| Literature DB >> 27306475 |
Laetitia Barbollat-Boutrand1,2,3, Nicolas Joly-Tonetti1,2,3, Morgan Dos Santos4, Elodie Metral4, Aurélie Boher5, Ingrid Masse1,2,3, Odile Berthier-Vergnes1,2,3, Philippe Bertolino6, Odile Damour4, Jérôme Lamartine1,2,3.
Abstract
MicroRNAs (miRNAs) are a class of short non-coding RNAs capable of repressing gene expression at the post-transcriptional level. miRNAs participate in the control of numerous cellular mechanisms, including skin homeostasis and epidermal differentiation. However, few miRNAs involved in these processes have been identified so far in human skin, and the gene networks they control remain largely unknown. Here, we focused on miR-23b-3p, a miRNA that is expressed during the late step of human keratinocyte differentiation. We report that miR-23b-3p silencing modulates epidermal differentiation in human skin reconstructs. The SMAD transcriptional corepressor TGIF1 was identified on bioinformatic analysis as a potential target of miR-23b-3p. Expression analysis and reporter gene assays confirmed direct regulation of TGIF1 expression by miR-23b-3p. Finally, we showed that miR-23-3p was able to activate TGF-ß signalling in human keratinocytes by increasing SMAD2 phosphorylation through TGIF1 repression. Taken together, these data identify miR-23b-3p as a new regulator of human epidermal differentiation in line with TGF-ß signalling.Entities:
Keywords: TGF-beta; differentiation; keratinocytes; microRNA
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Year: 2017 PMID: 27306475 DOI: 10.1111/exd.13119
Source DB: PubMed Journal: Exp Dermatol ISSN: 0906-6705 Impact factor: 3.960