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Genetically engineered distal airway stem cell transplantation protects mice from pulmonary infection

Severe pulmonary infection is a major threat to human health accompanied by substantial medical costs, prolonged inpatient requirements, and high mortality rates. New antimicrobial therapeutic strategies are urgently required to address the emergence of antibiotic resistance and persistent bacterial...

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Autores principales: Zhou, Yue‐qing, Shi, Yun, Yang, Ling, Sun, Yu‐fen, Han, Yu‐fei, Zhao, Zi‐xian, Wang, Yu‐jia, Liu, Ying, Ma, Yu, Zhang, Ting, Ren, Tao, Dale, Tina P, Forsyth, Nicholas R, Jin, Fa‐guang, Qu, Jie‐ming, Zuo, Wei, Xu, Jin‐fu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6949487/
https://www.ncbi.nlm.nih.gov/pubmed/31782624
http://dx.doi.org/10.15252/emmm.201810233
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author Zhou, Yue‐qing
Shi, Yun
Yang, Ling
Sun, Yu‐fen
Han, Yu‐fei
Zhao, Zi‐xian
Wang, Yu‐jia
Liu, Ying
Ma, Yu
Zhang, Ting
Ren, Tao
Dale, Tina P
Forsyth, Nicholas R
Jin, Fa‐guang
Qu, Jie‐ming
Zuo, Wei
Xu, Jin‐fu
author_facet Zhou, Yue‐qing
Shi, Yun
Yang, Ling
Sun, Yu‐fen
Han, Yu‐fei
Zhao, Zi‐xian
Wang, Yu‐jia
Liu, Ying
Ma, Yu
Zhang, Ting
Ren, Tao
Dale, Tina P
Forsyth, Nicholas R
Jin, Fa‐guang
Qu, Jie‐ming
Zuo, Wei
Xu, Jin‐fu
author_sort Zhou, Yue‐qing
collection PubMed
description Severe pulmonary infection is a major threat to human health accompanied by substantial medical costs, prolonged inpatient requirements, and high mortality rates. New antimicrobial therapeutic strategies are urgently required to address the emergence of antibiotic resistance and persistent bacterial infections. In this study, we show that the constitutive expression of a native antimicrobial peptide LL‐37 in transgenic mice aids in clearing Pseudomonas aeruginosa (PAO1), a major pathogen of clinical pulmonary infection. Orthotopic transplantation of adult mouse distal airway stem cells (DASCs), genetically engineered to express LL‐37, into injured mouse lung foci enabled large‐scale incorporation of cells and long‐term release of the host defense peptide, protecting the mice from bacterial pneumonia and hypoxemia. Further, correlates of DASCs in adult humans were isolated, expanded, and genetically engineered to demonstrate successful construction of an anti‐infective artificial lung. Together, our stem cell‐based gene delivery therapeutic platform proposes a new strategy for addressing recurrent pulmonary infections with future translational opportunities.
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spelling pubmed-69494872020-01-10 Genetically engineered distal airway stem cell transplantation protects mice from pulmonary infection Zhou, Yue‐qing Shi, Yun Yang, Ling Sun, Yu‐fen Han, Yu‐fei Zhao, Zi‐xian Wang, Yu‐jia Liu, Ying Ma, Yu Zhang, Ting Ren, Tao Dale, Tina P Forsyth, Nicholas R Jin, Fa‐guang Qu, Jie‐ming Zuo, Wei Xu, Jin‐fu EMBO Mol Med Articles Severe pulmonary infection is a major threat to human health accompanied by substantial medical costs, prolonged inpatient requirements, and high mortality rates. New antimicrobial therapeutic strategies are urgently required to address the emergence of antibiotic resistance and persistent bacterial infections. In this study, we show that the constitutive expression of a native antimicrobial peptide LL‐37 in transgenic mice aids in clearing Pseudomonas aeruginosa (PAO1), a major pathogen of clinical pulmonary infection. Orthotopic transplantation of adult mouse distal airway stem cells (DASCs), genetically engineered to express LL‐37, into injured mouse lung foci enabled large‐scale incorporation of cells and long‐term release of the host defense peptide, protecting the mice from bacterial pneumonia and hypoxemia. Further, correlates of DASCs in adult humans were isolated, expanded, and genetically engineered to demonstrate successful construction of an anti‐infective artificial lung. Together, our stem cell‐based gene delivery therapeutic platform proposes a new strategy for addressing recurrent pulmonary infections with future translational opportunities. John Wiley and Sons Inc. 2019-11-29 2020-01-09 /pmc/articles/PMC6949487/ /pubmed/31782624 http://dx.doi.org/10.15252/emmm.201810233 Text en © 2019 The Authors. Published under the terms of the CC BY 4.0 license This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Zhou, Yue‐qing
Shi, Yun
Yang, Ling
Sun, Yu‐fen
Han, Yu‐fei
Zhao, Zi‐xian
Wang, Yu‐jia
Liu, Ying
Ma, Yu
Zhang, Ting
Ren, Tao
Dale, Tina P
Forsyth, Nicholas R
Jin, Fa‐guang
Qu, Jie‐ming
Zuo, Wei
Xu, Jin‐fu
Genetically engineered distal airway stem cell transplantation protects mice from pulmonary infection
title Genetically engineered distal airway stem cell transplantation protects mice from pulmonary infection
title_full Genetically engineered distal airway stem cell transplantation protects mice from pulmonary infection
title_fullStr Genetically engineered distal airway stem cell transplantation protects mice from pulmonary infection
title_full_unstemmed Genetically engineered distal airway stem cell transplantation protects mice from pulmonary infection
title_short Genetically engineered distal airway stem cell transplantation protects mice from pulmonary infection
title_sort genetically engineered distal airway stem cell transplantation protects mice from pulmonary infection
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6949487/
https://www.ncbi.nlm.nih.gov/pubmed/31782624
http://dx.doi.org/10.15252/emmm.201810233
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