Cardiovascular disease is the leading cause of death worldwide. Advanced insights into disease mechanisms and therapeutic strategies require a deeper understanding of the molecular processes involved in the healthy heart. Knowledge of the full repertoire of cardiac cells and their gene expression profiles is a fundamental first step in this endeavour. Here, using state-of-the-art analyses of large-scale single-cell and single-nucleus transcriptomes, we characterize six anatomical adult heart regions. Our results highlight the cellular heterogeneity of cardiomyocytes, pericytes and fibroblasts, and reveal distinct atrial and ventricular subsets of cells with diverse developmental origins and specialized properties. We define the complexity of the cardiac vasculature and its changes along the arterio-venous axis. In the immune compartment, we identify cardiac-resident macrophages with inflammatory and protective transcriptional signatures. Furthermore, analyses of cell-to-cell interactions highlight different networks of macrophages, fibroblasts and cardiomyocytes between atria and ventricles that are distinct from those of skeletal muscle. Our human cardiac cell atlas improves our understanding of the human heart and provides a valuable reference for future studies.

Litvinukova, M., Talavera-Lopez, C., Maatz, H., Reichart, D., Worth, C., Lindberg, E., et al. (2020). Cells of the adult human heart. NATURE, 588(7838), 466-472 [10.1038/s41586-020-2797-4].

Cells of the adult human heart

Fasouli E. S.;
2020

Abstract

Cardiovascular disease is the leading cause of death worldwide. Advanced insights into disease mechanisms and therapeutic strategies require a deeper understanding of the molecular processes involved in the healthy heart. Knowledge of the full repertoire of cardiac cells and their gene expression profiles is a fundamental first step in this endeavour. Here, using state-of-the-art analyses of large-scale single-cell and single-nucleus transcriptomes, we characterize six anatomical adult heart regions. Our results highlight the cellular heterogeneity of cardiomyocytes, pericytes and fibroblasts, and reveal distinct atrial and ventricular subsets of cells with diverse developmental origins and specialized properties. We define the complexity of the cardiac vasculature and its changes along the arterio-venous axis. In the immune compartment, we identify cardiac-resident macrophages with inflammatory and protective transcriptional signatures. Furthermore, analyses of cell-to-cell interactions highlight different networks of macrophages, fibroblasts and cardiomyocytes between atria and ventricles that are distinct from those of skeletal muscle. Our human cardiac cell atlas improves our understanding of the human heart and provides a valuable reference for future studies.
Articolo in rivista - Articolo scientifico
Adipocytes; Adult; Angiotensin-Converting Enzyme 2; Epithelial Cells; Epithelium; Female; Fibroblasts; Gene Expression Profiling; Genome-Wide Association Study; Heart Atria; Heart Ventricles; Homeostasis; Humans; Macrophages; Male; Muscle, Skeletal; Myocardium; Myocytes, Cardiac; Neurons; Pericytes; Receptors, Coronavirus; SARS-CoV-2; Single-Cell Analysis; Stromal Cells; Transcriptome
English
2020
588
7838
466
472
none
Litvinukova, M., Talavera-Lopez, C., Maatz, H., Reichart, D., Worth, C., Lindberg, E., et al. (2020). Cells of the adult human heart. NATURE, 588(7838), 466-472 [10.1038/s41586-020-2797-4].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/527749
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