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RATIONALE: It is assumed that atherosclerotic arteries contain several macrophage subsets endowed with specific functions. The precise identity of these subsets is poorly characterized as they have been defined by the expression of a restricted number of markers. OBJECTIVE: We have applied single-cell RNA sequencing as an unbiased profiling strategy to interrogate and classify aortic macrophage heterogeneity at the single-cell level in atherosclerosis. METHOD AND RESULTS: aortas, indicating relevance of our findings in different stages of atherosclerosis and mouse models. CONCLUSIONS: These data unprecedentedly uncovered the transcriptional landscape and phenotypic heterogeneity of aortic macrophages and monocyte-derived dendritic cells in atherosclerotic and identified previously unrecognized macrophage populations and their gene expression signature, suggesting specialized functions. Our findings will open up novel opportunities to explore distinct myeloid cell populations and their functions in atherosclerosis.
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Cochain et al. (Thu,) studied this question.
www.synapsesocial.com/papers/69ff5585ef8139f8ff7756e2 — DOI: https://doi.org/10.1161/circresaha.117.312509
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:
Clément Cochain
Ehsan Vafadarnejad
Panagiota Arampatzi
Circulation Research
Technical University of Munich
La Jolla Institute for Immunology
Klinikum rechts der Isar
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