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Role of Caffeic Acid on Collagen Production in Nasal Polyp-Derived Fibroblasts

OBJECTIVES: Caffeic acids are known to have anti-oxidant, anti-inflammatory, immunomodulatory, and tissue reparative effects. The purposes of this study were to determine the effect of caffeic acid on transforming growth factor (TGF) β1-induced myofibroblast differentiation and collagen production,...

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Autores principales: Chung, Seung Won, Park, Il-Ho, Hong, Sung-Moon, Cho, Jung-Sun, Moon, Jun-Hyeok, Kim, Tae Hoon, Lee, Heung-Man
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Otorhinolaryngology-Head and Neck Surgery 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4240487/
https://www.ncbi.nlm.nih.gov/pubmed/25436049
http://dx.doi.org/10.3342/ceo.2014.7.4.295
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author Chung, Seung Won
Park, Il-Ho
Hong, Sung-Moon
Cho, Jung-Sun
Moon, Jun-Hyeok
Kim, Tae Hoon
Lee, Heung-Man
author_facet Chung, Seung Won
Park, Il-Ho
Hong, Sung-Moon
Cho, Jung-Sun
Moon, Jun-Hyeok
Kim, Tae Hoon
Lee, Heung-Man
author_sort Chung, Seung Won
collection PubMed
description OBJECTIVES: Caffeic acids are known to have anti-oxidant, anti-inflammatory, immunomodulatory, and tissue reparative effects. The purposes of this study were to determine the effect of caffeic acid on transforming growth factor (TGF) β1-induced myofibroblast differentiation and collagen production, and to determine whether caffeic acid is involved in the antioxidant effect in nasal polyp-derived fibroblasts (NPDFs). METHODS: NPDFs were pretreated with caffeic acid (1-10 µM) for 2 hours and stimulated with TGF-β1 (5 ng/mL) for 24 hours. The expression of α-smooth muscle actin (SMA), collagen types I and III, and Nox4 mRNA was determined by a reverse transcription-polymerase chain reaction, and the expression of α-SMA protein was determined by actin ned by immunofluorescence microscopy. The amount of total soluble collagen production was analyzed by the Sircol collagen dye-binding assay. The reactive oxygen species (ROS) generated by NPDFs were determined using 2',7'-dichlorfluorescein-diacetate. siNox4 was used to determine the effect of Nox4. RESULTS: The expression of α-SMA and production of collagen were significantly increased following TGF-β1 treatment. In contrast, the level of expression of α-SMA and the level of production of collagen were decreased by pretreatment with caffeic acid. The activation of Nox4 and the subsequent production of ROS were also reduced by pretreatment with caffeic acid. The expression of α-SMA was prevented by inhibition of ROS generation with siNox4. CONCLUSION: Caffeic acid may inhibit TGF-β1-induced differentiation of fibroblasts into myofibroblasts and collagen production by regulating ROS.
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spelling pubmed-42404872014-12-01 Role of Caffeic Acid on Collagen Production in Nasal Polyp-Derived Fibroblasts Chung, Seung Won Park, Il-Ho Hong, Sung-Moon Cho, Jung-Sun Moon, Jun-Hyeok Kim, Tae Hoon Lee, Heung-Man Clin Exp Otorhinolaryngol Original Article OBJECTIVES: Caffeic acids are known to have anti-oxidant, anti-inflammatory, immunomodulatory, and tissue reparative effects. The purposes of this study were to determine the effect of caffeic acid on transforming growth factor (TGF) β1-induced myofibroblast differentiation and collagen production, and to determine whether caffeic acid is involved in the antioxidant effect in nasal polyp-derived fibroblasts (NPDFs). METHODS: NPDFs were pretreated with caffeic acid (1-10 µM) for 2 hours and stimulated with TGF-β1 (5 ng/mL) for 24 hours. The expression of α-smooth muscle actin (SMA), collagen types I and III, and Nox4 mRNA was determined by a reverse transcription-polymerase chain reaction, and the expression of α-SMA protein was determined by actin ned by immunofluorescence microscopy. The amount of total soluble collagen production was analyzed by the Sircol collagen dye-binding assay. The reactive oxygen species (ROS) generated by NPDFs were determined using 2',7'-dichlorfluorescein-diacetate. siNox4 was used to determine the effect of Nox4. RESULTS: The expression of α-SMA and production of collagen were significantly increased following TGF-β1 treatment. In contrast, the level of expression of α-SMA and the level of production of collagen were decreased by pretreatment with caffeic acid. The activation of Nox4 and the subsequent production of ROS were also reduced by pretreatment with caffeic acid. The expression of α-SMA was prevented by inhibition of ROS generation with siNox4. CONCLUSION: Caffeic acid may inhibit TGF-β1-induced differentiation of fibroblasts into myofibroblasts and collagen production by regulating ROS. Korean Society of Otorhinolaryngology-Head and Neck Surgery 2014-12 2014-11-14 /pmc/articles/PMC4240487/ /pubmed/25436049 http://dx.doi.org/10.3342/ceo.2014.7.4.295 Text en Copyright © 2014 by Korean Society of Otorhinolaryngology-Head and Neck Surgery. http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Chung, Seung Won
Park, Il-Ho
Hong, Sung-Moon
Cho, Jung-Sun
Moon, Jun-Hyeok
Kim, Tae Hoon
Lee, Heung-Man
Role of Caffeic Acid on Collagen Production in Nasal Polyp-Derived Fibroblasts
title Role of Caffeic Acid on Collagen Production in Nasal Polyp-Derived Fibroblasts
title_full Role of Caffeic Acid on Collagen Production in Nasal Polyp-Derived Fibroblasts
title_fullStr Role of Caffeic Acid on Collagen Production in Nasal Polyp-Derived Fibroblasts
title_full_unstemmed Role of Caffeic Acid on Collagen Production in Nasal Polyp-Derived Fibroblasts
title_short Role of Caffeic Acid on Collagen Production in Nasal Polyp-Derived Fibroblasts
title_sort role of caffeic acid on collagen production in nasal polyp-derived fibroblasts
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4240487/
https://www.ncbi.nlm.nih.gov/pubmed/25436049
http://dx.doi.org/10.3342/ceo.2014.7.4.295
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