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Abnormal respiratory progenitors in fibrotic lung injury
Recent advances in single-cell RNA sequencing (scRNA-seq) and epithelium lineage labeling have yielded identification of multiple abnormal epithelial progenitor populations during alveolar type 2 (ATII) cell differentiation into alveolar type 1 (ATI) cells during regenerative lung post-fibrotic inju...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8822870/ https://www.ncbi.nlm.nih.gov/pubmed/35130980 http://dx.doi.org/10.1186/s13287-022-02737-y |
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author | Xie, Ting Lynn, Heather Parks, William C. Stripp, Barry Chen, Peter Jiang, Dianhua Noble, Paul W. |
author_facet | Xie, Ting Lynn, Heather Parks, William C. Stripp, Barry Chen, Peter Jiang, Dianhua Noble, Paul W. |
author_sort | Xie, Ting |
collection | PubMed |
description | Recent advances in single-cell RNA sequencing (scRNA-seq) and epithelium lineage labeling have yielded identification of multiple abnormal epithelial progenitor populations during alveolar type 2 (ATII) cell differentiation into alveolar type 1 (ATI) cells during regenerative lung post-fibrotic injury. These abnormal cells include basaloid/basal-like cells, ATII transition cells, and persistent epithelial progenitors (PEPs). These cells occurred and accumulated during the regeneration of distal airway and alveoli in response to both chronic and acute pulmonary injury. Among the alveolar epithelial progenitors, PEPs express a distinct Krt8(+) phenotype that is rarely found in intact alveoli. However, post-injury, the Krt8(+) phenotype is seen in dysplastic epithelial cells. Fully understanding the characteristics and functions of these newly found, injury-induced abnormal behavioral epithelial progenitors and the signaling pathways regulating their phenotype could potentially point the way to unique therapeutic targets for fibrosing lung diseases. This review summarizes recent advances in understanding these epithelial progenitors as they relate to uncovering regenerative mechanisms. |
format | Online Article Text |
id | pubmed-8822870 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-88228702022-02-09 Abnormal respiratory progenitors in fibrotic lung injury Xie, Ting Lynn, Heather Parks, William C. Stripp, Barry Chen, Peter Jiang, Dianhua Noble, Paul W. Stem Cell Res Ther Review Recent advances in single-cell RNA sequencing (scRNA-seq) and epithelium lineage labeling have yielded identification of multiple abnormal epithelial progenitor populations during alveolar type 2 (ATII) cell differentiation into alveolar type 1 (ATI) cells during regenerative lung post-fibrotic injury. These abnormal cells include basaloid/basal-like cells, ATII transition cells, and persistent epithelial progenitors (PEPs). These cells occurred and accumulated during the regeneration of distal airway and alveoli in response to both chronic and acute pulmonary injury. Among the alveolar epithelial progenitors, PEPs express a distinct Krt8(+) phenotype that is rarely found in intact alveoli. However, post-injury, the Krt8(+) phenotype is seen in dysplastic epithelial cells. Fully understanding the characteristics and functions of these newly found, injury-induced abnormal behavioral epithelial progenitors and the signaling pathways regulating their phenotype could potentially point the way to unique therapeutic targets for fibrosing lung diseases. This review summarizes recent advances in understanding these epithelial progenitors as they relate to uncovering regenerative mechanisms. BioMed Central 2022-02-07 /pmc/articles/PMC8822870/ /pubmed/35130980 http://dx.doi.org/10.1186/s13287-022-02737-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Review Xie, Ting Lynn, Heather Parks, William C. Stripp, Barry Chen, Peter Jiang, Dianhua Noble, Paul W. Abnormal respiratory progenitors in fibrotic lung injury |
title | Abnormal respiratory progenitors in fibrotic lung injury |
title_full | Abnormal respiratory progenitors in fibrotic lung injury |
title_fullStr | Abnormal respiratory progenitors in fibrotic lung injury |
title_full_unstemmed | Abnormal respiratory progenitors in fibrotic lung injury |
title_short | Abnormal respiratory progenitors in fibrotic lung injury |
title_sort | abnormal respiratory progenitors in fibrotic lung injury |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8822870/ https://www.ncbi.nlm.nih.gov/pubmed/35130980 http://dx.doi.org/10.1186/s13287-022-02737-y |
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