Weichhart Thomas, Hengstschläger Markus, Linke Monika
Medical University of Vienna, Institute of Medical Genetics, Währingerstrasse 10, 1090 Vienna, Austria.
Nat Rev Immunol. 2015 Oct;15(10):599-614. doi: 10.1038/nri3901.
The innate immune system is central for the maintenance of tissue homeostasis and quickly responds to local or systemic perturbations by pathogenic or sterile insults. This rapid response must be metabolically supported to allow cell migration and proliferation and to enable efficient production of cytokines and lipid mediators. This Review focuses on the role of mammalian target of rapamycin (mTOR) in controlling and shaping the effector responses of innate immune cells. mTOR reconfigures cellular metabolism and regulates translation, cytokine responses, antigen presentation, macrophage polarization and cell migration. The mTOR network emerges as an integrative rheostat that couples cellular activation to the environmental and intracellular nutritional status to dictate and optimize the inflammatory response. A detailed understanding of how mTOR metabolically coordinates effector responses by myeloid cells will provide important insights into immunity in health and disease.
先天性免疫系统对于维持组织稳态至关重要,并且能通过病原体或无菌性损伤对局部或全身的干扰迅速做出反应。这种快速反应必须得到代谢支持,以允许细胞迁移和增殖,并实现细胞因子和脂质介质的高效产生。本综述聚焦于雷帕霉素哺乳动物靶点(mTOR)在控制和塑造先天性免疫细胞效应反应中的作用。mTOR重塑细胞代谢并调节翻译、细胞因子反应、抗原呈递、巨噬细胞极化和细胞迁移。mTOR网络作为一个整合变阻器出现,它将细胞激活与环境和细胞内营养状态联系起来,以决定和优化炎症反应。深入了解mTOR如何在代谢上协调髓系细胞的效应反应,将为健康和疾病中的免疫提供重要见解。