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The negative costimulatory molecule PD-1 modulates the balance between immunity and tolerance via miR-21

✍ Scribed by Dimitrios Iliopoulos; Melina Kavousanaki; Marianna Ioannou; Dimitrios Boumpas; Panayotis Verginis


Book ID
102163607
Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
339 KB
Volume
41
Category
Article
ISSN
0014-2980

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✦ Synopsis


Abstract

Disruption of the programmed death‐1 (PD‐1) pathway leads to breakdown of peripheral tolerance and initiation of autoimmunity. The molecular pathways that mediate this effect remain largely unknown. We report here that PD‐1 knockout (PD‐1^−/−^) mice develop more severe and sustained Ag‐induced arthritis (AIA) than WT animals, which is associated with increased T‐cell proliferation and elevated levels of IFN‐γ and IL‐17 secretion. MicroRNA analysis of Ag‐specific CD4^+^ T cells revealed a significant upregulation of microRNA 21 (miR‐21) in PD‐1^−/−^ T cells compared with WT controls. In addition, PD‐1 inhibition, via siRNA, upregulated miR‐21 expression and enhanced STAT5 binding in the miR‐21 promoter area. Computational analysis confirmed that miR‐21 targets directly the expression of programmed cell death 4 (PDCD4) and overexpression of miR‐21 in cells harboring the 3′UTR of PDCD4 resulted in reduced transcription and PDCD4 protein expression. Importantly, in vitro delivery of antisense‐miR‐21 suppressed the Ag‐specific proliferation and cytokine secretion by PD‐1^−/−^ T cells, whereas adoptive transfer of Ag‐specific T cells, overexpressing miR‐21, induced severe AIA. Collectively, our data demonstrate that breakdown of tolerance in PD‐1^−/−^ mice activates a signaling cascade mediated by STAT5, miR‐21, and PDCD4 and establish their role in maintaining the balance between immune activation and tolerance.