分解代谢
化学
T细胞
酶
新陈代谢
蛋白质亚单位
细胞
生物化学
细胞代谢
氨基酸
功能(生物学)
代谢中间体
细胞生物学
生物
免疫系统
基因
免疫学
作者
Eleanor Minogue,Pedro P. Cunha,Brennan J. Wadsworth,Guinevere L. Grice,Shiv K. Sah‐Teli,R. J. F. Hughes,David Bargiela,Alessandro Quaranta,Javier Zurita,Robin Antrobus,Pedro Veliça,Laura Barbieri,Craig E. Wheelock,Peppi Koivunen,James A. Nathan,Iosifina P. Foskolou,Randall S. Johnson
标识
DOI:10.1038/s42255-023-00855-2
摘要
T cell function and fate can be influenced by several metabolites: in some cases, acting through enzymatic inhibition of α-ketoglutarate-dependent dioxygenases, in others, through post-translational modification of lysines in important targets. We show here that glutarate, a product of amino acid catabolism, has the capacity to do both, and has potent effects on T cell function and differentiation. We found that glutarate exerts those effects both through α-ketoglutarate-dependent dioxygenase inhibition, and through direct regulation of T cell metabolism via glutarylation of the pyruvate dehydrogenase E2 subunit. Administration of diethyl glutarate, a cell-permeable form of glutarate, alters CD8
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