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Protective influence of hyaluronic acid on focal adhesion kinase activity in human skin fibroblasts exposed to ethanol

AIM: The aim of this study was to evaluate the effect of ethanol and hyaluronic acid (HA) on cell survival and apoptosis in cultured human skin fibroblasts. Regarding the mechanism of ethanol action on human skin fibroblasts, we investigated cell viability and apoptosis, expression of focal adhesion...

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Autores principales: Donejko, Magdalena, Rysiak, Edyta, Galicka, Elżbieta, Terlikowski, Robert, Głażewska, Edyta Katarzyna, Przylipiak, Andrzej
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5345991/
https://www.ncbi.nlm.nih.gov/pubmed/28293103
http://dx.doi.org/10.2147/DDDT.S125843
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author Donejko, Magdalena
Rysiak, Edyta
Galicka, Elżbieta
Terlikowski, Robert
Głażewska, Edyta Katarzyna
Przylipiak, Andrzej
author_facet Donejko, Magdalena
Rysiak, Edyta
Galicka, Elżbieta
Terlikowski, Robert
Głażewska, Edyta Katarzyna
Przylipiak, Andrzej
author_sort Donejko, Magdalena
collection PubMed
description AIM: The aim of this study was to evaluate the effect of ethanol and hyaluronic acid (HA) on cell survival and apoptosis in cultured human skin fibroblasts. Regarding the mechanism of ethanol action on human skin fibroblasts, we investigated cell viability and apoptosis, expression of focal adhesion kinase (FAK), and the influence of HA on those processes. MATERIALS AND METHODS: Studies were conducted in confluent human skin fibroblast cultures that were treated with 25 mM, 50 mM, and 100 mM ethanol or with ethanol and 500 µg/mL HA. Cell viability was examined using methyl thiazolyl tetrazolium (MTT) assay and NC-300 Nucleo-Counter. Imaging of the cells using a fluorescence microscope Pathway 855 was performed to measure FAK expression. RESULTS: Depending on the dosage, ethanol decreased cell viability and activated the process of apoptosis in human skin fibroblasts. HA prevented the negative influence of ethanol on cell viability and prevented apoptosis. The analysis of fluorescence imaging using BD Pathway 855 High-Content Bioimager showed the inhibition of FAK migration to the cell nucleus, depending on the increasing concentration of ethanol. CONCLUSION: This study proves that downregulation of signaling pathway of FAK is involved in ethanol-induced apoptosis in human skin fibroblasts. The work also indicates a protective influence of HA on FAK activity in human skin fibroblasts exposed to ethanol.
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spelling pubmed-53459912017-03-14 Protective influence of hyaluronic acid on focal adhesion kinase activity in human skin fibroblasts exposed to ethanol Donejko, Magdalena Rysiak, Edyta Galicka, Elżbieta Terlikowski, Robert Głażewska, Edyta Katarzyna Przylipiak, Andrzej Drug Des Devel Ther Original Research AIM: The aim of this study was to evaluate the effect of ethanol and hyaluronic acid (HA) on cell survival and apoptosis in cultured human skin fibroblasts. Regarding the mechanism of ethanol action on human skin fibroblasts, we investigated cell viability and apoptosis, expression of focal adhesion kinase (FAK), and the influence of HA on those processes. MATERIALS AND METHODS: Studies were conducted in confluent human skin fibroblast cultures that were treated with 25 mM, 50 mM, and 100 mM ethanol or with ethanol and 500 µg/mL HA. Cell viability was examined using methyl thiazolyl tetrazolium (MTT) assay and NC-300 Nucleo-Counter. Imaging of the cells using a fluorescence microscope Pathway 855 was performed to measure FAK expression. RESULTS: Depending on the dosage, ethanol decreased cell viability and activated the process of apoptosis in human skin fibroblasts. HA prevented the negative influence of ethanol on cell viability and prevented apoptosis. The analysis of fluorescence imaging using BD Pathway 855 High-Content Bioimager showed the inhibition of FAK migration to the cell nucleus, depending on the increasing concentration of ethanol. CONCLUSION: This study proves that downregulation of signaling pathway of FAK is involved in ethanol-induced apoptosis in human skin fibroblasts. The work also indicates a protective influence of HA on FAK activity in human skin fibroblasts exposed to ethanol. Dove Medical Press 2017-03-06 /pmc/articles/PMC5345991/ /pubmed/28293103 http://dx.doi.org/10.2147/DDDT.S125843 Text en © 2017 Donejko et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Donejko, Magdalena
Rysiak, Edyta
Galicka, Elżbieta
Terlikowski, Robert
Głażewska, Edyta Katarzyna
Przylipiak, Andrzej
Protective influence of hyaluronic acid on focal adhesion kinase activity in human skin fibroblasts exposed to ethanol
title Protective influence of hyaluronic acid on focal adhesion kinase activity in human skin fibroblasts exposed to ethanol
title_full Protective influence of hyaluronic acid on focal adhesion kinase activity in human skin fibroblasts exposed to ethanol
title_fullStr Protective influence of hyaluronic acid on focal adhesion kinase activity in human skin fibroblasts exposed to ethanol
title_full_unstemmed Protective influence of hyaluronic acid on focal adhesion kinase activity in human skin fibroblasts exposed to ethanol
title_short Protective influence of hyaluronic acid on focal adhesion kinase activity in human skin fibroblasts exposed to ethanol
title_sort protective influence of hyaluronic acid on focal adhesion kinase activity in human skin fibroblasts exposed to ethanol
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5345991/
https://www.ncbi.nlm.nih.gov/pubmed/28293103
http://dx.doi.org/10.2147/DDDT.S125843
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