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Intrapulmonary distal airway stem cell transplantation repairs lung injury in chronic obstructive pulmonary disease
OBJECTIVES: Chronic obstructive pulmonary disease (COPD) is characterized by irreversible lung tissue damage including chronic bronchitis and emphysema, which could further develop into respiratory failure. Many studies have revealed a potential regenerative function of the distal airway stem/progen...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8168420/ https://www.ncbi.nlm.nih.gov/pubmed/33960563 http://dx.doi.org/10.1111/cpr.13046 |
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author | Wang, Xiaofan Zhao, Yu Li, Dandan Feng, Yun Xie, Yusang Zhou, Yueqing Zhou, Min Wang, Yujia Qu, Jieming Zuo, Wei |
author_facet | Wang, Xiaofan Zhao, Yu Li, Dandan Feng, Yun Xie, Yusang Zhou, Yueqing Zhou, Min Wang, Yujia Qu, Jieming Zuo, Wei |
author_sort | Wang, Xiaofan |
collection | PubMed |
description | OBJECTIVES: Chronic obstructive pulmonary disease (COPD) is characterized by irreversible lung tissue damage including chronic bronchitis and emphysema, which could further develop into respiratory failure. Many studies have revealed a potential regenerative function of the distal airway stem/progenitor cells (DASCs) after lung injury. MATERIALS AND METHODS: Mouse and human DASCs were expanded, analysed, and engrafted into injured mouse lungs. Single‐cell analyses were performed to reveal the differentiation path of the engrafted cells. Finally, human DASCs were transplanted into COPD mice induced by porcine pancreatic elastase (PPE) and lipopolysaccharide (LPS) administration. RESULTS: We showed that isolated mouse and human DASCs could be indefinitely expanded and were able to further differentiate into mature alveolar structures in vitro. Single‐cell analysis indicated that the engrafted cells expressed typical cellular markers of type I alveolar cells as well as the specific secreted proteins. Interestingly, transplantation of human DASCs derived from COPD patients into the lungs of NOD‐SCID mice with COPD injury repaired the tissue damage and improved the pulmonary function. CONCLUSIONS: The findings demonstrated that functional lung structure could be reconstituted by intrapulmonary transplantation of DASCs, suggesting a potential therapeutic role of DASCs transplantation in treatment for chronic obstructive pulmonary disease. |
format | Online Article Text |
id | pubmed-8168420 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-81684202021-06-05 Intrapulmonary distal airway stem cell transplantation repairs lung injury in chronic obstructive pulmonary disease Wang, Xiaofan Zhao, Yu Li, Dandan Feng, Yun Xie, Yusang Zhou, Yueqing Zhou, Min Wang, Yujia Qu, Jieming Zuo, Wei Cell Prolif Original Articles OBJECTIVES: Chronic obstructive pulmonary disease (COPD) is characterized by irreversible lung tissue damage including chronic bronchitis and emphysema, which could further develop into respiratory failure. Many studies have revealed a potential regenerative function of the distal airway stem/progenitor cells (DASCs) after lung injury. MATERIALS AND METHODS: Mouse and human DASCs were expanded, analysed, and engrafted into injured mouse lungs. Single‐cell analyses were performed to reveal the differentiation path of the engrafted cells. Finally, human DASCs were transplanted into COPD mice induced by porcine pancreatic elastase (PPE) and lipopolysaccharide (LPS) administration. RESULTS: We showed that isolated mouse and human DASCs could be indefinitely expanded and were able to further differentiate into mature alveolar structures in vitro. Single‐cell analysis indicated that the engrafted cells expressed typical cellular markers of type I alveolar cells as well as the specific secreted proteins. Interestingly, transplantation of human DASCs derived from COPD patients into the lungs of NOD‐SCID mice with COPD injury repaired the tissue damage and improved the pulmonary function. CONCLUSIONS: The findings demonstrated that functional lung structure could be reconstituted by intrapulmonary transplantation of DASCs, suggesting a potential therapeutic role of DASCs transplantation in treatment for chronic obstructive pulmonary disease. John Wiley and Sons Inc. 2021-05-07 /pmc/articles/PMC8168420/ /pubmed/33960563 http://dx.doi.org/10.1111/cpr.13046 Text en © 2021 The Authors. Cell Proliferation Published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Wang, Xiaofan Zhao, Yu Li, Dandan Feng, Yun Xie, Yusang Zhou, Yueqing Zhou, Min Wang, Yujia Qu, Jieming Zuo, Wei Intrapulmonary distal airway stem cell transplantation repairs lung injury in chronic obstructive pulmonary disease |
title | Intrapulmonary distal airway stem cell transplantation repairs lung injury in chronic obstructive pulmonary disease |
title_full | Intrapulmonary distal airway stem cell transplantation repairs lung injury in chronic obstructive pulmonary disease |
title_fullStr | Intrapulmonary distal airway stem cell transplantation repairs lung injury in chronic obstructive pulmonary disease |
title_full_unstemmed | Intrapulmonary distal airway stem cell transplantation repairs lung injury in chronic obstructive pulmonary disease |
title_short | Intrapulmonary distal airway stem cell transplantation repairs lung injury in chronic obstructive pulmonary disease |
title_sort | intrapulmonary distal airway stem cell transplantation repairs lung injury in chronic obstructive pulmonary disease |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8168420/ https://www.ncbi.nlm.nih.gov/pubmed/33960563 http://dx.doi.org/10.1111/cpr.13046 |
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