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mTOR复合物对自然杀伤细胞发育的转录调控

Transcriptional Regulation of NK Cell Development by mTOR Complexes.

作者信息

Yang Chao, Malarkannan Subramaniam

机构信息

Laboratory of Molecular Immunology and Immunotherapy, Versiti Blood Research Institute, Milwaukee, WI, United States.

Department of Microbiology and Immunology, Medical College of Wisconsin, Milwaukee, WI, United States.

出版信息

Front Cell Dev Biol. 2020 Nov 10;8:566090. doi: 10.3389/fcell.2020.566090. eCollection 2020.

Abstract

The mechanistic target of Rapamycin (mTOR) is essential for multiple cellular processes. The unique roles of mTOR complex 1 (mTORC1) or mTOR2 in regulating immune functions are emerging. NK cells are the major lymphocyte subset of innate immunity, and their development and effector functions require metabolic reprogramming. Recent studies demonstrate that in NK cells, conditionally disrupting the formation of mTORC1 or mTOR complex 2 (mTORC2) alters their development significantly. Transcriptomic profiling of NK cells at the single-cell level demonstrates that mTORC1 was critical for the early developmental progression, while mTORC2 regulated the terminal maturation. In this review, we summarize the essential roles of mTOR complexes in NK development and functions.

摘要

雷帕霉素作用机制靶点(mTOR)对多种细胞过程至关重要。mTOR复合物1(mTORC1)或mTOR2在调节免疫功能中的独特作用正在显现。自然杀伤细胞(NK细胞)是固有免疫的主要淋巴细胞亚群,其发育和效应功能需要代谢重编程。最近的研究表明,在NK细胞中,有条件地破坏mTORC1或mTOR复合物2(mTORC2)的形成会显著改变其发育。单细胞水平的NK细胞转录组分析表明,mTORC1对早期发育进程至关重要,而mTORC2调节终末成熟。在本综述中,我们总结了mTOR复合物在NK细胞发育和功能中的重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb6b/7683515/a28b6bcefa37/fcell-08-566090-g001.jpg

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