TSC1/2 Signaling Complex Is Essential for Peripheral Naïve CD8+ T Cell Survival and Homeostasis in Mice
Author(s) -
Lianjun Zhang,
Hongbing Zhang,
Lanlan Li,
Yi Xiao,
Enyu Rao,
Zhuang Miao,
Hui Chen,
Lina Sun,
Hongran Li,
Guangwei Liu,
Yong Zhao
Publication year - 2012
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0030592
Subject(s) - pi3k/akt/mtor pathway , t cell , microbiology and biotechnology , cd8 , protein kinase b , biology , naive t cell , tsc1 , regulatory t cell , il 2 receptor , phosphorylation , cancer research , signal transduction , t cell receptor , immunology , immune system
The PI3K-Akt-mTOR pathway plays crucial roles in regulating both innate and adaptive immunity. However, the role of TSC1, a critical negative regulator of mTOR, in peripheral T cell homeostasis remains elusive. With T cell-specific Tsc1 conditional knockout (Tsc1 KO) mice, we found that peripheral naïve CD8 + T cells but not CD4 + T cells were severely reduced. Tsc1 KO naïve CD8 + T cells showed profound survival defect in an adoptive transfer model and in culture with either stimulation of IL-7 or IL-15, despite comparable CD122 and CD127 expression between control and KO CD8 + T cells. IL-7 stimulated phosphorylation of Akt(S473) was diminished in Tsc1 KO naïve CD8 + T cells due to hyperactive mTOR-mediated feedback suppression on PI3K-AKT signaling. Furthermore, impaired Foxo1/Foxo3a phosphorylation and increased pro-apoptotic Bim expression in Tsc1 KO naïve CD8 + T cells were observed upon stimulation of IL-7. Collectively, our study suggests that TSC1 plays an essential role in regulating peripheral naïve CD8 + T cell homeostasis, possible via an mTOR-Akt-FoxO-Bim signaling pathway.
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