An integrated cell atlas of the human lung in health and disease

Lisa Sikkema(Helmholtz Zentrum München), Daniel Strobl(Helmholtz Zentrum München), Luke Zappia(Helmholtz Zentrum München), Elo Madissoon(Wellcome Sanger Institute), Nikolay S. Markov, Laure‐Emmanuelle Zaragosi(Centre National de la Recherche Scientifique), Meshal Ansari(Helmholtz Zentrum München), Marie‐Jeanne Arguel(Centre National de la Recherche Scientifique), Leonie Apperloo(University Medical Center Groningen), Christophe Bécavin(Centre National de la Recherche Scientifique), Marijn Berg(University Medical Center Groningen), Evgeny Chichelnitskiy(University of Bonn), Mei-I Chung(Translational Genomics Research Institute), Anne Collin(Centre National de la Recherche Scientifique), A.C.A. Gay(University Medical Center Groningen), Baharak Hooshiar Kashani(Helmholtz Zentrum München), Manu Jain, Theodoros Kapellos(Medizinische Hochschule Hannover), Tessa Kole(University Medical Center Groningen), Christoph H. Mayr(Helmholtz Zentrum München), Michael von Papen, L Peter(Translational Genomics Research Institute), Ciro Ramírez-Suástegui(Helmholtz Zentrum München), Janine Gote-Schniering(Helmholtz Zentrum München), Chase J. Taylor(Vanderbilt University Medical Center), Thomas Walzthoeni(Helmholtz Zentrum München), Chuan Xu(Wellcome Sanger Institute), LT Bui(Translational Genomics Research Institute), Carlo De Donno(Helmholtz Zentrum München), Leander Dony(Helmholtz Zentrum München), Minzhe Guo(Cincinnati Children's Hospital Medical Center), AJ Gutierrez(Translational Genomics Research Institute), Lukas Heumos(Helmholtz Zentrum München), Ni Huang(Wellcome Sanger Institute), Ignacio L. Ibarra(Helmholtz Zentrum München), Nathan D. Jackson(National Jewish Health), Preetish Kadur Lakshminarasimha Murthy(Duke University), Mohammad Lotfollahi(Helmholtz Zentrum München), Tracy Tabib(University of Pittsburgh Medical Center), Carlos Talavera‐López(Helmholtz Zentrum München), Kyle J. Travaglini(Stanford University), Anna Wilbrey-Clark(Wellcome Sanger Institute), KB Worlock(University College London), Masahiro Yoshida(Helmholtz Zentrum München), Tushar Desai(Stanford University), Oliver Eickelberg(University of Pittsburgh), Christine S. Falk(Medizinische Hochschule Hannover), Naftali Kaminski(Yale University), Mark A. Krasnow(Stanford University), Robert Lafyatis(University of Pittsburgh Medical Center), Marko Nikolić(University College London), J Powell(Garvan Institute of Medical Research), Jayaraj Rajagopal(Harvard University), Orit Rozenblatt–Rosen(Broad Institute), M.A. Seibold(National Jewish Health), Dean Sheppard(University of California, San Francisco), Douglas P. Shepherd(Arizona State University), SA Teichmann(Wellcome Sanger Institute), Alexander M. Tsankov(Icahn School of Medicine at Mount Sinai), J. A. Whitsett(Cincinnati Children's Hospital Medical Center), Yan Xu(Cincinnati Children's Hospital Medical Center), NE Banovich(Translational Genomics Research Institute), Pascal Barbry(Centre National de la Recherche Scientifique), TE Duong(University of California San Diego), KB Meyer(Wellcome Sanger Institute), JA Kropski(Vanderbilt University Medical Center), Dana Pe’er(Memorial Sloan Kettering Cancer Center), HB Schiller(Helmholtz Zentrum München), PR Tata(Duke University), Joachim L. Schultze(German Center for Neurodegenerative Diseases), AV Misharin, Martijn C. Nawijn(University Medical Center Groningen), Malte D. Luecken(Helmholtz Zentrum München), Fabian J. Theis(Helmholtz Zentrum München)
bioRxiv (Cold Spring Harbor Laboratory)
March 11, 2022
Cited by 97Open Access
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Abstract

ABSTRACT Organ- and body-scale cell atlases have the potential to transform our understanding of human biology. To capture the variability present in the population, these atlases must include diverse demographics such as age and ethnicity from both healthy and diseased individuals. The growth in both size and number of single-cell datasets, combined with recent advances in computational techniques, for the first time makes it possible to generate such comprehensive large-scale atlases through integration of multiple datasets. Here, we present the integrated Human Lung Cell Atlas (HLCA) combining 46 datasets of the human respiratory system into a single atlas spanning over 2.2 million cells from 444 individuals across health and disease. The HLCA contains a consensus re-annotation of published and newly generated datasets, resolving under- or misannotation of 59% of cells in the original datasets. The HLCA enables recovery of rare cell types, provides consensus marker genes for each cell type, and uncovers gene modules associated with demographic covariates and anatomical location within the respiratory system. To facilitate the use of the HLCA as a reference for single-cell lung research and allow rapid analysis of new data, we provide an interactive web portal to project datasets onto the HLCA. Finally, we demonstrate the value of the HLCA reference for interpreting disease-associated changes. Thus, the HLCA outlines a roadmap for the development and use of organ-scale cell atlases within the Human Cell Atlas.


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