Identification of a novel PPARβ/δ/miR-21-3p axis in UV-induced skin inflammation.

Fiche du document

Date

2016

Type de document
Périmètre
Langue
Identifiants
Relations

Ce document est lié à :
info:eu-repo/semantics/altIdentifier/doi/10.15252/emmm.201505384

Ce document est lié à :
info:eu-repo/semantics/altIdentifier/pmid/27250636

Ce document est lié à :
info:eu-repo/semantics/altIdentifier/eissn/1757-4684

Ce document est lié à :
info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_EC0CAB1654894

Licences

info:eu-repo/semantics/openAccess , Copying allowed only for non-profit organizations , https://serval.unil.ch/disclaimer



Sujets proches En

Integument (Skin) Cutis

Citer ce document

G. Degueurce et al., « Identification of a novel PPARβ/δ/miR-21-3p axis in UV-induced skin inflammation. », Serveur académique Lausannois, ID : 10.15252/emmm.201505384


Métriques


Partage / Export

Résumé 0

Although excessive exposure to UV is widely recognized as a major factor leading to skin perturbations and cancer, the complex mechanisms underlying inflammatory skin disorders resulting from UV exposure remain incompletely characterized. The nuclear hormone receptor PPARβ/δ is known to control mouse cutaneous repair and UV-induced skin cancer development. Here, we describe a novel PPARβ/δ-dependent molecular cascade involving TGFβ1 and miR-21-3p, which is activated in the epidermis in response to UV exposure. We establish that the passenger miRNA miR-21-3p, that we identify as a novel UV-induced miRNA in the epidermis, plays a pro-inflammatory function in keratinocytes and that its high level of expression in human skin is associated with psoriasis and squamous cell carcinomas. Finally, we provide evidence that inhibition of miR-21-3p reduces UV-induced cutaneous inflammation in ex vivo human skin biopsies, thereby underlining the clinical relevance of miRNA-based topical therapies for cutaneous disorders.

document thumbnail

Par les mêmes auteurs

Sur les mêmes sujets

Exporter en