates training of innate immunity in atherosclerosis.

Abstract:

:Atherosclerosis is characterized by a persistent, low-grade inflammation of the arterial wall. Monocytes and monocyte-derived macrophages play a pivotal role in the various stages of atherosclerosis. In the past few years, metabolic reprogramming has been identified as an important controller of myeloid cell activation status. In addition, metabolic and epigenetic reprogramming are key regulatory mechanisms of trained immunity, which denotes the non-specific innate immune memory that can develop after brief stimulation of monocytes with microbial or non-microbial stimuli. In this review, we build the case that metabolic reprogramming of monocytes and macrophages, and trained immunity in particular, contribute to the pathophysiology of atherosclerosis. We discuss the specific metabolic adaptations, including changes in glycolysis, oxidative phosphorylation, and cholesterol metabolism, that have been reported in atherogenic milieus in vitro and in vivo. In addition, we will focus on the role of these metabolic pathways in the development of trained immunity.

journal_name

Cardiovasc Res

journal_title

Cardiovascular research

authors

van Tuijl J,Joosten LAB,Netea MG,Bekkering S,Riksen NP

doi

10.1093/cvr/cvz107

subject

Has Abstract

pub_date

2019-07-01 00:00:00

pages

1416-1424

issue

9

eissn

0008-6363

issn

1755-3245

pii

5485242

journal_volume

115

pub_type

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