Benavente Ernest Diez, Karnewar Santosh, Buono Michele, Mili Eloi, Hartman Robin J G, Kapteijn Daniek, Slenders Lotte, Daniels Mark, Aherrahrou Redouane, Reinberger Tobias, Mol Barend M, de Borst Gert J, de Kleijn Dominique P V, Prange Koen H M, Depuydt Marie A C, de Winther Menno P J, Kuiper Johan, Björkegren Johan L M, Erdmann Jeanette, Civelek Mete, Mokry Michal, Owens Gary K, Pasterkamp Gerard, den Ruijter Hester M
Laboratory of Experimental Cardiology, University Medical Center Utrecht, Utrecht University, the Netherlands.
Robert M. Berne Cardiovascular Research Center, University of Virginia, Charlottesville, VA, USA.
bioRxiv. 2023 Feb 9:2023.02.08.527690. doi: 10.1101/2023.02.08.527690.
Women 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.
患有冠状动脉疾病(CAD)的女性更常出现纤维性动脉粥样硬化斑块,目前对此研究不足。表型调节的平滑肌细胞(SMC)在女性动脉粥样硬化中起作用。这些表型调节的SMC如何塑造女性与男性的斑块尚不清楚。在这里,我们展示了来自人类颈动脉粥样硬化组织的性别分层基因调控网络(GRN)。对这些网络进行优先级排序后,在晚期动脉粥样硬化中确定了两个主要的SMC GRN。单细胞RNA测序将这些GRN映射到两种SMC表型:一种表型调节的成肌纤维细胞样SMC网络和一种收缩性SMC网络。成肌纤维细胞样GRN主要在女性易损斑块中表达。最后,雌性成肌纤维细胞样基因的小鼠直系同源基因在雌性小鼠的晚期斑块中仍保留表达,但在雄性小鼠动脉粥样硬化进展过程中被下调。女性动脉粥样硬化由促进富含成肌纤维细胞样SMC的纤维性易损斑块的GRN驱动。