| First Author | Brock VJ | Year | 2024 |
| Journal | Front Immunol | Volume | 15 |
| Pages | 1258119 | PubMed ID | 38426095 |
| Mgi Jnum | J:345962 | Mgi Id | MGI:7608803 |
| Doi | 10.3389/fimmu.2024.1258119 | Citation | Brock VJ, et al. (2024) Time-resolved role of P2X4 and P2X7 during CD8(+) T cell activation. Front Immunol 15:1258119 |
| abstractText | CD8(+) T cells are a crucial part of the adaptive immune system, responsible for combating intracellular pathogens and tumor cells. The initial activation of T cells involves the formation of highly dynamic Ca(2+) microdomains. Recently, purinergic signaling was shown to be involved in the formation of the initial Ca(2+) microdomains in CD4(+) T cells. In this study, the role of purinergic cation channels, particularly P2X4 and P2X7, in CD8(+) T cell signaling from initial events to downstream responses was investigated, focusing on various aspects of T cell activation, including Ca(2+) microdomains, global Ca(2+) responses, NFAT-1 translocation, cytokine expression, and proliferation. While Ca(2+) microdomain formation was significantly reduced in the first milliseconds to seconds in CD8(+) T cells lacking P2X4 and P2X7 channels, global Ca(2+) responses over minutes were comparable between wild-type (WT) and knockout cells. However, the onset velocity was reduced in P2X4-deficient cells, and P2X4, as well as P2X7-deficient cells, exhibited a delayed response to reach a certain level of free cytosolic Ca(2+) concentration ([Ca(2+)](i)). NFAT-1 translocation, a crucial transcription factor in T cell activation, was also impaired in CD8(+) T cells lacking P2X4 and P2X7. In addition, the expression of IFN-gamma, a major pro-inflammatory cytokine produced by activated CD8(+) T cells, and Nur77, a negative regulator of T cell activation, was significantly reduced 18h post-stimulation in the knockout cells. In line, the proliferation of T cells after 3 days was also impaired in the absence of P2X4 and P2X7 channels. In summary, the study demonstrates that purinergic signaling through P2X4 and P2X7 enhances initial Ca(2+) events during CD8(+) T cell activation and plays a crucial role in regulating downstream responses, including NFAT-1 translocation, cytokine expression, and proliferation on multiple timescales. These findings suggest that targeting purinergic signaling pathways may offer potential therapeutic interventions. |
