Sukhbaatar Nyamdelger, Hengstschläger Markus, Weichhart Thomas
Medical University of Vienna, Institute of Medical Genetics, Währingerstrasse 10, 1090 Vienna, Austria.
Medical University of Vienna, Institute of Medical Genetics, Währingerstrasse 10, 1090 Vienna, Austria.
Trends Immunol. 2016 Nov;37(11):778-789. doi: 10.1016/j.it.2016.08.009. Epub 2016 Sep 7.
Dendritic cells (DCs) are essential antigen-presenting cells that sample the extra- and intracellular milieu to process antigens for the instruction of T cell responses. The mammalian target of rapamycin (mTOR) network senses environmental cues and is important for numerous cellular processes. This review discusses how DCs use mTOR complexes (mTORC1 and 2) to adapt their cellular metabolism, transcriptional responses, and translation machinery to control DC development, antigen processing, cytokine production, and T cell stimulation. We present a spatiotemporal model suggesting that the mTOR network integrates pattern recognition and growth factor receptor activation with nutritional information from the cell and surrounding tissue to support T cell stimulation and tolerance. mTOR develops into a central player that regulates DC differentiation and immune functions.
树突状细胞(DCs)是重要的抗原呈递细胞,可对细胞外和细胞内环境进行采样,以处理抗原从而指导T细胞反应。雷帕霉素哺乳动物靶蛋白(mTOR)网络可感知环境信号,对众多细胞过程都很重要。本综述讨论了DCs如何利用mTOR复合物(mTORC1和mTORC2)来调节其细胞代谢、转录反应和翻译机制,以控制DC的发育、抗原处理、细胞因子产生和T细胞刺激。我们提出了一个时空模型,表明mTOR网络将模式识别和生长因子受体激活与来自细胞和周围组织的营养信息整合在一起,以支持T细胞刺激和耐受性。mTOR成为调节DC分化和免疫功能的核心因素。