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TWEAK enhances TGF-β-induced epithelial-mesenchymal transition in human bronchial epithelial cells

BACKGROUND: Chronic airway inflammatory disorders, such as asthma, are characterized by airway inflammation and remodeling. Chronic inflammation and damage to the airway epithelium cause airway remodeling, which is associated with improper epithelial repair, and is characterized by elevated expressi...

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Autores principales: Itoigawa, Yukinari, Harada, Norihiro, Harada, Sonoko, Katsura, Yoko, Makino, Fumihiko, Ito, Jun, Nurwidya, Fariz, Kato, Motoyasu, Takahashi, Fumiyuki, Atsuta, Ryo, Takahashi, Kazuhisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4397832/
https://www.ncbi.nlm.nih.gov/pubmed/25890309
http://dx.doi.org/10.1186/s12931-015-0207-5
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author Itoigawa, Yukinari
Harada, Norihiro
Harada, Sonoko
Katsura, Yoko
Makino, Fumihiko
Ito, Jun
Nurwidya, Fariz
Kato, Motoyasu
Takahashi, Fumiyuki
Atsuta, Ryo
Takahashi, Kazuhisa
author_facet Itoigawa, Yukinari
Harada, Norihiro
Harada, Sonoko
Katsura, Yoko
Makino, Fumihiko
Ito, Jun
Nurwidya, Fariz
Kato, Motoyasu
Takahashi, Fumiyuki
Atsuta, Ryo
Takahashi, Kazuhisa
author_sort Itoigawa, Yukinari
collection PubMed
description BACKGROUND: Chronic airway inflammatory disorders, such as asthma, are characterized by airway inflammation and remodeling. Chronic inflammation and damage to the airway epithelium cause airway remodeling, which is associated with improper epithelial repair, and is characterized by elevated expression of transforming growth factor-β (TGF-β). Epithelial-mesenchymal transition (EMT) is an important mechanism during embryonic development and tissue remodeling whereby epithelial cells gain the capacity to increase motility by down-regulation of epithelial markers and up-regulation of mesenchymal markers. TGF-β is a central inducer of EMT, and TGF-β-induced EMT is enhanced by pro-inflammatory cytokines, including tumor necrosis factor-α (TNF-α) and interleukin-1β. We investigated whether the pro-inflammatory cytokine TWEAK (TNF-like weak inducer of apoptosis) enhanced TGF-β1-induced EMT in the human bronchial epithelial cell line BEAS-2B. METHODS: Quantitative RT-PCR and western blotting were used to define alterations in epithelial and mesenchymal marker expression in BEAS-2B cells. The cells were assessed for 48 h after stimulation with TGF-β1 alone or in combination with TWEAK. RESULTS: TGF-β1 induced spindle-like morphology and loss of cell contact, and reduced the expression of epithelial marker E-cadherin and increased the expression of mesenchymal markers N-cadherin and vimentin. Our data, for the first time, show that TWEAK reduced the expression of E-cadherin, and that co-treatment with TGF-β1 and TWEAK enhanced the TGF-β1-induced features of EMT. Moreover, hyaluronan synthase 2 expression was up-regulated by a combination with TGF-β1 and TWEAK, but not TNF-α. We also demonstrated that the Smad, p38 MAPK, and NF-κB signaling pathways, and the transcriptional repressor ZEB2 might mediate N-cadherin up-regulation by TGF-β1 in combination with TWEAK. CONCLUSIONS: These findings suggest that the pro-inflammatory cytokine TWEAK and TGF-β1 have synergistic effects in EMT and may contribute to chronic airway changes and remodeling. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12931-015-0207-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-43978322015-04-16 TWEAK enhances TGF-β-induced epithelial-mesenchymal transition in human bronchial epithelial cells Itoigawa, Yukinari Harada, Norihiro Harada, Sonoko Katsura, Yoko Makino, Fumihiko Ito, Jun Nurwidya, Fariz Kato, Motoyasu Takahashi, Fumiyuki Atsuta, Ryo Takahashi, Kazuhisa Respir Res Research BACKGROUND: Chronic airway inflammatory disorders, such as asthma, are characterized by airway inflammation and remodeling. Chronic inflammation and damage to the airway epithelium cause airway remodeling, which is associated with improper epithelial repair, and is characterized by elevated expression of transforming growth factor-β (TGF-β). Epithelial-mesenchymal transition (EMT) is an important mechanism during embryonic development and tissue remodeling whereby epithelial cells gain the capacity to increase motility by down-regulation of epithelial markers and up-regulation of mesenchymal markers. TGF-β is a central inducer of EMT, and TGF-β-induced EMT is enhanced by pro-inflammatory cytokines, including tumor necrosis factor-α (TNF-α) and interleukin-1β. We investigated whether the pro-inflammatory cytokine TWEAK (TNF-like weak inducer of apoptosis) enhanced TGF-β1-induced EMT in the human bronchial epithelial cell line BEAS-2B. METHODS: Quantitative RT-PCR and western blotting were used to define alterations in epithelial and mesenchymal marker expression in BEAS-2B cells. The cells were assessed for 48 h after stimulation with TGF-β1 alone or in combination with TWEAK. RESULTS: TGF-β1 induced spindle-like morphology and loss of cell contact, and reduced the expression of epithelial marker E-cadherin and increased the expression of mesenchymal markers N-cadherin and vimentin. Our data, for the first time, show that TWEAK reduced the expression of E-cadherin, and that co-treatment with TGF-β1 and TWEAK enhanced the TGF-β1-induced features of EMT. Moreover, hyaluronan synthase 2 expression was up-regulated by a combination with TGF-β1 and TWEAK, but not TNF-α. We also demonstrated that the Smad, p38 MAPK, and NF-κB signaling pathways, and the transcriptional repressor ZEB2 might mediate N-cadherin up-regulation by TGF-β1 in combination with TWEAK. CONCLUSIONS: These findings suggest that the pro-inflammatory cytokine TWEAK and TGF-β1 have synergistic effects in EMT and may contribute to chronic airway changes and remodeling. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12931-015-0207-5) contains supplementary material, which is available to authorized users. BioMed Central 2015-04-08 2015 /pmc/articles/PMC4397832/ /pubmed/25890309 http://dx.doi.org/10.1186/s12931-015-0207-5 Text en © Itoigawa et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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
Itoigawa, Yukinari
Harada, Norihiro
Harada, Sonoko
Katsura, Yoko
Makino, Fumihiko
Ito, Jun
Nurwidya, Fariz
Kato, Motoyasu
Takahashi, Fumiyuki
Atsuta, Ryo
Takahashi, Kazuhisa
TWEAK enhances TGF-β-induced epithelial-mesenchymal transition in human bronchial epithelial cells
title TWEAK enhances TGF-β-induced epithelial-mesenchymal transition in human bronchial epithelial cells
title_full TWEAK enhances TGF-β-induced epithelial-mesenchymal transition in human bronchial epithelial cells
title_fullStr TWEAK enhances TGF-β-induced epithelial-mesenchymal transition in human bronchial epithelial cells
title_full_unstemmed TWEAK enhances TGF-β-induced epithelial-mesenchymal transition in human bronchial epithelial cells
title_short TWEAK enhances TGF-β-induced epithelial-mesenchymal transition in human bronchial epithelial cells
title_sort tweak enhances tgf-β-induced epithelial-mesenchymal transition in human bronchial epithelial cells
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4397832/
https://www.ncbi.nlm.nih.gov/pubmed/25890309
http://dx.doi.org/10.1186/s12931-015-0207-5
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