Heterogeneity of immune cells in human atherosclerosis revealed by scRNA-Seq

Cardiovasc Res. 2021 Nov 22;117(13):2537-2543. doi: 10.1093/cvr/cvab260.

Abstract

Immune cells in atherosclerosis include T, B, natural killer (NK) and NKT cells, macrophages, monocytes, dendritic cells (DCs), neutrophils, and mast cells. Advances in single-cell RNA sequencing (sRNA-Seq) have refined our understanding of immune cell subsets. Four recent studies have used scRNA-Seq of immune cells in human atherosclerotic lesions and peripheral blood mononuclear cells (PBMCs), some including cell surface phenotypes revealed by oligonucleotide-tagged antibodies, which confirmed known and identified new immune cell subsets and identified genes significantly up-regulated in PBMCs from HIV+ subjects with atherosclerosis compared to PBMCs from matched HIV+ subjects without atherosclerosis. The ability of scRNA-Seq to identify cell types is greatly augmented by adding cell surface phenotype using antibody sequencing. In this review, we summarize the latest data obtained by scRNA-Seq on plaques and human PBMCs in human subjects with atherosclerosis.

Keywords: Antibodies; Atherosclerosis; Human; Transcriptomes; scRNA-Seq.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Atherosclerosis / genetics*
  • Atherosclerosis / immunology
  • Atherosclerosis / metabolism
  • Atherosclerosis / pathology
  • Gene Expression Profiling*
  • Genetic Heterogeneity*
  • Humans
  • Immune System / immunology*
  • Immune System / metabolism
  • Immune System / pathology
  • Immunophenotyping
  • Leukocytes / immunology*
  • Leukocytes / metabolism
  • Leukocytes / pathology
  • Mice
  • Myeloid Cells / immunology*
  • Myeloid Cells / metabolism
  • Myeloid Cells / pathology
  • Phenotype
  • Plaque, Atherosclerotic*
  • RNA-Seq*
  • Single-Cell Analysis*
  • Transcriptome*