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PM2.5 promotes human bronchial smooth muscle cell migration via the sonic hedgehog signaling pathway

BACKGROUND: The contribution of airway remodeling in chronic obstructive pulmonary disease (COPD) has been well documented, with airway smooth muscle cell proliferation and migration playing a role in the remodeling process. Here, we aimed to verify the effects of fine particulate matter (PM2.5) on...

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Autores principales: Ye, Xiuqin, Hong, Wei, Hao, Binwei, Peng, Gongyong, Huang, Lingmei, Zhao, Zhuxiang, Zhou, Yumin, Zheng, Mengning, Li, Chenglong, Liang, Chunxiao, Yi, Erkang, Pu, Jinding, Li, Bing, Ran, Pixin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5833105/
https://www.ncbi.nlm.nih.gov/pubmed/29499705
http://dx.doi.org/10.1186/s12931-017-0702-y
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author Ye, Xiuqin
Hong, Wei
Hao, Binwei
Peng, Gongyong
Huang, Lingmei
Zhao, Zhuxiang
Zhou, Yumin
Zheng, Mengning
Li, Chenglong
Liang, Chunxiao
Yi, Erkang
Pu, Jinding
Li, Bing
Ran, Pixin
author_facet Ye, Xiuqin
Hong, Wei
Hao, Binwei
Peng, Gongyong
Huang, Lingmei
Zhao, Zhuxiang
Zhou, Yumin
Zheng, Mengning
Li, Chenglong
Liang, Chunxiao
Yi, Erkang
Pu, Jinding
Li, Bing
Ran, Pixin
author_sort Ye, Xiuqin
collection PubMed
description BACKGROUND: The contribution of airway remodeling in chronic obstructive pulmonary disease (COPD) has been well documented, with airway smooth muscle cell proliferation and migration playing a role in the remodeling process. Here, we aimed to verify the effects of fine particulate matter (PM2.5) on human bronchial smooth muscle cell (HBSMC) migration and to explore the underlying signaling pathways. METHODS: HBSMC apoptosis, proliferation and migration were measured using flow cytometry, cell counting and transwell migration assays, respectively. The role of the hedgehog pathway in cell migration was assessed by western blotting to measure the expression of Sonic hedgehog (Shh), Gli1 and Snail. Furthermore, siRNA was used to knock down Gli1 or Snail expression. RESULTS: PM2.5 induced HBSMC apoptosis in a dose-dependent manner, although certain concentrations of PM2.5 did not induce HBSMC proliferation or apoptosis. Interestingly, cell migration was stimulated by PM2.5 doses far below those that induced apoptosis. Additional experiments revealed that these PM2.5 doses enhanced the expression of Shh, Gli1 and Snail in HBSMCs. Furthermore, PM2.5-induced cell migration and protein expression were enhanced by recombinant Shh and attenuated by cyclopamine. Similar results were obtained by knocking down Gli1 or Snail. CONCLUSIONS: These findings suggest that PM2.5, which may exert its effects through the Shh signaling pathway, is necessary for the migration of HBSMCs. These data define a novel role for PM2.5 in airway remodeling in COPD. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12931-017-0702-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-58331052018-03-05 PM2.5 promotes human bronchial smooth muscle cell migration via the sonic hedgehog signaling pathway Ye, Xiuqin Hong, Wei Hao, Binwei Peng, Gongyong Huang, Lingmei Zhao, Zhuxiang Zhou, Yumin Zheng, Mengning Li, Chenglong Liang, Chunxiao Yi, Erkang Pu, Jinding Li, Bing Ran, Pixin Respir Res Research BACKGROUND: The contribution of airway remodeling in chronic obstructive pulmonary disease (COPD) has been well documented, with airway smooth muscle cell proliferation and migration playing a role in the remodeling process. Here, we aimed to verify the effects of fine particulate matter (PM2.5) on human bronchial smooth muscle cell (HBSMC) migration and to explore the underlying signaling pathways. METHODS: HBSMC apoptosis, proliferation and migration were measured using flow cytometry, cell counting and transwell migration assays, respectively. The role of the hedgehog pathway in cell migration was assessed by western blotting to measure the expression of Sonic hedgehog (Shh), Gli1 and Snail. Furthermore, siRNA was used to knock down Gli1 or Snail expression. RESULTS: PM2.5 induced HBSMC apoptosis in a dose-dependent manner, although certain concentrations of PM2.5 did not induce HBSMC proliferation or apoptosis. Interestingly, cell migration was stimulated by PM2.5 doses far below those that induced apoptosis. Additional experiments revealed that these PM2.5 doses enhanced the expression of Shh, Gli1 and Snail in HBSMCs. Furthermore, PM2.5-induced cell migration and protein expression were enhanced by recombinant Shh and attenuated by cyclopamine. Similar results were obtained by knocking down Gli1 or Snail. CONCLUSIONS: These findings suggest that PM2.5, which may exert its effects through the Shh signaling pathway, is necessary for the migration of HBSMCs. These data define a novel role for PM2.5 in airway remodeling in COPD. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12931-017-0702-y) contains supplementary material, which is available to authorized users. BioMed Central 2018-03-02 2018 /pmc/articles/PMC5833105/ /pubmed/29499705 http://dx.doi.org/10.1186/s12931-017-0702-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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Ye, Xiuqin
Hong, Wei
Hao, Binwei
Peng, Gongyong
Huang, Lingmei
Zhao, Zhuxiang
Zhou, Yumin
Zheng, Mengning
Li, Chenglong
Liang, Chunxiao
Yi, Erkang
Pu, Jinding
Li, Bing
Ran, Pixin
PM2.5 promotes human bronchial smooth muscle cell migration via the sonic hedgehog signaling pathway
title PM2.5 promotes human bronchial smooth muscle cell migration via the sonic hedgehog signaling pathway
title_full PM2.5 promotes human bronchial smooth muscle cell migration via the sonic hedgehog signaling pathway
title_fullStr PM2.5 promotes human bronchial smooth muscle cell migration via the sonic hedgehog signaling pathway
title_full_unstemmed PM2.5 promotes human bronchial smooth muscle cell migration via the sonic hedgehog signaling pathway
title_short PM2.5 promotes human bronchial smooth muscle cell migration via the sonic hedgehog signaling pathway
title_sort pm2.5 promotes human bronchial smooth muscle cell migration via the sonic hedgehog signaling pathway
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5833105/
https://www.ncbi.nlm.nih.gov/pubmed/29499705
http://dx.doi.org/10.1186/s12931-017-0702-y
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