| Literature DB >> 25770130 |
Takeshi Nitta1, Ryunosuke Muro1, Yukiko Shimizu2, Sachiko Nitta1, Hiroyo Oda1, Yuki Ohte3, Motohito Goto2, Rieko Yanobu-Takanashi2, Tomoya Narita4, Hiroshi Takayanagi4, Hisataka Yasuda5, Tadashi Okamura6, Shigeo Murata3, Harumi Suzuki7.
Abstract
The thymus provides a specialized microenvironment in which distinct subsets of thymic epithelial cells (TECs) support T-cell development. Here, we describe the significance of cortical TECs (cTECs) in T-cell development, using a newly established mouse model of cTEC deficiency. The deficiency of mature cTECs caused a massive loss of thymic cellularity and impaired the development of αβT cells and invariant natural killer T cells. Unexpectedly, the differentiation of certain γδT-cell subpopulations-interleukin-17-producing Vγ4 and Vγ6 cells-was strongly dysregulated, resulting in the perturbation of γδT-mediated inflammatory responses in peripheral tissues. These findings show that cTECs contribute to the shaping of the TCR repertoire, not only of "conventional" αβT cells but also of inflammatory "innate" γδT cells.Entities:
Keywords: IL‐17; thymic epithelial cell; thymus; β5t; γδT
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Year: 2015 PMID: 25770130 PMCID: PMC4428049 DOI: 10.15252/embr.201540096
Source DB: PubMed Journal: EMBO Rep ISSN: 1469-221X Impact factor: 8.807