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 blockingDPPs using Val-boroPro triggers a lytic form of cell death in primary humanCD4 andCD8 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 theCARD8-caspase-1-GSDMDaxis. Moreover,DPP9 constitutes the relevantDPPrestrainingCARD8 activation. Interestingly, thisCARD8-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.
| Item Type: | Journal article |
|---|---|
| Faculties: | Chemistry and Pharmacy > Department of Biochemistry Medicine |
| Subjects: | 500 Science > 540 Chemistry 600 Technology > 610 Medicine and health |
| URN: | urn:nbn:de:bvb:19-epub-89711-2 |
| ISSN: | 0261-4189 |
| Language: | English |
| Item ID: | 89711 |
| Date Deposited: | 25. Jan 2022 09:32 |
| Last Modified: | 31. Aug 2023 12:51 |

