Key result
Single-cell and spatial transcriptomics reveal novel spatially resolved gene expression patterns in atherosclerosis and MI.
Why the study?
Single-cell and spatial transcriptomics have transformed cardiovascular research, warranting an overview of recent applications, emerging methods, and their impact on understanding cardiovascular disease.
Design
Review
May inform target discovery in atherosclerosis and MI; leaves open clinical adoption pending validation.
Single-cell and spatial transcriptomics technologies have transformed the landscape of cardiovascular research, leading to novel insights into cellular heterogeneity and tissue architecture in health and disease. These technologies enable researchers to deconvolute complex tissues and map gene expression patterns within their spatial contexts, providing critical information on the interplay between cell types and pathways affecting tissue regeneration or progression to fibrosis. This review presents an overview of the recently developed applications of single-cell and spatial transcriptomics methods and their impact on cardiovascular research. We discuss the principles underlying emerging solutions to process fixed and low-integrity RNA samples like formalin-fixed paraffin-embedded tissues. In addition, we highlight advances in high-resolution spatial transcriptomics assays, from imaging-based techniques like MERFISH (multiplexed error-robust fluorescence in situ hybridization) and Xenium to sequencing-based platforms like Visium HD, Stereo-seq, and Open-ST, each contributing unique strengths for tissue-level analysis. The integration of these technologies with machine learning and multiomics approaches further enhances the ability to uncover novel biology. These approaches have already led to the discovery of spatially resolved gene expression patterns in human atherosclerosis, hypertrophic cardiomyopathy, myocardial infarction, and myocarditis. These case studies showcase how these methods can be applied to decode the cellular and molecular dynamics of human disease processes, identify potential novel therapeutic targets, and enable predictive modeling of cellular perturbations and patient disease trajectories. We provide a comprehensive overview of the growing data repository landscape, the principles and applications of novel machine learning approaches, which are becoming more and more standard analytical tools. Integrating these areas underscores how recent advancements in single-cell and spatial transcriptomics are offering an increasingly detailed and comprehensive understanding of the cellular landscape of cardiovascular disease while also highlighting the challenges and future directions that will shape innovations in cardiovascular biology and medicine.
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Li et al. (2026) studied this question. Single-cell and spatial transcriptomics have unveiled novel spatially resolved gene expression patterns in human cardiovascular diseases like atherosclerosis and myocardial infarction.
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