1. Academic Validation
  2. CARD8 inflammasome activation triggers pyroptosis in human T cells

CARD8 inflammasome activation triggers pyroptosis in human T cells

  • EMBO J. 2020 Oct 1;39(19):e105071. doi: 10.15252/embj.2020105071.
Andreas Linder 1 2 Stefan Bauernfried 1 Yiming Cheng 1 Manuel Albanese 1 3 Christophe Jung 1 Oliver T Keppler 1 3 Veit Hornung 1
Affiliations

Affiliations

  • 1 Gene Center and Department of Biochemistry, Ludwig-Maximilians-Universität München, Munich, Germany.
  • 2 Department of Medicine II, University Hospital, Ludwig-Maximilians-Universität München, Munich, Germany.
  • 3 Max von Pettenkofer Institute, Virology, Ludwig-Maximilians-Universität München, Munich, Germany.
Abstract

Inflammasomes execute a unique type of cell death known as Pyroptosis. Mostly characterized in myeloid cells, Caspase-1 activation downstream of an inflammasome sensor results in the cleavage and activation of gasdermin D (GSDMD), which then forms a lytic pore in the plasma membrane. Recently, CARD8 was identified as a novel inflammasome sensor that triggers Pyroptosis in myeloid leukemia cells upon inhibition of dipeptidyl-peptidases (DPP). Here, we show that blocking DPPs using Val-boroPro triggers a lytic form of cell death in primary human CD4 and CD8 T cells, while other prototypical inflammasome stimuli were not active. This cell death displays morphological and biochemical hallmarks of Pyroptosis. By genetically dissecting candidate components in primary T cells, we identify this response to be dependent on the CARD8-caspase-1-GSDMD axis. Moreover, DPP9 constitutes the relevant DPP restraining CARD8 activation. Interestingly, this CARD8-induced Pyroptosis pathway can only be engaged in resting, but not in activated T cells. Altogether, these results broaden the relevance of inflammasome signaling and associated pyroptotic cell death to T cells, central players of the adaptive immune system.

Keywords

CARD8; T cell; Val-boroPro; inflammasome; pyroptosis.

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