Author
Listed:
- Maximilian Strunz
(Helmholtz Zentrum Muenchen, Member of the German Center for Lung Research (DZL))
- Lukas M. Simon
(Helmholtz Zentrum München
University of Texas Health Science Center)
- Meshal Ansari
(Helmholtz Zentrum Muenchen, Member of the German Center for Lung Research (DZL)
Helmholtz Zentrum München)
- Jaymin J. Kathiriya
(University of California San Francisco)
- Ilias Angelidis
(Helmholtz Zentrum Muenchen, Member of the German Center for Lung Research (DZL))
- Christoph H. Mayr
(Helmholtz Zentrum Muenchen, Member of the German Center for Lung Research (DZL))
- George Tsidiridis
(Helmholtz Zentrum München)
- Marius Lange
(Helmholtz Zentrum München
Technische Universität München)
- Laura F. Mattner
(Helmholtz Zentrum Muenchen, Member of the German Center for Lung Research (DZL))
- Min Yee
(University of Rochester)
- Paulina Ogar
(Helmholtz Zentrum Muenchen, Member of the German Center for Lung Research (DZL))
- Arunima Sengupta
(Helmholtz Zentrum Muenchen, Member of the German Center for Lung Research (DZL))
- Igor Kukhtevich
(Institute of Functional Epigenetics, Helmholtz Zentrum München)
- Robert Schneider
(Institute of Functional Epigenetics, Helmholtz Zentrum München)
- Zhongming Zhao
(University of Texas Health Science Center)
- Carola Voss
(Helmholtz Zentrum Muenchen, Member of the German Center for Lung Research (DZL))
- Tobias Stoeger
(Helmholtz Zentrum Muenchen, Member of the German Center for Lung Research (DZL))
- Jens H. L. Neumann
(Institute of Pathology, Ludwig Maximilians University Hospital Munich)
- Anne Hilgendorff
(Helmholtz Zentrum Muenchen, Member of the German Center for Lung Research (DZL)
Hospital of the Ludwig-Maximilians University (LMU))
- Jürgen Behr
(Helmholtz Zentrum Muenchen, Member of the German Center for Lung Research (DZL)
Ludwig Maximilians University Hospital (LMU) Munich
Asklepios Fachkliniken in Munich-Gauting)
- Michael O’Reilly
(University of Rochester)
- Mareike Lehmann
(Helmholtz Zentrum München, Member of the German Center for Lung Research (DZL))
- Gerald Burgstaller
(Helmholtz Zentrum Muenchen, Member of the German Center for Lung Research (DZL))
- Melanie Königshoff
(Helmholtz Zentrum München, Member of the German Center for Lung Research (DZL)
University of Colorado, Department of Pulmonary Sciences and Critical Care Medicine)
- Harold A. Chapman
(University of California San Francisco)
- Fabian J. Theis
(Helmholtz Zentrum München
Technische Universität München)
- Herbert B. Schiller
(Helmholtz Zentrum Muenchen, Member of the German Center for Lung Research (DZL))
Abstract
The cell type specific sequences of transcriptional programs during lung regeneration have remained elusive. Using time-series single cell RNA-seq of the bleomycin lung injury model, we resolved transcriptional dynamics for 28 cell types. Trajectory modeling together with lineage tracing revealed that airway and alveolar stem cells converge on a unique Krt8 + transitional stem cell state during alveolar regeneration. These cells have squamous morphology, feature p53 and NFkB activation and display transcriptional features of cellular senescence. The Krt8+ state appears in several independent models of lung injury and persists in human lung fibrosis, creating a distinct cell–cell communication network with mesenchyme and macrophages during repair. We generated a model of gene regulatory programs leading to Krt8+ transitional cells and their terminal differentiation to alveolar type-1 cells. We propose that in lung fibrosis, perturbed molecular checkpoints on the way to terminal differentiation can cause aberrant persistence of regenerative intermediate stem cell states.
Suggested Citation
Maximilian Strunz & Lukas M. Simon & Meshal Ansari & Jaymin J. Kathiriya & Ilias Angelidis & Christoph H. Mayr & George Tsidiridis & Marius Lange & Laura F. Mattner & Min Yee & Paulina Ogar & Arunima , 2020.
"Alveolar regeneration through a Krt8+ transitional stem cell state that persists in human lung fibrosis,"
Nature Communications, Nature, vol. 11(1), pages 1-20, December.
Handle:
RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-17358-3
DOI: 10.1038/s41467-020-17358-3
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