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Identification of ultraviolet B radiation-induced microRNAs in normal human dermal papilla cells

Ultraviolet (UV) radiation impairs intracellular functions by directly damaging DNA and by indirectly generating reactive oxygen species (ROS), which induce cell cycle arrest and apoptosis. UV radiation can also alter gene expression profiles, including those of mRNA and microRNA (miRNA). The effect...

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Autores principales: CHA, HWA JUN, KIM, OK-YEON, LEE, GANG TAI, LEE, KWANG SIK, LEE, JAE HO, PARK, IN-CHUL, LEE, SU-JAE, KIM, YU RI, AHN, KYU JOONG, AN, IN-SOOK, AN, SUNGKWAN, BAE, SEUNGHEE
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4148374/
https://www.ncbi.nlm.nih.gov/pubmed/25069581
http://dx.doi.org/10.3892/mmr.2014.2418
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author CHA, HWA JUN
KIM, OK-YEON
LEE, GANG TAI
LEE, KWANG SIK
LEE, JAE HO
PARK, IN-CHUL
LEE, SU-JAE
KIM, YU RI
AHN, KYU JOONG
AN, IN-SOOK
AN, SUNGKWAN
BAE, SEUNGHEE
author_facet CHA, HWA JUN
KIM, OK-YEON
LEE, GANG TAI
LEE, KWANG SIK
LEE, JAE HO
PARK, IN-CHUL
LEE, SU-JAE
KIM, YU RI
AHN, KYU JOONG
AN, IN-SOOK
AN, SUNGKWAN
BAE, SEUNGHEE
author_sort CHA, HWA JUN
collection PubMed
description Ultraviolet (UV) radiation impairs intracellular functions by directly damaging DNA and by indirectly generating reactive oxygen species (ROS), which induce cell cycle arrest and apoptosis. UV radiation can also alter gene expression profiles, including those of mRNA and microRNA (miRNA). The effects of UV radiation on cellular functions and gene expression have been widely documented in human skin cells such as keratinocytes, melanocytes and dermal fibroblasts, but the effect it has on other types of skin cell such as dermal papilla cells, which are crucial in the induction of hair follicle growth, remains unknown. In the current study, the effect of UV radiation on physiological changes and miRNA-based expression profiles in normal human dermal papilla cells (nHDPs) was investigated. UVB radiation of ≥50 mJ/cm(2) displayed high cytotoxicity and apoptosis in a dose-dependent manner. In addition, ROS generation was exhibited in UVB-irradiated nHDPs. Furthermore, using miRNA microarray analysis, it was demonstrated that the expression profiles of 42 miRNAs in UVB-irradiated nHDPs were significantly altered compared with those in the controls (35 upregulated and 7 downregulated). The biological functions of the differentially expressed miRNAs were studied with gene ontology analysis to identify their putative target mRNAs, and were demonstrated to be involved in cell survival- and death-related functions. Overall, the results of the present study provide evidence that miRNA-based cellular mechanisms may be involved in the UVB-induced cellular response in nHDPs.
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spelling pubmed-41483742014-08-29 Identification of ultraviolet B radiation-induced microRNAs in normal human dermal papilla cells CHA, HWA JUN KIM, OK-YEON LEE, GANG TAI LEE, KWANG SIK LEE, JAE HO PARK, IN-CHUL LEE, SU-JAE KIM, YU RI AHN, KYU JOONG AN, IN-SOOK AN, SUNGKWAN BAE, SEUNGHEE Mol Med Rep Articles Ultraviolet (UV) radiation impairs intracellular functions by directly damaging DNA and by indirectly generating reactive oxygen species (ROS), which induce cell cycle arrest and apoptosis. UV radiation can also alter gene expression profiles, including those of mRNA and microRNA (miRNA). The effects of UV radiation on cellular functions and gene expression have been widely documented in human skin cells such as keratinocytes, melanocytes and dermal fibroblasts, but the effect it has on other types of skin cell such as dermal papilla cells, which are crucial in the induction of hair follicle growth, remains unknown. In the current study, the effect of UV radiation on physiological changes and miRNA-based expression profiles in normal human dermal papilla cells (nHDPs) was investigated. UVB radiation of ≥50 mJ/cm(2) displayed high cytotoxicity and apoptosis in a dose-dependent manner. In addition, ROS generation was exhibited in UVB-irradiated nHDPs. Furthermore, using miRNA microarray analysis, it was demonstrated that the expression profiles of 42 miRNAs in UVB-irradiated nHDPs were significantly altered compared with those in the controls (35 upregulated and 7 downregulated). The biological functions of the differentially expressed miRNAs were studied with gene ontology analysis to identify their putative target mRNAs, and were demonstrated to be involved in cell survival- and death-related functions. Overall, the results of the present study provide evidence that miRNA-based cellular mechanisms may be involved in the UVB-induced cellular response in nHDPs. D.A. Spandidos 2014-10 2014-07-24 /pmc/articles/PMC4148374/ /pubmed/25069581 http://dx.doi.org/10.3892/mmr.2014.2418 Text en Copyright © 2014, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Articles
CHA, HWA JUN
KIM, OK-YEON
LEE, GANG TAI
LEE, KWANG SIK
LEE, JAE HO
PARK, IN-CHUL
LEE, SU-JAE
KIM, YU RI
AHN, KYU JOONG
AN, IN-SOOK
AN, SUNGKWAN
BAE, SEUNGHEE
Identification of ultraviolet B radiation-induced microRNAs in normal human dermal papilla cells
title Identification of ultraviolet B radiation-induced microRNAs in normal human dermal papilla cells
title_full Identification of ultraviolet B radiation-induced microRNAs in normal human dermal papilla cells
title_fullStr Identification of ultraviolet B radiation-induced microRNAs in normal human dermal papilla cells
title_full_unstemmed Identification of ultraviolet B radiation-induced microRNAs in normal human dermal papilla cells
title_short Identification of ultraviolet B radiation-induced microRNAs in normal human dermal papilla cells
title_sort identification of ultraviolet b radiation-induced micrornas in normal human dermal papilla cells
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4148374/
https://www.ncbi.nlm.nih.gov/pubmed/25069581
http://dx.doi.org/10.3892/mmr.2014.2418
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