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Association of TIM-3 expression with glucose metabolism in Jurkat T cells

机译:Jurkat T细胞中TIM-3表达与葡萄糖代谢的关系

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T cell activation is associated with increase in glycolysis and glutaminolysis. T cell immunoglobulin and mucin domain containing protein-3 (TIM-3), a T cell surface molecule, downregulates T cell activation and leads to insufficient immunity in cancer and chronic infection. TIM-3 regulates T cell activation possibly through alterations in metabolism; however, the relationship between TIM-3 expression and T cell metabolic changes has not been well studied. We investigated the association between TIM-3 expression and metabolic changes by analyzing glucose metabolism, glutamine metabolism, and mitochondrial function in TIM-3 overexpressing or knockout Jurkat T cell lines relative to their control cell lines. Glucose uptake and consumption, and lactate release were downregulated by TIM-3 expression but upregulated by TIM-3 knockout. Concomitantly, the expression of the glucose transporter, Glut1, but not Glut2, 3, or 4 was altered by TIM-3 expression. However, TIM-3 expression alone could not account for the change in glutamine consumption, glutamate release, and mitochondrial mass, ROS production or membrane potential in these cell lines. Our results show the association of TIM-3 expression with T cell glucose metabolism. These results are significant in chronic infections and cancers where it is necessary to control TIM-3 expressing T cells.
机译:T细胞活化与糖酵解和谷氨酸溶解的增加有关。 T细胞免疫球蛋白和含有蛋白-3(TIM-3)的粘膜结构域,T细胞表面分子下调T细胞活化并导致癌症和慢性感染的免疫力不足。 TIM-3可能通过新陈代谢的改变来调节T细胞活化;然而,蒂姆-3表达与T细胞代谢变化之间的关系尚未得到很好的研究。我们通过分析葡萄糖代谢,谷氨酰胺代谢和线粒体功能在TIM-3过表达或敲除JURKAT T细胞系相对于其对照细胞系来研究TIM-3表达和代谢改变之间的关联。通过Tim-3表达下调葡萄糖摄取和消耗,乳酸释放,但是通过TIM-3敲除上调。同时,通过TiM-3表达改变葡萄糖转运蛋白,葡萄糖转运蛋白,但不是Glut2,3或4的表达。然而,单独的Tim-3表达不能考虑这些细胞系中谷氨酰胺消耗,谷氨酸释放和线粒体质量,ROS产生或膜电位的变化。我们的结果表明,TIM-3表达与T细胞葡萄糖代谢的关系。这些结果在慢性感染和癌症中是显着的,其中有必要控制表达T细胞的TIM-3。

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