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Cells of the adult human heart

Author

Listed:
  • Monika Litviňuková

    (Wellcome Genome Campus
    Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC))

  • Carlos Talavera-López

    (Wellcome Genome Campus
    EMBL - EBI, Wellcome Genome Campus)

  • Henrike Maatz

    (Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC))

  • Daniel Reichart

    (Harvard Medical School
    University Heart & Vascular Center, University of Hamburg)

  • Catherine L. Worth

    (Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC))

  • Eric L. Lindberg

    (Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC))

  • Masatoshi Kanda

    (Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC)
    Sapporo Medical University)

  • Krzysztof Polanski

    (Wellcome Genome Campus)

  • Matthias Heinig

    (Institute of Computational Biology (ICB), HMGU
    Technische Universitaet Muenchen (TUM))

  • Michael Lee

    (Imperial College London)

  • Emily R. Nadelmann

    (Harvard Medical School)

  • Kenny Roberts

    (Wellcome Genome Campus)

  • Liz Tuck

    (Wellcome Genome Campus)

  • Eirini S. Fasouli

    (Wellcome Genome Campus)

  • Daniel M. DeLaughter

    (Harvard Medical School)

  • Barbara McDonough

    (Harvard Medical School
    Cardiovascular Division, Brigham and Women’s Hospital
    Howard Hughes Medical Institute)

  • Hiroko Wakimoto

    (Harvard Medical School)

  • Joshua M. Gorham

    (Harvard Medical School)

  • Sara Samari

    (Imperial College London)

  • Krishnaa T. Mahbubani

    (University of Cambridge, NIHR Cambridge Biomedical Centre, Cambridge Biorepository for Translational Medicine)

  • Kourosh Saeb-Parsy

    (University of Cambridge, NIHR Cambridge Biomedical Centre, Cambridge Biorepository for Translational Medicine)

  • Giannino Patone

    (Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC))

  • Joseph J. Boyle

    (Imperial College London)

  • Hongbo Zhang

    (Wellcome Genome Campus
    Sun-Yat Sen University)

  • Hao Zhang

    (University of Alberta
    University of Alberta)

  • Anissa Viveiros

    (University of Alberta
    University of Alberta)

  • Gavin Y. Oudit

    (University of Alberta
    University of Alberta)

  • Omer Ali Bayraktar

    (Wellcome Genome Campus)

  • J. G. Seidman

    (Harvard Medical School)

  • Christine E. Seidman

    (Harvard Medical School
    Cardiovascular Division, Brigham and Women’s Hospital
    Howard Hughes Medical Institute)

  • Michela Noseda

    (Imperial College London
    Imperial College London)

  • Norbert Hubner

    (Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC)
    DZHK (German Centre for Cardiovascular Research), Partner Site Berlin
    Charité-Universitätsmedizin
    Berlin Institute of Health (BIH))

  • Sarah A. Teichmann

    (Wellcome Genome Campus
    University of Cambridge)

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.

Suggested Citation

  • Monika Litviňuková & Carlos Talavera-López & Henrike Maatz & Daniel Reichart & Catherine L. Worth & Eric L. Lindberg & Masatoshi Kanda & Krzysztof Polanski & Matthias Heinig & Michael Lee & Emily R. N, 2020. "Cells of the adult human heart," Nature, Nature, vol. 588(7838), pages 466-472, December.
  • Handle: RePEc:nat:nature:v:588:y:2020:i:7838:d:10.1038_s41586-020-2797-4
    DOI: 10.1038/s41586-020-2797-4
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