mTORC1 and mTORC2 kinase signaling and glucose metabolism drive follicular helper T cell differentiation Journal Article


Authors: Zeng, H.; Cohen, S.; Guy, C.; Shrestha, S.; Neale, G.; Brown, S. A.; Cloer, C.; Kishton, R. J.; Gao, X.; Youngblood, B.; Do, M.; Li, M. O.; Locasale, J. W.; Rathmell, J. C.; Chi, H.
Article Title: mTORC1 and mTORC2 kinase signaling and glucose metabolism drive follicular helper T cell differentiation
Abstract: Follicular helper T (Tfh) cells are crucial for germinal center (GC) formation and humoral adaptive immunity. Mechanisms underlying Tfh cell differentiation in peripheral and mucosal lymphoid organs are incompletely understood. We report here that mTOR kinase complexes 1 and 2 (mTORC1 and mTORC2) are essential for Tfh cell differentiation and GC reaction under steady state and after antigen immunization and viral infection. Loss of mTORC1 and mTORC2 in T cells exerted distinct effects on Tfh cell signature gene expression, whereas increased mTOR activity promoted Tfh responses. Deficiency of mTORC2 impaired CD4+ T cell accumulation and immunoglobulin A production and aberrantly induced the transcription factor Foxo1. Mechanistically, the costimulatory molecule ICOS activated mTORC1 and mTORC2 to drive glycolysis and lipogenesis, and glucose transporter 1-mediated glucose metabolism promoted Tfh cell responses. Altogether, mTOR acts as a central node in Tfh cells by linking immune signals to anabolic metabolism and transcriptional activity. © 2016 Elsevier Inc.
Journal Title: Immunity
Volume: 45
Issue: 3
ISSN: 1074-7613
Publisher: Cell Press  
Date Published: 2016-09-20
Start Page: 540
End Page: 554
Language: English
DOI: 10.1016/j.immuni.2016.08.017
PROVIDER: scopus
PMCID: PMC5050556
PUBMED: 27637146
DOI/URL:
Notes: Article -- Export Date: 2 November 2016 -- Source: Scopus
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  1. Ming Li
    111 Li
  2. Mytrang   Do
    16 Do