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Time-resolved role of P2X4 and P2X7 during CD8+ T cell activation.
Brock, Valerie J; Lory, Niels Christian; Möckl, Franziska; Birus, Melina; Stähler, Tobias; Woelk, Lena-Marie; Jaeckstein, Michelle; Heeren, Joerg; Koch-Nolte, Friedrich; Rissiek, Björn; Mittrücker, Hans-Willi; Guse, Andreas H; Werner, René; Diercks, Björn-Philipp.
Affiliation
  • Brock VJ; The Calcium Signalling Group, Department of Biochemistry and Molecular Cell Biology, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
  • Lory NC; Department of Immunology, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
  • Möckl F; The Calcium Signalling Group, Department of Biochemistry and Molecular Cell Biology, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
  • Birus M; Department of Immunology, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
  • Stähler T; Department of Immunology, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
  • Woelk LM; Department of Applied Medical Informatics, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
  • Jaeckstein M; Department of Computational Neuroscience, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
  • Heeren J; Department of Biochemistry and Molecular Cell Biology, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
  • Koch-Nolte F; Department of Biochemistry and Molecular Cell Biology, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
  • Rissiek B; Department of Immunology, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
  • Mittrücker HW; Department of Neurology, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
  • Guse AH; Department of Immunology, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
  • Werner R; The Calcium Signalling Group, Department of Biochemistry and Molecular Cell Biology, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
  • Diercks BP; Department of Applied Medical Informatics, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
Front Immunol ; 15: 1258119, 2024.
Article in En | MEDLINE | ID: mdl-38426095
ABSTRACT
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 Ca2+ microdomains. Recently, purinergic signaling was shown to be involved in the formation of the initial Ca2+ 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 Ca2+ microdomains, global Ca2+ responses, NFAT-1 translocation, cytokine expression, and proliferation. While Ca2+ microdomain formation was significantly reduced in the first milliseconds to seconds in CD8+ T cells lacking P2X4 and P2X7 channels, global Ca2+ 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 Ca2+ concentration ([Ca2+]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-γ, 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 Ca2+ 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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Signal Transduction / CD8-Positive T-Lymphocytes Language: En Journal: Front Immunol Year: 2024 Type: Article Affiliation country: Germany

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Signal Transduction / CD8-Positive T-Lymphocytes Language: En Journal: Front Immunol Year: 2024 Type: Article Affiliation country: Germany