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DAPK1 (death associated protein kinase 1) mediates mTORC1 activation and antiviral activities in CD8+ T cells.


ABSTRACT: Mechanistic target of rapamycin complex 1 (mTORC1) regulates CD8+ T-cell differentiation and function. Despite the links between PI3K-AKT and mTORC1 activation in CD8+ T cells, the molecular mechanism underlying mTORC1 activation remains unclear. Here, we show that both the kinase activity and the death domain of DAPK1 are required for maximal mTOR activation and CD8+ T-cell function. We found that TCR-induced activation of calcineurin activates DAPK1, which subsequently interacts with TSC2 via its death domain and phosphorylates TSC2 to mediate mTORC1 activation. Furthermore, both the kinase domain and death domain of DAPK1 are required for CD8+ T-cell antiviral responses in an LCMV infection model. Together, our data reveal a novel mechanism of mTORC1 activation that mediates optimal CD8+ T-cell function and antiviral activity.

SUBMITTER: Wei Z 

PROVIDER: S-EPMC7852660 | biostudies-literature | 2021 Jan

REPOSITORIES: biostudies-literature

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DAPK1 (death associated protein kinase 1) mediates mTORC1 activation and antiviral activities in CD8<sup>+</sup> T cells.

Wei Zhengping Z   Li Pingfei P   He Ran R   Liu Huicheng H   Liu Na N   Xia Yu Y   Bi Guoyu G   Du Qiuyang Q   Xia Minghui M   Pei Lei L   Wang Jing J   Wang Guihua G   Tang Zhao-Hui ZH   Cheng Xiang X   Li Huabin H   Li Zhuoya Z   Ye Lilin L   Laurence Arian A   Lu Youming Y   Yang Xiang-Ping XP  

Cellular & molecular immunology 20190920 1


Mechanistic target of rapamycin complex 1 (mTORC1) regulates CD8<sup>+</sup> T-cell differentiation and function. Despite the links between PI3K-AKT and mTORC1 activation in CD8<sup>+</sup> T cells, the molecular mechanism underlying mTORC1 activation remains unclear. Here, we show that both the kinase activity and the death domain of DAPK1 are required for maximal mTOR activation and CD8<sup>+</sup> T-cell function. We found that TCR-induced activation of calcineurin activates DAPK1, which subs  ...[more]

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