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Atherosclerosis in Different Vascular Locations Unbiasedly Approached with Mouse Genetics.

Abstract
Atherosclerosis in different vascular locations leads to distinct clinical consequences, such as ischemic stroke and myocardial infarction. Genome-wide association studies in humans revealed that genetic loci responsible for carotid plaque and coronary artery disease were not overlapping, suggesting that distinct genetic pathways might be involved for each location. While elevated plasma cholesterol is a common risk factor, plaque development in different vascular beds is influenced by hemodynamics and intrinsic vascular integrity. Despite the limitation of species differences, mouse models provide platforms for unbiased genetic approaches. Mouse strain differences also indicate that susceptibility to atherosclerosis varies, depending on vascular locations, and that the location specificity is genetically controlled. Quantitative trait loci analyses in mice suggested candidate genes, including Mertk and Stab2, although how each gene affects the location-specific atherosclerosis needs further elucidation. Another unbiased approach of single-cell transcriptome analyses revealed the presence of a small subpopulation of vascular smooth muscle cells (VSMCs), which are "hyper-responsive" to inflammatory stimuli. These cells are likely the previously-reported Sca1+ progenitor cells, which can differentiate into multiple lineages in plaques. Further spatiotemporal analyses of the progenitor cells are necessary, since their distribution pattern might be associated with the location-dependent plaque development.
AuthorsYukako Kayashima, Nobuyo Maeda-Smithies
JournalGenes (Genes (Basel)) Vol. 11 Issue 12 (11 28 2020) ISSN: 2073-4425 [Electronic] Switzerland
PMID33260687 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Review)
Topics
  • Animals
  • Atherosclerosis (genetics, metabolism)
  • Cell Adhesion (genetics)
  • Genome-Wide Association Study
  • Mice
  • Muscle, Smooth, Vascular (metabolism)
  • Myocytes, Smooth Muscle (metabolism)
  • Plaque, Atherosclerotic (genetics, metabolism)

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