Abstract

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.

Highlights

  • Skin ageing is a complex process leading to decrement of cutaneous structures and functions with time

  • To investigate changes in the miRNome of the skin during photoageing and chronological ageing, RNA samples were obtained from the outer and the inner arm, representing sun-exposed and sun-protected skin, respectively, of healthy young, middle age and aged donors

  • The present study explored the impact of photoageing and chronological ageing on the miRNA signature of human skin

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Summary

Introduction

Skin ageing is a complex process leading to decrement of cutaneous structures and functions with time. Skin ageing involves two different processes: intrinsic (chronological) ageing, primarily determined by genetic factors, and extrinsic (photoageing) primarily due to solar UV exposure. The chronological ageing of human skin is characterized by increased laxity, fine wrinkling and dermal atrophy with reduced amounts of type I and III fibrillar collagens[1,2]. The extrinsic ageing of the skin is mainly caused by chronic solar exposure, which leads to alterations in biomolecules such as DNA, RNA and proteins. MiRNAs are involved in epidermal development, proliferation, differentiation[6,7,8,9,10,11], inflammatory responses, immune regulation[12], as well as in wound healing[13,14]. The aim of the present study was to explore the impact of chronological ageing and photoageing on the miRNome of human skin

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