%0 Journal Article %9 ACL : Articles dans des revues avec comité de lecture répertoriées par l'AERES %A Abdallah, F. %A Henriet, E. %A Suet, A. %A Arar, A. %A Clemencon, R. %A Malinge, J. M. %A Lecellier, Gael %A Baril, P. %A Pichon, C. %T miR-21-3p/IL-22 axes are major drivers of psoriasis pathogenesis by modulating keratinocytes proliferation-survival balance and inflammatory response %D 2021 %L fdi:010083303 %G ENG %J Cells %K IL-22 ; miR-21-5p ; miR-21-3p ; keratinocytes ; psoriasis ; proliferation %M ISI:000713178400001 %N 10 %P 2547 [22 ] %R 10.3390/cells10102547 %U https://www.documentation.ird.fr/hor/fdi:010083303 %> https://horizon.documentation.ird.fr/exl-doc/pleins_textes/2021-12/010083303.pdf %V 10 %W Horizon (IRD) %X Psoriasis is a chronic inflammatory skin disease that is mediated by complex crosstalk between immune cells and keratinocytes (KCs). Emerging studies have showed a specific psoriatic microRNAs signature, in which miR-21 is one of the most upregulated and dynamic miRNAs. In this study, we focused our investigations on the passenger miR-21-3p strand, which is poorly studied in skin and in psoriasis pathogenesis. Here, we showed the upregulation of miR-21-3p in an IMQ-induced psoriasiform mouse model. This upregulation was correlated with IL-22 expression and functionality, both in vitro and in vivo, and it occurred via STAT3 and NF-kappa B signaling. We identified a network of differentially expressed genes involved in abnormal proliferation control and immune regulatory genes implicated in the molecular pathogenesis of psoriasis in response to miR-21-3p overexpression in KCs. These results were confirmed by functional assays that validated the proliferative potential of miR-21-3p. All these findings highlight the importance of miR-21-3p, an underestimated miRNA, in psoriasis and provide novel molecular targets for therapeutic purposes.

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