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Table 1 Single-cell studies of different atherosclerosis samples in human and mice

From: Emerging applications of single-cell profiling in precision medicine of atherosclerosis

Sample type

Species

Source

Methods

Major findings

References

Plaque

Human

Immune cells VSMCs

Endothelial cells

scRNA-seq,

scATAC-seq

The cellular landscape of human atherosclerotic plaques; cellular plasticity and intercellular communication at the site of disease

[26]

Human

Macrophages

CD4+ T cell

CD8+ T cell

CyTOF

CITE-seq

scRNA-seq

Novel immune dysregulation in plaques associated with the clinically symptomatic disease

T cell subsets present markers of T cell exhaustion

macrophages contain alternatively activated phenotypes

[43]

Human/Mice

Immune cells, VSMCs

CITE-seq

scRNA-seq

The transcriptome phenotype of SMCs in mouse and human atherosclerosis lesions is comprehensively characterized

TCF21 expression is closely associated with the regulation of SMC phenotype in diseased human coronary arteries

[89]

Mice

Macrophages

scRNA-seq

Prophagocyte single-walled carbon nanotubes reduce inflammatory gene expression in diseased macrophages

[117]

Mice

CD4+ T cells

scRNA-seq

Identification of CD4+ T cells that recognize apolipoprotein (apo) B in mice

[118]

Mice

Immune cells

CyTOF

scRNA-seq

The white blood cells from the aorta of healthy and atherosclerotic mice were deeply characterized; to determine the map of the immune cell landscape in atherosclerosis

[35]

Mice

Macrophages

scRNA-seq

Heterogeneity of macrophages during the progression and regression of atherosclerosis; stem cell-like characteristics of monocytes

[119]

Blood

Mice

VSMCs

scRNA-seq

Heterogeneity of VSMCs in blood vessels of healthy mice; characteristics of disease-related transcription in VSMCs lineage cells

[120]

Human

Monocyte

scRNA-seq

Humans have significant monocyte heterogeneity

[42]

Human

Red blood cells

scRNA-seq

RBC RNA-Seq capture; transcriptional heterogeneity of red blood cells

[41]

Human

Exosome Macrophage

scRNA-seq

Revealed the unique relationship between the transcription characteristics of macrophages and phenotypic heterogeneity in the microenvironment of atherosclerosis

[44]

Human

PBMCs

CITE-seq

The practicality of scRNA seq in evaluating cell surface phenotype in the same cell

[36]

Human

CD4+ T cells

scRNA-Seq, CITE-Seq

Gender differences in gene expression of CD4+ cells

[46]

Mice

Adipocytes

scRNA-seq

Changes in adipocyte function are the basis for observed changes in plasma lipids

[45]

Liver

Human

Liver cells

scRNA-seq

Map of the human liver immune microenvironment

[62, 63]

Mice

Adipocytes

scRNA-seq

Changes in adipocyte function are the basis for observed changes in plasma lipids

[45]

Mice

Myeloid cells

scRNA-seq

Heterogeneity of bone marrow cells in the liver and bone marrow during NAFLD; NAFLD has driven in vitro macrophage functional adaptation and its functional correlation during in vivo steatohepatitis

[64]

Intestine

Mice

Intestinal flora

16S ribosomal RNA gene sequencing

Bile acid has been identified as an important metabolic factor related to the gut microbiota

[68]

Mice

Fecal microorganisms

16S ribosomal RNA gene sequencing

PSRC1 participates in regulating the gut microbiome

[69]

  1. scRNA-seq single-cell RNA sequencing, scATAC-seq single-cell Assay for Transposase-Accessible Chromatin using sequencing, CyTOF Cytometry by Time-of-Flight; CITE-seq, Cellular indexing of transcriptomes and epitopes by sequencing, TCF21 transcription factor 21, CX3CR1 fractalkine receptor, VSMCs Vascular smooth muscle cells, PBMCs Peripheral Blood Mononuclear Cells, CAD Coronary Artery Disease, CVAV Cardiovascular Assessment Virginia, Trib1 tribbles homolog 1, NAFLD Non-alcoholic fatty liver disease, PSRC1 Proline/serine-rich coiled-coil protein