Decoding Vascular Cell Diversity: Single-Cell Approaches to Mechanisms of Vascular Disease

Almost 200 years of histological and molecular analysis has established that functional shifts in vascular cell populations are associated with healthy vascular function and the progression of vascular disease. Now, new methods in single-cell analysis are serving to dramatically accelerate the study of vascular cell heterogeneity. Here, we will outline the experimental and computational technologies that have made high-throughput analysis of single cells possible, and review recent studies applying these approaches to vascular cells and tissues. In particular, the application of single-cell or single-nucleus RNA sequencing has identified rare and disease-specific cell populations, drivers of cellular heterogeneity, and specific vascular disease-relevant cell populations. High-throughput approaches linking CRISPR (clustered regularly interspaced short palindromic repeats) perturbations to single-cell RNA sequencing data are providing new insights into cell type-specific mechanisms of disease, and connecting human genetic data to these mechanisms. Other single-cell approaches are providing insights into regulatory mechanisms by linking chromatin accessibility to transcription in single cells and revealing the spatial positioning of rare cell types in vascular tissues. With a variety of well-established methods and the continued development of new technologies, single-cell approaches are becoming indispensable and powerful avenues for discovering and detailing new mechanisms of vascular disease.

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Publication Details

Journal
Circulation Research
Published
2026-01-02
DOI
https://doi.org/10.1161/circresaha.125.326001
Citations
1
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
22.24
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article

Decoding Vascular Cell Diversity: Single-Cell Approaches to Mechanisms of Vascular Disease

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1 citations
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Single-cell and spatial transcriptomics
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article

Decoding Vascular Cell Diversity: Single-Cell Approaches to Mechanisms of Vascular Disease

Helen Kang, Gavin R. Schnitzler, Jyoti Rao, Mark E. Pepin, William Schwartzman, Cindy X. Zheng, Mohita Maurya, Lily Widdup, Jiahao Jiang, Rajat M. Gupta
article en
1 citations

Abstract

Almost 200 years of histological and molecular analysis has established that functional shifts in vascular cell populations are associated with healthy vascular function and the progression of vascular disease. Now, new methods in single-cell analysis are serving to dramatically accelerate the study of vascular cell heterogeneity. Here, we will outline the experimental and computational technologies that have made high-throughput analysis of single cells possible, and review recent studies applying these approaches to vascular cells and tissues. In particular, the application of single-cell or single-nucleus RNA sequencing has identified rare and disease-specific cell populations, drivers of cellular heterogeneity, and specific vascular disease-relevant cell populations. High-throughput approaches linking CRISPR (clustered regularly interspaced short palindromic repeats) perturbations to single-cell RNA sequencing data are providing new insights into cell type-specific mechanisms of disease, and connecting human genetic data to these mechanisms. Other single-cell approaches are providing insights into regulatory mechanisms by linking chromatin accessibility to transcription in single cells and revealing the spatial positioning of rare cell types in vascular tissues. With a variety of well-established methods and the continued development of new technologies, single-cell approaches are becoming indispensable and powerful avenues for discovering and detailing new mechanisms of vascular disease.

Circulation ResearchVol. 138(1)
Broad Institute (US), Brigham and Women's Hospital (US)
Openalex Percentile: Top 4%
Single-cell and spatial transcriptomics
22.24
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