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Identification of chronological and photoageing-associated microRNAs in human skin

MicroRNAs are short non-coding RNAs that play key roles in regulating biological processes. In this study, we explored effects of chronological and photoageing on the miRNome of human skin. To this end, biopsies were collected from sun-exposed (outer arm, n = 45) and sun-protected (inner arm, n = 45...

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Autores principales: Srivastava, Ankit, Karlsson, Magnus, Marionnet, Claire, Bernerd, Françoise, Gueniche, Audrey, Rawadi, Charles E. l., Ståhle, Mona, Sonkoly, Enikö, Breton, Lionel, Pivarcsi, Andor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6113407/
https://www.ncbi.nlm.nih.gov/pubmed/30154427
http://dx.doi.org/10.1038/s41598-018-31217-8
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author Srivastava, Ankit
Karlsson, Magnus
Marionnet, Claire
Bernerd, Françoise
Gueniche, Audrey
Rawadi, Charles E. l.
Ståhle, Mona
Sonkoly, Enikö
Breton, Lionel
Pivarcsi, Andor
author_facet Srivastava, Ankit
Karlsson, Magnus
Marionnet, Claire
Bernerd, Françoise
Gueniche, Audrey
Rawadi, Charles E. l.
Ståhle, Mona
Sonkoly, Enikö
Breton, Lionel
Pivarcsi, Andor
author_sort Srivastava, Ankit
collection PubMed
description MicroRNAs are short non-coding RNAs that play key roles in regulating biological processes. In this study, we explored effects of chronological and photoageing on the miRNome of human skin. To this end, biopsies were collected from sun-exposed (outer arm, n = 45) and sun-protected (inner arm, n = 45) skin from fair-skinned (phototype II/III) healthy female volunteers of three age groups: young, 18–25 years, middle age, 40–50 years and aged, > 70 years. Strict inclusion criteria were used for photoageing scoring and for chronological ageing. Microarray analysis revealed that chronological ageing had minor effect on the human skin miRNome. In contrast, photoageing had a robust impact on miRNAs, and a set of miRNAs differentially expressed between sun-protected and sun-exposed skin of the young and aged groups was identified. Upregulation of miR-383, miR-145 and miR-34a and downregulation of miR-6879, miR-3648 and miR-663b were confirmed using qRT-PCR in sun-exposed skin compared with sun-protected skin. qRT-PCR analysis revealed that miR-383, miR-34a and miR-134 were differentially expressed in all three age groups both in chronological and photoageing, suggesting a synergetic effect of intrinsic and extrinsic ageing on their expression. In conclusion, our study identifies a unique miRNA signature which may contribute to skin ageing.
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spelling pubmed-61134072018-09-04 Identification of chronological and photoageing-associated microRNAs in human skin Srivastava, Ankit Karlsson, Magnus Marionnet, Claire Bernerd, Françoise Gueniche, Audrey Rawadi, Charles E. l. Ståhle, Mona Sonkoly, Enikö Breton, Lionel Pivarcsi, Andor Sci Rep Article MicroRNAs are short non-coding RNAs that play key roles in regulating biological processes. In this study, we explored effects of chronological and photoageing on the miRNome of human skin. To this end, biopsies were collected from sun-exposed (outer arm, n = 45) and sun-protected (inner arm, n = 45) skin from fair-skinned (phototype II/III) healthy female volunteers of three age groups: young, 18–25 years, middle age, 40–50 years and aged, > 70 years. Strict inclusion criteria were used for photoageing scoring and for chronological ageing. Microarray analysis revealed that chronological ageing had minor effect on the human skin miRNome. In contrast, photoageing had a robust impact on miRNAs, and a set of miRNAs differentially expressed between sun-protected and sun-exposed skin of the young and aged groups was identified. Upregulation of miR-383, miR-145 and miR-34a and downregulation of miR-6879, miR-3648 and miR-663b were confirmed using qRT-PCR in sun-exposed skin compared with sun-protected skin. qRT-PCR analysis revealed that miR-383, miR-34a and miR-134 were differentially expressed in all three age groups both in chronological and photoageing, suggesting a synergetic effect of intrinsic and extrinsic ageing on their expression. In conclusion, our study identifies a unique miRNA signature which may contribute to skin ageing. Nature Publishing Group UK 2018-08-28 /pmc/articles/PMC6113407/ /pubmed/30154427 http://dx.doi.org/10.1038/s41598-018-31217-8 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Srivastava, Ankit
Karlsson, Magnus
Marionnet, Claire
Bernerd, Françoise
Gueniche, Audrey
Rawadi, Charles E. l.
Ståhle, Mona
Sonkoly, Enikö
Breton, Lionel
Pivarcsi, Andor
Identification of chronological and photoageing-associated microRNAs in human skin
title Identification of chronological and photoageing-associated microRNAs in human skin
title_full Identification of chronological and photoageing-associated microRNAs in human skin
title_fullStr Identification of chronological and photoageing-associated microRNAs in human skin
title_full_unstemmed Identification of chronological and photoageing-associated microRNAs in human skin
title_short Identification of chronological and photoageing-associated microRNAs in human skin
title_sort identification of chronological and photoageing-associated micrornas in human skin
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6113407/
https://www.ncbi.nlm.nih.gov/pubmed/30154427
http://dx.doi.org/10.1038/s41598-018-31217-8
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