| Literature DB >> 27233961 |
Hong-Xia Wang1, Joyce S Cheng2, Shuai Chu1, Yu-Rong Qiu3, Xiao-Ping Zhong4.
Abstract
Thymic epithelial cells (TECs) play important roles in T cell generation. Mechanisms that control TEC development and function are still not well defined. The mammalian or mechanistic target of rapamycin complex (mTORC)2 signals to regulate cell survival, nutrient uptake, and metabolism. We report in the present study that mice with TEC-specific ablation of Rictor, a critical and unique adaptor molecule in mTORC2, display thymic atrophy, which accompanies decreased TEC numbers in the medulla. Moreover, generation of multiple T cell lineages, including conventional TCRαβ T cells, regulatory T cells, invariant NKT cells, and TCRγδ T cells, was reduced in TEC-specific Rictor-deficient mice. Our data demonstrate that mTORC2 in TECs is important for normal thymopoiesis and efficient T cell generation.Entities:
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Year: 2016 PMID: 27233961 PMCID: PMC4912958 DOI: 10.4049/jimmunol.1502698
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422