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Advisor(s)
Abstract(s)
γδ T cells producing either interleukin-17A (γδ17 cells) or interferon-γ (γδIFN cells) are generated in the mouse thymus, but the molecular regulators of their peripheral functions are not fully characterized. Here we established an Il17a-GFP:Ifng-YFP double-reporter mouse strain to analyze at unprecedented depth the transcriptomes of pure γδ17 cell versus γδIFN cell populations from peripheral lymph nodes. Within a very high fraction of differentially expressed genes, we identify a panel of 20 new signature genes in steady-state γδ17 cells versus γδIFN cells, which we further validate in models of experimental autoimmune encephalomyelitis and cerebral malaria, respectively. Among the signature genes, we show that the co-receptor CD6 and the signaling protein Themis promote the activation and proliferation of peripheral γδIFN cells in response to T cell antigen receptor stimulation in vitro and to Plasmodium infection in vivo. This resource can help to understand the distinct activities of effector γδ T cell subsets in pathophysiology.
Description
Keywords
γδ T cells interleukin-17A (γδ17 cells) interferon-γ (γδIFN cells)
Pedagogical Context
Citation
Inácio, D., Amado, T., Pamplona, A., Sobral, D., Cunha, C., Santos, R. F., Oliveira, L., Rouquié, N., Carmo, A. M., Lesourne, R., Gomes, A. Q., & Silva-Santos, B. (2025). Signature cytokine-associated transcriptome analysis of effector γδ T cells identifies subset-specific regulators of peripheral activation. Nature Immunology, 26(3), 497–510. https://doi.org/10.1038/s41590-024-02073-8
Publisher
Springer Nature
