Year: 2026
Type: preprint
Abstract: Genetic variants in the Cerebral Cavernous Malformation 2 ( CCM2 ) locus are associated with coronary artery disease (CAD), but the role of CCM2 in atherosclerosis is unknown. We previously identified CCM2 through endothelial cell (EC) Perturb-seq as a regulator of transcriptional programs enriched for CAD risk genes, and predicted that reduced CCM2 function would be athero-protective. Here, we integrated human genetics, functional studies in human aortic ECs, and single cell profiling with mouse models of atherosclerosis to define the effects of reduced CCM2 signaling across disease stages. Ccm2 +/- mice developed less atherosclerosis after 12 weeks of high-fat, high-cholesterol diet. At baseline, aortic ECs from Ccm2 +/- mice exhibited reduced inflammatory transcriptional programs, and CCM2 knockout in human aortic ECs increased KLF2 expression and reduced monocyte adhesion and procoagulant activity. However, this protective phenotype was not sustained during disease progression. After 12 weeks of high-fat, high-cholesterol diet, Ccm2 +/- mice exhibited increased circulating TNFα and increased inflammatory programs in aortic ECs and T cells. Consistent with this transition, Ccm2 +/- showed increased atherosclerotic burden after 20 weeks of atherogenic diet. Human genetic analyses showed a similar context-dependent association. The lead variant in the CCM2 locus (rs2107732, a missense V53I coding variant in CCM2 ) was associated with lower CAD risk in the general population but higher CAD risk in clinical trial cohorts enriched for cardiometabolic disease. These results demonstrate how the phenotypic consequences of a CAD-associated gene can depend on disease context and stage. One Sentence Summary CCM2 heterozygosity reduces endothelial inflammation and early atherosclerosis but worsens late-stage disease, consistent with human genetics.
Source: medRxiv
Authors: Shi Fang, Gavin R. Schnitzler, Amélie Vromman, Jiahao Jiang, Mohita Maurya, Frederick K. Kamanu, James J Park, Ran Cui, Ronodeep Mitra, Allison Gabbert, Cindy Zheng, Lily Widdup, Jathin S. Rao, Natalie Pham, Mengyu Chen, Seid Miad Zandavi, Jesse M. Engreitz, Martin S. Taylor, Nicholas A. Marston, Alec A. Schmaier, Marc S. Sabatine, Peter Libby, Christian T. Ruff, Rajat M. Gupta
Language: English
Subfield: Immunology
Field: Immunology and Microbiology
Domain: Life Sciences
Open Access status: green
Awards: G3548749230, G5211151649, A genetic approach to identify the common mechanisms of vascular disease, High-throughput cellular genetics to connect noncoding variants to coronary artery disease genes, Mapping, modeling, and manipulating 3D contacts in vascular cells to connect risk variants to disease genes, Identifying causal gene programs for vascular disease using high throughput CRISPR genomics, Regulation of endothelial cell phosphatidylserine in thrombosis
OpenAlex ID: W7224825319