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A Distinct Role for Interleukin‐6 as a Major Mediator of Cellular Adjustment to an Altered Culture Condition

Tissue microenvironment adjusts biological properties of different cells by modulating signaling pathways and cell to cell interactions. This study showed that epithelial–mesenchymal transition (EMT)/ mesenchymal–epithelial transition (MET) can be modulated by altering culture conditions. HPV E6/E7‐...

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Autores principales: Son, Hwa‐Kyung, Park, Iha, Kim, Jue Young, Kim, Do Kyeong, Illeperuma, Rasika P., Bae, Jung Yoon, Lee, Doo Young, Oh, Eun‐Sang, Jung, Da‐Woon, Williams, Darren R., Kim, Jin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4832257/
https://www.ncbi.nlm.nih.gov/pubmed/25939389
http://dx.doi.org/10.1002/jcb.25200
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author Son, Hwa‐Kyung
Park, Iha
Kim, Jue Young
Kim, Do Kyeong
Illeperuma, Rasika P.
Bae, Jung Yoon
Lee, Doo Young
Oh, Eun‐Sang
Jung, Da‐Woon
Williams, Darren R.
Kim, Jin
author_facet Son, Hwa‐Kyung
Park, Iha
Kim, Jue Young
Kim, Do Kyeong
Illeperuma, Rasika P.
Bae, Jung Yoon
Lee, Doo Young
Oh, Eun‐Sang
Jung, Da‐Woon
Williams, Darren R.
Kim, Jin
author_sort Son, Hwa‐Kyung
collection PubMed
description Tissue microenvironment adjusts biological properties of different cells by modulating signaling pathways and cell to cell interactions. This study showed that epithelial–mesenchymal transition (EMT)/ mesenchymal–epithelial transition (MET) can be modulated by altering culture conditions. HPV E6/E7‐transfected immortalized oral keratinocytes (IHOK) cultured in different media displayed reversible EMT/MET accompanied by changes in cell phenotype, proliferation, gene expression at transcriptional, and translational level, and migratory and invasive activities. Cholera toxin, a major supplement to culture medium, was responsible for inducing the morphological and biological changes of IHOK. Cholera toxin per se induced EMT by triggering the secretion of interleukin 6 (IL‐6) from IHOK. We found IL‐6 to be a central molecule that modulates the reversibility of EMT based not only on the mRNA level but also on the level of secretion. Taken together, our results demonstrate that IL‐6, a cytokine whose transcription is activated by alterations in culture conditions, is a key molecule for regulating reversible EMT/MET. This study will contribute to understand one way of cellular adjustment for surviving in unfamiliar conditions. J. Cell. Biochem. 116: 2552–2562, 2015. © 2015 The Authors. Journal of Cellular Biochemistry Published by Wiley Periodicals, Inc.
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spelling pubmed-48322572016-04-20 A Distinct Role for Interleukin‐6 as a Major Mediator of Cellular Adjustment to an Altered Culture Condition Son, Hwa‐Kyung Park, Iha Kim, Jue Young Kim, Do Kyeong Illeperuma, Rasika P. Bae, Jung Yoon Lee, Doo Young Oh, Eun‐Sang Jung, Da‐Woon Williams, Darren R. Kim, Jin J Cell Biochem Articles Tissue microenvironment adjusts biological properties of different cells by modulating signaling pathways and cell to cell interactions. This study showed that epithelial–mesenchymal transition (EMT)/ mesenchymal–epithelial transition (MET) can be modulated by altering culture conditions. HPV E6/E7‐transfected immortalized oral keratinocytes (IHOK) cultured in different media displayed reversible EMT/MET accompanied by changes in cell phenotype, proliferation, gene expression at transcriptional, and translational level, and migratory and invasive activities. Cholera toxin, a major supplement to culture medium, was responsible for inducing the morphological and biological changes of IHOK. Cholera toxin per se induced EMT by triggering the secretion of interleukin 6 (IL‐6) from IHOK. We found IL‐6 to be a central molecule that modulates the reversibility of EMT based not only on the mRNA level but also on the level of secretion. Taken together, our results demonstrate that IL‐6, a cytokine whose transcription is activated by alterations in culture conditions, is a key molecule for regulating reversible EMT/MET. This study will contribute to understand one way of cellular adjustment for surviving in unfamiliar conditions. J. Cell. Biochem. 116: 2552–2562, 2015. © 2015 The Authors. Journal of Cellular Biochemistry Published by Wiley Periodicals, Inc. John Wiley and Sons Inc. 2015-09-09 2015-11 /pmc/articles/PMC4832257/ /pubmed/25939389 http://dx.doi.org/10.1002/jcb.25200 Text en © 2015 The Authors. Journal of Cellular Biochemistry Published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Articles
Son, Hwa‐Kyung
Park, Iha
Kim, Jue Young
Kim, Do Kyeong
Illeperuma, Rasika P.
Bae, Jung Yoon
Lee, Doo Young
Oh, Eun‐Sang
Jung, Da‐Woon
Williams, Darren R.
Kim, Jin
A Distinct Role for Interleukin‐6 as a Major Mediator of Cellular Adjustment to an Altered Culture Condition
title A Distinct Role for Interleukin‐6 as a Major Mediator of Cellular Adjustment to an Altered Culture Condition
title_full A Distinct Role for Interleukin‐6 as a Major Mediator of Cellular Adjustment to an Altered Culture Condition
title_fullStr A Distinct Role for Interleukin‐6 as a Major Mediator of Cellular Adjustment to an Altered Culture Condition
title_full_unstemmed A Distinct Role for Interleukin‐6 as a Major Mediator of Cellular Adjustment to an Altered Culture Condition
title_short A Distinct Role for Interleukin‐6 as a Major Mediator of Cellular Adjustment to an Altered Culture Condition
title_sort distinct role for interleukin‐6 as a major mediator of cellular adjustment to an altered culture condition
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4832257/
https://www.ncbi.nlm.nih.gov/pubmed/25939389
http://dx.doi.org/10.1002/jcb.25200
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