Hong Yu, Hiroshi Nishio, Joseph Barbi, Marisa Mitchell-Flack, Paolo D A Vignali, Ying Zheng, Andriana Lebid, Kwang-Yu Chang, Juan Fu, Makenzie Higgins, Ching-Tai Huang, Xuehong Zhang, Zhiguang Li, Lee Blosser, Ada Tam, Charles Drake, Drew Pardoll
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引用次数: 0
摘要
适应性 T 细胞反应伴随着 T 细胞电力和新陈代谢状态的不断重新布线。离子通道和营养物质转运体整合来自环境的生物电和生化信号,设定细胞的电和代谢状态。不同的电和代谢状态有助于 T 细胞免疫或耐受。在这里,我们以小鼠为研究对象,报告了神经营养素(Nrn1)通过调节调节性和效应性 T 细胞的功能来促进耐受性的发展。Nrn1 在调节性 T 细胞中的表达促进其扩增和抑制功能,而在 T 效应细胞中的表达则抑制其炎症反应。小鼠缺乏 Nrn1 会导致调节性 T 细胞和效应 T 细胞中的离子通道和营养物质转运体表达失调,导致不同的代谢结果,并影响自身免疫疾病的进展和恢复。这些发现确定了神经营养因子 Nrn1 的一种新的免疫功能,即以细胞环境依赖的方式调节 T 细胞代谢状态,并调节免疫反应的结果。
Neurotrophic factor Neuritin modulates T cell electrical and metabolic state for the balance of tolerance and immunity.
The adaptive T cell response is accompanied by continuous rewiring of the T cell's electric and metabolic state. Ion channels and nutrient transporters integrate bioelectric and biochemical signals from the environment, setting cellular electric and metabolic states. Divergent electric and metabolic states contribute to T cell immunity or tolerance. Here, we report in mice that neuritin (Nrn1) contributes to tolerance development by modulating regulatory and effector T cell function. Nrn1 expression in regulatory T cells promotes its expansion and suppression function, while expression in the T effector cell dampens its inflammatory response. Nrn1 deficiency in mice causes dysregulation of ion channel and nutrient transporter expression in Treg and effector T cells, resulting in divergent metabolic outcomes and impacting autoimmune disease progression and recovery. These findings identify a novel immune function of the neurotrophic factor Nrn1 in regulating the T cell metabolic state in a cell context-dependent manner and modulating the outcome of an immune response.
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