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Fish Scale Collagen Peptides Protect against CoCl(2)/TNF-α-Induced Cytotoxicity and Inflammation via Inhibition of ROS, MAPK, and NF-κB Pathways in HaCaT Cells
Skin diseases associated with inflammation or oxidative stress represent the most common problem in dermatology. The present study demonstrates that fish scale collagen peptides (FSCP) protect against CoCl(2)-induced cytotoxicity and TNF-α-induced inflammatory responses in human HaCaT keratinocyte c...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5498912/ https://www.ncbi.nlm.nih.gov/pubmed/28717410 http://dx.doi.org/10.1155/2017/9703609 |
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author | Subhan, Fazli Kang, Hae Yeong Lim, Yeseon Ikram, Muhammad Baek, Sun-Yong Jin, Songwan Jeong, Young Hun Kwak, Jong Young Yoon, Sik |
author_facet | Subhan, Fazli Kang, Hae Yeong Lim, Yeseon Ikram, Muhammad Baek, Sun-Yong Jin, Songwan Jeong, Young Hun Kwak, Jong Young Yoon, Sik |
author_sort | Subhan, Fazli |
collection | PubMed |
description | Skin diseases associated with inflammation or oxidative stress represent the most common problem in dermatology. The present study demonstrates that fish scale collagen peptides (FSCP) protect against CoCl(2)-induced cytotoxicity and TNF-α-induced inflammatory responses in human HaCaT keratinocyte cells. Our study is the first to report that FSCP increase cell viability and ameliorate oxidative injury in HaCaT cells through mechanisms mediated by the downregulation of key proinflammatory cytokines, namely, TNF-α, IL-1β, IL-8, and iNOS. FSCP also prevent cell apoptosis by repressing Bax expression, caspase-3 activity, and cytochrome c release and by upregulating Bcl-2 protein levels in CoCl(2)- or TNF-α-stimulated HaCaT cells. In addition, the inhibitory effects of FSCP on cytotoxicity and the induction of proinflammatory cytokine expression were found to be associated with suppression of the ROS, MAPK (p38/MAPK, ERK, and JNK), and NF-κB signaling pathways. Taken together, our data suggest that FSCP are useful as immunomodulatory agents in inflammatory or immune-mediated skin diseases. Furthermore, our results provide new insights into the potential therapeutic use of FSCP in the prevention and treatment of various oxidative- or inflammatory stress-related inflammation and injuries. |
format | Online Article Text |
id | pubmed-5498912 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-54989122017-07-17 Fish Scale Collagen Peptides Protect against CoCl(2)/TNF-α-Induced Cytotoxicity and Inflammation via Inhibition of ROS, MAPK, and NF-κB Pathways in HaCaT Cells Subhan, Fazli Kang, Hae Yeong Lim, Yeseon Ikram, Muhammad Baek, Sun-Yong Jin, Songwan Jeong, Young Hun Kwak, Jong Young Yoon, Sik Oxid Med Cell Longev Research Article Skin diseases associated with inflammation or oxidative stress represent the most common problem in dermatology. The present study demonstrates that fish scale collagen peptides (FSCP) protect against CoCl(2)-induced cytotoxicity and TNF-α-induced inflammatory responses in human HaCaT keratinocyte cells. Our study is the first to report that FSCP increase cell viability and ameliorate oxidative injury in HaCaT cells through mechanisms mediated by the downregulation of key proinflammatory cytokines, namely, TNF-α, IL-1β, IL-8, and iNOS. FSCP also prevent cell apoptosis by repressing Bax expression, caspase-3 activity, and cytochrome c release and by upregulating Bcl-2 protein levels in CoCl(2)- or TNF-α-stimulated HaCaT cells. In addition, the inhibitory effects of FSCP on cytotoxicity and the induction of proinflammatory cytokine expression were found to be associated with suppression of the ROS, MAPK (p38/MAPK, ERK, and JNK), and NF-κB signaling pathways. Taken together, our data suggest that FSCP are useful as immunomodulatory agents in inflammatory or immune-mediated skin diseases. Furthermore, our results provide new insights into the potential therapeutic use of FSCP in the prevention and treatment of various oxidative- or inflammatory stress-related inflammation and injuries. Hindawi 2017 2017-06-22 /pmc/articles/PMC5498912/ /pubmed/28717410 http://dx.doi.org/10.1155/2017/9703609 Text en Copyright © 2017 Fazli Subhan et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Subhan, Fazli Kang, Hae Yeong Lim, Yeseon Ikram, Muhammad Baek, Sun-Yong Jin, Songwan Jeong, Young Hun Kwak, Jong Young Yoon, Sik Fish Scale Collagen Peptides Protect against CoCl(2)/TNF-α-Induced Cytotoxicity and Inflammation via Inhibition of ROS, MAPK, and NF-κB Pathways in HaCaT Cells |
title | Fish Scale Collagen Peptides Protect against CoCl(2)/TNF-α-Induced Cytotoxicity and Inflammation via Inhibition of ROS, MAPK, and NF-κB Pathways in HaCaT Cells |
title_full | Fish Scale Collagen Peptides Protect against CoCl(2)/TNF-α-Induced Cytotoxicity and Inflammation via Inhibition of ROS, MAPK, and NF-κB Pathways in HaCaT Cells |
title_fullStr | Fish Scale Collagen Peptides Protect against CoCl(2)/TNF-α-Induced Cytotoxicity and Inflammation via Inhibition of ROS, MAPK, and NF-κB Pathways in HaCaT Cells |
title_full_unstemmed | Fish Scale Collagen Peptides Protect against CoCl(2)/TNF-α-Induced Cytotoxicity and Inflammation via Inhibition of ROS, MAPK, and NF-κB Pathways in HaCaT Cells |
title_short | Fish Scale Collagen Peptides Protect against CoCl(2)/TNF-α-Induced Cytotoxicity and Inflammation via Inhibition of ROS, MAPK, and NF-κB Pathways in HaCaT Cells |
title_sort | fish scale collagen peptides protect against cocl(2)/tnf-α-induced cytotoxicity and inflammation via inhibition of ros, mapk, and nf-κb pathways in hacat cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5498912/ https://www.ncbi.nlm.nih.gov/pubmed/28717410 http://dx.doi.org/10.1155/2017/9703609 |
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