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Categorization of lung mesenchymal cells in development and fibrosis
Pulmonary mesenchymal cells are critical players in both the mouse and human during lung development and disease states. They are increasingly recognized as highly heterogeneous, but there is no consensus on subpopulations or discriminative markers for each subtype. We completed scRNA-seq analysis o...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8188567/ https://www.ncbi.nlm.nih.gov/pubmed/34151224 http://dx.doi.org/10.1016/j.isci.2021.102551 |
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author | Liu, Xue Rowan, Simon C. Liang, Jiurong Yao, Changfu Huang, Guanling Deng, Nan Xie, Ting Wu, Di Wang, Yizhou Burman, Ankita Parimon, Tanyalak Borok, Zea Chen, Peter Parks, William C. Hogaboam, Cory M. Weigt, S. Samuel Belperio, John Stripp, Barry R. Noble, Paul W. Jiang, Dianhua |
author_facet | Liu, Xue Rowan, Simon C. Liang, Jiurong Yao, Changfu Huang, Guanling Deng, Nan Xie, Ting Wu, Di Wang, Yizhou Burman, Ankita Parimon, Tanyalak Borok, Zea Chen, Peter Parks, William C. Hogaboam, Cory M. Weigt, S. Samuel Belperio, John Stripp, Barry R. Noble, Paul W. Jiang, Dianhua |
author_sort | Liu, Xue |
collection | PubMed |
description | Pulmonary mesenchymal cells are critical players in both the mouse and human during lung development and disease states. They are increasingly recognized as highly heterogeneous, but there is no consensus on subpopulations or discriminative markers for each subtype. We completed scRNA-seq analysis of mesenchymal cells from the embryonic, postnatal, adult and aged fibrotic lungs of mice and humans. We consistently identified and delineated the transcriptome of lipofibroblasts, myofibroblasts, smooth muscle cells, pericytes, mesothelial cells, and a novel population characterized by Ebf1 expression. Subtype selective transcription factors and putative divergence of the clusters during development were described. Comparative analysis revealed orthologous subpopulations with conserved transcriptomic signatures in murine and human lung mesenchymal cells. All mesenchymal subpopulations contributed to matrix gene expression in fibrosis. This analysis would enhance our understanding of mesenchymal cell heterogeneity in lung development, homeostasis and fibrotic disease conditions. |
format | Online Article Text |
id | pubmed-8188567 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-81885672021-06-17 Categorization of lung mesenchymal cells in development and fibrosis Liu, Xue Rowan, Simon C. Liang, Jiurong Yao, Changfu Huang, Guanling Deng, Nan Xie, Ting Wu, Di Wang, Yizhou Burman, Ankita Parimon, Tanyalak Borok, Zea Chen, Peter Parks, William C. Hogaboam, Cory M. Weigt, S. Samuel Belperio, John Stripp, Barry R. Noble, Paul W. Jiang, Dianhua iScience Article Pulmonary mesenchymal cells are critical players in both the mouse and human during lung development and disease states. They are increasingly recognized as highly heterogeneous, but there is no consensus on subpopulations or discriminative markers for each subtype. We completed scRNA-seq analysis of mesenchymal cells from the embryonic, postnatal, adult and aged fibrotic lungs of mice and humans. We consistently identified and delineated the transcriptome of lipofibroblasts, myofibroblasts, smooth muscle cells, pericytes, mesothelial cells, and a novel population characterized by Ebf1 expression. Subtype selective transcription factors and putative divergence of the clusters during development were described. Comparative analysis revealed orthologous subpopulations with conserved transcriptomic signatures in murine and human lung mesenchymal cells. All mesenchymal subpopulations contributed to matrix gene expression in fibrosis. This analysis would enhance our understanding of mesenchymal cell heterogeneity in lung development, homeostasis and fibrotic disease conditions. Elsevier 2021-05-19 /pmc/articles/PMC8188567/ /pubmed/34151224 http://dx.doi.org/10.1016/j.isci.2021.102551 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Liu, Xue Rowan, Simon C. Liang, Jiurong Yao, Changfu Huang, Guanling Deng, Nan Xie, Ting Wu, Di Wang, Yizhou Burman, Ankita Parimon, Tanyalak Borok, Zea Chen, Peter Parks, William C. Hogaboam, Cory M. Weigt, S. Samuel Belperio, John Stripp, Barry R. Noble, Paul W. Jiang, Dianhua Categorization of lung mesenchymal cells in development and fibrosis |
title | Categorization of lung mesenchymal cells in development and fibrosis |
title_full | Categorization of lung mesenchymal cells in development and fibrosis |
title_fullStr | Categorization of lung mesenchymal cells in development and fibrosis |
title_full_unstemmed | Categorization of lung mesenchymal cells in development and fibrosis |
title_short | Categorization of lung mesenchymal cells in development and fibrosis |
title_sort | categorization of lung mesenchymal cells in development and fibrosis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8188567/ https://www.ncbi.nlm.nih.gov/pubmed/34151224 http://dx.doi.org/10.1016/j.isci.2021.102551 |
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