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Effects of (–)-Loliolide against Fine Dust Preconditioned Keratinocyte Media-Induced Dermal Fibroblast Inflammation

At present air pollution in parts of East Asia is at an alarming level due to elevated levels of fine dust (FD). Other than pulmonary complications, FD was found to affect the pathogenesis of ROS-dependent inflammatory responses via penetrating barrier-disrupted skin, leading to degradation of extra...

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Autores principales: Fernando, Ilekuttige Priyan Shanura, Dias, Mawalle Kankanamge Hasitha Madhawa, Madusanka, Dissanayaka Mudiyanselage Dinesh, Kim, Hyun-Soo, Han, Eui-Jeong, Kim, Min-Ju, Seo, Min-Jeong, Ahn, Ginnae
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8144948/
https://www.ncbi.nlm.nih.gov/pubmed/33925954
http://dx.doi.org/10.3390/antiox10050675
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author Fernando, Ilekuttige Priyan Shanura
Dias, Mawalle Kankanamge Hasitha Madhawa
Madusanka, Dissanayaka Mudiyanselage Dinesh
Kim, Hyun-Soo
Han, Eui-Jeong
Kim, Min-Ju
Seo, Min-Jeong
Ahn, Ginnae
author_facet Fernando, Ilekuttige Priyan Shanura
Dias, Mawalle Kankanamge Hasitha Madhawa
Madusanka, Dissanayaka Mudiyanselage Dinesh
Kim, Hyun-Soo
Han, Eui-Jeong
Kim, Min-Ju
Seo, Min-Jeong
Ahn, Ginnae
author_sort Fernando, Ilekuttige Priyan Shanura
collection PubMed
description At present air pollution in parts of East Asia is at an alarming level due to elevated levels of fine dust (FD). Other than pulmonary complications, FD was found to affect the pathogenesis of ROS-dependent inflammatory responses via penetrating barrier-disrupted skin, leading to degradation of extracellular matrix components through the keratinocyte-fibroblast axis. The present study discloses the evaluation of human dermal fibroblast (HDF) responses to FD preconditioned human keratinocyte media (HPM) primed without and with (-)-loliolide (HTT). HPM-FD treatment increased the ROS level in HDFs and activated mitogen-activated protein kinase-derived nuclear factor (NF)-κB inflammatory signaling pathways with a minor reduction of viability. The above events led to cell differentiation and production of matrix metalloproteinases (MMP), increasing collagenase and elastase activity despite the increase of tissue inhibitors of metalloproteinases (TIMP). Media from HTT primed keratinocytes stimulated with FD indicated ameliorated levels of MMPs, inflammatory cytokines, and chemokines in HDFs with suppressed collagenase and elastase activity. Present observations help to understand the factors that affect HDFs in the microenvironment of FD exposed keratinocytes and the therapeutic role of HTT as a suppressor of skin aging. Further studies using organotypic skin culture models could broaden the understanding of the effects of FD and the therapeutic role of HTT.
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spelling pubmed-81449482021-05-26 Effects of (–)-Loliolide against Fine Dust Preconditioned Keratinocyte Media-Induced Dermal Fibroblast Inflammation Fernando, Ilekuttige Priyan Shanura Dias, Mawalle Kankanamge Hasitha Madhawa Madusanka, Dissanayaka Mudiyanselage Dinesh Kim, Hyun-Soo Han, Eui-Jeong Kim, Min-Ju Seo, Min-Jeong Ahn, Ginnae Antioxidants (Basel) Article At present air pollution in parts of East Asia is at an alarming level due to elevated levels of fine dust (FD). Other than pulmonary complications, FD was found to affect the pathogenesis of ROS-dependent inflammatory responses via penetrating barrier-disrupted skin, leading to degradation of extracellular matrix components through the keratinocyte-fibroblast axis. The present study discloses the evaluation of human dermal fibroblast (HDF) responses to FD preconditioned human keratinocyte media (HPM) primed without and with (-)-loliolide (HTT). HPM-FD treatment increased the ROS level in HDFs and activated mitogen-activated protein kinase-derived nuclear factor (NF)-κB inflammatory signaling pathways with a minor reduction of viability. The above events led to cell differentiation and production of matrix metalloproteinases (MMP), increasing collagenase and elastase activity despite the increase of tissue inhibitors of metalloproteinases (TIMP). Media from HTT primed keratinocytes stimulated with FD indicated ameliorated levels of MMPs, inflammatory cytokines, and chemokines in HDFs with suppressed collagenase and elastase activity. Present observations help to understand the factors that affect HDFs in the microenvironment of FD exposed keratinocytes and the therapeutic role of HTT as a suppressor of skin aging. Further studies using organotypic skin culture models could broaden the understanding of the effects of FD and the therapeutic role of HTT. MDPI 2021-04-26 /pmc/articles/PMC8144948/ /pubmed/33925954 http://dx.doi.org/10.3390/antiox10050675 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Fernando, Ilekuttige Priyan Shanura
Dias, Mawalle Kankanamge Hasitha Madhawa
Madusanka, Dissanayaka Mudiyanselage Dinesh
Kim, Hyun-Soo
Han, Eui-Jeong
Kim, Min-Ju
Seo, Min-Jeong
Ahn, Ginnae
Effects of (–)-Loliolide against Fine Dust Preconditioned Keratinocyte Media-Induced Dermal Fibroblast Inflammation
title Effects of (–)-Loliolide against Fine Dust Preconditioned Keratinocyte Media-Induced Dermal Fibroblast Inflammation
title_full Effects of (–)-Loliolide against Fine Dust Preconditioned Keratinocyte Media-Induced Dermal Fibroblast Inflammation
title_fullStr Effects of (–)-Loliolide against Fine Dust Preconditioned Keratinocyte Media-Induced Dermal Fibroblast Inflammation
title_full_unstemmed Effects of (–)-Loliolide against Fine Dust Preconditioned Keratinocyte Media-Induced Dermal Fibroblast Inflammation
title_short Effects of (–)-Loliolide against Fine Dust Preconditioned Keratinocyte Media-Induced Dermal Fibroblast Inflammation
title_sort effects of (–)-loliolide against fine dust preconditioned keratinocyte media-induced dermal fibroblast inflammation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8144948/
https://www.ncbi.nlm.nih.gov/pubmed/33925954
http://dx.doi.org/10.3390/antiox10050675
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