Cells of the adult human heart

Monika Litviňuková(Max Delbrück Center), Carlos Talavera‐López(European Bioinformatics Institute), Henrike Maatz(Max Delbrück Center), Daniel Reichart(Harvard University), Catherine L. Worth(Max Delbrück Center), Eric L. Lindberg(Max Delbrück Center), Masatoshi Kanda(Sapporo Medical University), Krzysztof Polański(Wellcome Sanger Institute), Matthias Heinig(Technical University of Munich), Michael Lee(Imperial College London), Emily R. Nadelmann(Harvard University), Kenny Roberts(Wellcome Sanger Institute), Elizabeth Tuck(Wellcome Sanger Institute), Eirini S. Fasouli(Wellcome Sanger Institute), Daniel M. DeLaughter(Harvard University), Barbara McDonough(Brigham and Women's Hospital), Hiroko Wakimoto(Harvard University), Joshua Gorham(Harvard University), Sara Samari(Imperial College London), Krishnaa T. Mahbubani(University of Cambridge), Kourosh Saeb‐Parsy(University of Cambridge), Giannino Patone(Max Delbrück Center), Joseph J. Boyle(Imperial College London), Hongbo Zhang(University of Alberta), Hao Zhang(University of Alberta), Anissa Viveiros(University of Alberta), Gavin Y. Oudit(University of Alberta), Omer Ali Bayraktar(Wellcome Sanger Institute), Jonathan G. Seidman(Harvard University), Christine E. Seidman(Brigham and Women's Hospital), Michela Noseda(British Heart Foundation), Norbert Hübner(Max Delbrück Center), Sarah A. Teichmann(University of Cambridge)
Nature
September 24, 2020
Cited by 1,748Open Access
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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.


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