Intrathymic programming of effector fates in three molecularly distinct γδ T cell subtypes (115.16)

التفاصيل البيبلوغرافية
العنوان: Intrathymic programming of effector fates in three molecularly distinct γδ T cell subtypes (115.16)
المؤلفون: Kavitha Narayan, Katelyn Sylvia, Nidhi Malhotra, Catherine Yin, Gregory Martens, Therese Vallerskog, Hardy Kornfeld, Na Xiong, Nadia Cohen, Michael Brenner, Leslie Berg, Joonsoo Kang, The Immunological Genome Project Consortium
المصدر: The Journal of Immunology. 188:115.16-115.16
بيانات النشر: The American Association of Immunologists, 2012.
سنة النشر: 2012
مصطلحات موضوعية: Immunology, Immunology and Allergy
الوصف: Two distinct lineages of T cells, distinguished by expression of either an αβ or γδ T cell receptor (TCR), arise from a common progenitor in the thymus. The type of pathogen and the cytokine milieu directs effector differentiation of αβ T cells in the periphery through the induction of specific transcriptional networks. γδ T cell development is distinct from that of αβ T cells in its ordered rearrangement of TCR genes and the pairing of Vγ and Vδ chains to generate γδ T cell subsets that home to specific tissues. While γδ T cells have primarily been studied as one homogenous population, they can be functionally classified into effector subsets based on the production of signature cytokines, analogous to αβ T helper subsets. Unlike αβ T cells, γδ T cell effector function correlates with genomically encoded TCR chains, but the mechanism of γδ effector specification is unclear. In conjunction with the Immunological Genome Project Consortium, we performed a high resolution transcriptome analysis of all emergent γδ thymocyte subsets segregated based on TCRγ/δ chain usage and maturation state in the thymus. Our data indicate the existence of three separate subtypes of γδ T cells in the thymus. The profiles of the emergent immature γδ T cell subsets are already embedded with unique gene programs directing subset-specific effector function, indicating that γδ T cell effector function is molecularly programmed in the thymus prior to, or concurrent with, TCR expression.
تدمد: 1550-6606
0022-1767
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::33f32a214ba15da624a1d67732649d54
https://doi.org/10.4049/jimmunol.188.supp.115.16
رقم الأكسشن: edsair.doi...........33f32a214ba15da624a1d67732649d54
قاعدة البيانات: OpenAIRE