miR-21 is up-regulated in psoriasis and suppresses T cell apoptosis

F. Meisgen, Ning Xu, T. Wei, P.C. Janson, S. Obad, O. Broom, N. Nagy, Sakari Kauppinen, L. Kemény, M. Ståhle, A. Pivarcsi, E. Sonkoly

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139 Citations (Scopus)

Abstract

MicroRNAs are short non-coding RNAs that regulate gene expression. Previously, in a genome-wide screen, we found deregulation of microRNA expression in psoriasis skin. MicroRNA-21 (miR-21) is one of the microRNAs significantly up-regulated in psoriasis skin lesions. To identify the cell type responsible for the increased miR-21 level, we compared expression of miR-21 in epidermal cells and dermal T cells between psoriasis and healthy skin and found elevated levels of miR-21 in psoriasis in both cell types. In cultured T cells, expression of miR-21 increased markedly upon activation. To explore the function of miR-21 in primary human T helper cells, we inhibited miR-21 using a tiny seed-targeting LNA-anti-miR. Specific inhibition of miR-21 increased the apoptosis rate of activated T cells. Our results suggest that miR-21 suppresses apoptosis in activated T cells, and thus, overexpression of miR-21 may contribute to T cell-derived psoriatic skin inflammation.
Original languageEnglish
JournalExperimental Dermatology Online
Volume21
Issue number4
Pages (from-to)312-314
Number of pages3
ISSN1600-0625
DOIs
Publication statusPublished - 1 Apr 2012

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