Female gene networks are expressed in myofibroblast-like smooth muscle cells in vulnerable atherosclerotic plaques

Author:

Benavente Ernest DiezORCID,Karnewar Santosh,Buono Michele,Mili EloiORCID,Hartman Robin J. G.,Kapteijn Daniek,Slenders LotteORCID,Daniels Mark,Aherrahrou RedouaneORCID,Reinberger TobiasORCID,Mol Barend M.,de Borst Gert J.ORCID,de Kleijn Dominique P. V.ORCID,Prange Koen H. M.ORCID,Depuydt Marie A. C.ORCID,de Winther Menno P. J.ORCID,Kuiper JohanORCID,Björkegren Johan L. M.ORCID,Erdmann JeanetteORCID,Civelek MeteORCID,Mokry MichalORCID,Owens Gary KORCID,Pasterkamp GerardORCID,den Ruijter Hester M.ORCID

Abstract

AbstractWomen presenting with coronary artery disease (CAD) more often present with fibrous atherosclerotic plaques, which are currently understudied. Phenotypically modulated smooth muscle cells (SMCs) contribute to atherosclerosis in women. How these phenotypically modulated SMCs shape female versus male plaques is unknown. Here, we show sex-stratified gene regulatory networks (GRNs) from human carotid atherosclerotic tissue. Prioritization of these networks identified two main SMC GRNs in late-stage atherosclerosis. Single-cell RNA-sequencing mapped these GRNs to two SMC phenotypes: a phenotypically modulated myofibroblast-like SMC network and a contractile SMC network. The myofibroblast-like GRN was mostly expressed in plaques that were vulnerable in females. Finally, mice orthologs of the female myofibroblast-like genes showed retained expression in advanced plaques from female mice but were downregulated in male mice during atherosclerosis progression. Female atherosclerosis is driven by GRNs that promote a fibrous vulnerable plaque rich in myofibroblast-like SMCs.

Publisher

Cold Spring Harbor Laboratory

Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Macrophage profiling in atherosclerosis: understanding the unstable plaque;Basic Research in Cardiology;2024-01-20

2. Phenotypic Switching of Vascular Smooth Muscle Cells in Atherosclerosis;Journal of the American Heart Association;2023-10-17

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