Authors: | Kim, J. S.; Sklarz, T.; Banks, L. B.; Gohil, M.; Waickman, A. T.; Skuli, N.; Krock, B. L.; Luo, C. T.; Hu, W.; Pollizzi, K. N.; Li, M. O.; Rathmell, J. C.; Birnbaum, M. J.; Powell, J. D.; Jordan, M. S.; Koretzky, G. A. |
Article Title: | Natural and inducible TH17 cells are regulated differently by Akt and mTOR pathways |
Abstract: | Natural T helper 17 (nTH17) cells are a population of interleukin 17 (IL-17)-producing cells that acquire effector function in the thymus during development. Here we demonstrate that the serine/threonine kinase Akt has a critical role in regulating nTH17 cell development. Although Akt and the downstream mTORC1-ARNT-HIFα axis were required for generation of inducible TH17 (iTH17) cells, nT H17 cells developed independently of mTORC1. In contrast, mTORC2 and inhibition of Foxo proteins were critical for development of nTH17 cells. Moreover, distinct isoforms of Akt controlled the generation of T H17 cell subsets, as deletion of Akt2, but not of Akt1, led to defective generation of iTH17 cells. These findings define mechanisms regulating nTH17 cell development and reveal previously unknown roles of Akt and mTOR in shaping subsets of T cells. © 2013 Nature America, Inc. All rights reserved. |
Keywords: | signal transduction; protein kinase b; s6 kinase; controlled study; protein expression; protein phosphorylation; nonhuman; flow cytometry; cd8+ t lymphocyte; animal cell; mouse; cell maturation; animal experiment; cd4+ t lymphocyte; cell subpopulation; interleukin 17; th17 cell; hypoxia inducible factor 1alpha; transcription factor foxo; protein kinase b beta; mammalian target of rapamycin complex 1; mammalian target of rapamycin complex 2 |
Journal Title: | Nature Immunology |
Volume: | 14 |
Issue: | 6 |
ISSN: | 1529-2908 |
Publisher: | Nature Publishing Group |
Date Published: | 2013-06-01 |
Start Page: | 611 |
End Page: | 618 |
Language: | English |
DOI: | 10.1038/ni.2607 |
PROVIDER: | scopus |
PUBMED: | 23644504 |
PMCID: | PMC3711189 |
DOI/URL: | |
Notes: | --- - "Export Date: 1 July 2013" - "CODEN: NIAMC" - "Source: Scopus" |