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Regeneration of functional alveoli by adult human SOX9(+) airway basal cell transplantation
Irreversible destruction of bronchi and alveoli can lead to multiple incurable lung diseases. Identifying lung stem/progenitor cells with regenerative capacity and utilizing them to reconstruct functional tissue is one of the biggest hopes to reverse the damage and cure such diseases. Here we showed...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Higher Education Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5829276/ https://www.ncbi.nlm.nih.gov/pubmed/29344809 http://dx.doi.org/10.1007/s13238-018-0506-y |
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author | Ma, Qiwang Ma, Yu Dai, Xiaotian Ren, Tao Fu, Yingjie Liu, Wenbin Han, Yufei Wu, Yingchuan Cheng, Yu Zhang, Ting Zuo, Wei |
author_facet | Ma, Qiwang Ma, Yu Dai, Xiaotian Ren, Tao Fu, Yingjie Liu, Wenbin Han, Yufei Wu, Yingchuan Cheng, Yu Zhang, Ting Zuo, Wei |
author_sort | Ma, Qiwang |
collection | PubMed |
description | Irreversible destruction of bronchi and alveoli can lead to multiple incurable lung diseases. Identifying lung stem/progenitor cells with regenerative capacity and utilizing them to reconstruct functional tissue is one of the biggest hopes to reverse the damage and cure such diseases. Here we showed that a rare population of SOX9(+) basal cells (BCs) located at airway epithelium rugae can regenerate adult human lung. Human SOX9(+) BCs can be readily isolated by bronchoscopic brushing and indefinitely expanded in feeder-free condition. Expanded human SOX9(+) BCs can give rise to alveolar and bronchiolar epithelium after being transplanted into injured mouse lung, with air-blood exchange system reconstructed and recipient’s lung function improved. Manipulation of lung microenvironment with Pirfenidone to suppress TGF-β signaling could further boost the transplantation efficiency. Moreover, we conducted the first autologous SOX9(+) BCs transplantation clinical trial in two bronchiectasis patients. Lung tissue repair and pulmonary function enhancement was observed in patients 3–12 months after cell transplantation. Altogether our current work indicated that functional adult human lung structure can be reconstituted by orthotopic transplantation of tissue-specific stem/progenitor cells, which could be translated into a mature regenerative therapeutic strategy in near future. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s13238-018-0506-y) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5829276 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Higher Education Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-58292762018-02-28 Regeneration of functional alveoli by adult human SOX9(+) airway basal cell transplantation Ma, Qiwang Ma, Yu Dai, Xiaotian Ren, Tao Fu, Yingjie Liu, Wenbin Han, Yufei Wu, Yingchuan Cheng, Yu Zhang, Ting Zuo, Wei Protein Cell Research Article Irreversible destruction of bronchi and alveoli can lead to multiple incurable lung diseases. Identifying lung stem/progenitor cells with regenerative capacity and utilizing them to reconstruct functional tissue is one of the biggest hopes to reverse the damage and cure such diseases. Here we showed that a rare population of SOX9(+) basal cells (BCs) located at airway epithelium rugae can regenerate adult human lung. Human SOX9(+) BCs can be readily isolated by bronchoscopic brushing and indefinitely expanded in feeder-free condition. Expanded human SOX9(+) BCs can give rise to alveolar and bronchiolar epithelium after being transplanted into injured mouse lung, with air-blood exchange system reconstructed and recipient’s lung function improved. Manipulation of lung microenvironment with Pirfenidone to suppress TGF-β signaling could further boost the transplantation efficiency. Moreover, we conducted the first autologous SOX9(+) BCs transplantation clinical trial in two bronchiectasis patients. Lung tissue repair and pulmonary function enhancement was observed in patients 3–12 months after cell transplantation. Altogether our current work indicated that functional adult human lung structure can be reconstituted by orthotopic transplantation of tissue-specific stem/progenitor cells, which could be translated into a mature regenerative therapeutic strategy in near future. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s13238-018-0506-y) contains supplementary material, which is available to authorized users. Higher Education Press 2018-01-17 2018-03 /pmc/articles/PMC5829276/ /pubmed/29344809 http://dx.doi.org/10.1007/s13238-018-0506-y Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Research Article Ma, Qiwang Ma, Yu Dai, Xiaotian Ren, Tao Fu, Yingjie Liu, Wenbin Han, Yufei Wu, Yingchuan Cheng, Yu Zhang, Ting Zuo, Wei Regeneration of functional alveoli by adult human SOX9(+) airway basal cell transplantation |
title | Regeneration of functional alveoli by adult human SOX9(+) airway basal cell transplantation |
title_full | Regeneration of functional alveoli by adult human SOX9(+) airway basal cell transplantation |
title_fullStr | Regeneration of functional alveoli by adult human SOX9(+) airway basal cell transplantation |
title_full_unstemmed | Regeneration of functional alveoli by adult human SOX9(+) airway basal cell transplantation |
title_short | Regeneration of functional alveoli by adult human SOX9(+) airway basal cell transplantation |
title_sort | regeneration of functional alveoli by adult human sox9(+) airway basal cell transplantation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5829276/ https://www.ncbi.nlm.nih.gov/pubmed/29344809 http://dx.doi.org/10.1007/s13238-018-0506-y |
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