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Cells of the adult human heart.
Litvinuková, Monika; Talavera-López, Carlos; Maatz, Henrike; Reichart, Daniel; Worth, Catherine L; Lindberg, Eric L; Kanda, Masatoshi; Polanski, Krzysztof; Heinig, Matthias; Lee, Michael; Nadelmann, Emily R; Roberts, Kenny; Tuck, Liz; Fasouli, Eirini S; DeLaughter, Daniel M; McDonough, Barbara; Wakimoto, Hiroko; Gorham, Joshua M; Samari, Sara; Mahbubani, Krishnaa T; Saeb-Parsy, Kourosh; Patone, Giannino; Boyle, Joseph J; Zhang, Hongbo; Zhang, Hao; Viveiros, Anissa; Oudit, Gavin Y; Bayraktar, Omer Ali; Seidman, J G; Seidman, Christine E; Noseda, Michela; Hubner, Norbert; Teichmann, Sarah A.
Afiliação
  • Litvinuková M; Cellular Genetics Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
  • Talavera-López C; Cardiovascular and Metabolic Sciences, Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin, Germany.
  • Maatz H; Cellular Genetics Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
  • Reichart D; EMBL - EBI, Wellcome Genome Campus, Hinxton, UK.
  • Worth CL; Cardiovascular and Metabolic Sciences, Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin, Germany.
  • Lindberg EL; Department of Genetics, Harvard Medical School, Boston, MA, USA.
  • Kanda M; Department of Cardiology, University Heart & Vascular Center, University of Hamburg, Hamburg, Germany.
  • Polanski K; Cardiovascular and Metabolic Sciences, Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin, Germany.
  • Heinig M; Cardiovascular and Metabolic Sciences, Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin, Germany.
  • Lee M; Cardiovascular and Metabolic Sciences, Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin, Germany.
  • Nadelmann ER; Department of Rheumatology and Clinical Immunology, Sapporo Medical University, Sapporo, Japan.
  • Roberts K; Cellular Genetics Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
  • Tuck L; Institute of Computational Biology (ICB), HMGU, Neuherberg, Germany.
  • Fasouli ES; Department of Informatics, Technische Universitaet Muenchen (TUM), Munich, Germany.
  • DeLaughter DM; National Heart and Lung Institute, Imperial College London, London, UK.
  • McDonough B; Department of Genetics, Harvard Medical School, Boston, MA, USA.
  • Wakimoto H; Cellular Genetics Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
  • Gorham JM; Cellular Genetics Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
  • Samari S; Cellular Genetics Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
  • Mahbubani KT; Department of Genetics, Harvard Medical School, Boston, MA, USA.
  • Saeb-Parsy K; Department of Genetics, Harvard Medical School, Boston, MA, USA.
  • Patone G; Cardiovascular Division, Brigham and Women's Hospital, Boston, MA, USA.
  • Boyle JJ; Howard Hughes Medical Institute, Chevy Chase, MD, USA.
  • Zhang H; Department of Genetics, Harvard Medical School, Boston, MA, USA.
  • Zhang H; Department of Genetics, Harvard Medical School, Boston, MA, USA.
  • Viveiros A; National Heart and Lung Institute, Imperial College London, London, UK.
  • Oudit GY; Department of Surgery, University of Cambridge, NIHR Cambridge Biomedical Centre, Cambridge Biorepository for Translational Medicine, Cambridge, UK.
  • Bayraktar OA; Department of Surgery, University of Cambridge, NIHR Cambridge Biomedical Centre, Cambridge Biorepository for Translational Medicine, Cambridge, UK.
  • Seidman JG; Cardiovascular and Metabolic Sciences, Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin, Germany.
  • Seidman CE; National Heart and Lung Institute, Imperial College London, London, UK.
  • Noseda M; Cellular Genetics Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
  • Hubner N; Department of Histology and Embryology of Zhongshan School of Medicine, Sun-Yat Sen University, Guangzhou, China.
  • Teichmann SA; Division of Cardiology, Department of Medicine, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Alberta, Canada.
Nature ; 588(7838): 466-472, 2020 12.
Article em En | MEDLINE | ID: mdl-32971526
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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Análise de Célula Única / Transcriptoma / Miocárdio Idioma: En Revista: Nature Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Análise de Célula Única / Transcriptoma / Miocárdio Idioma: En Revista: Nature Ano de publicação: 2020 Tipo de documento: Article