Decoding the crosstalk between mevalonate metabolism and T cell function

被引:7
作者
Kennewick, Kelly T. T. [1 ]
Bensinger, Steven J. J. [1 ,2 ]
机构
[1] Univ Calif Los Angeles, Dept Microbiol Immunol & Mol Genet, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Dept Mol & Med Pharmacol, Los Angeles, CA 90095 USA
关键词
cholesterol; isoprenoids; mevalonate pathway; statins; T cells; HMG-COA REDUCTASE; COENZYME-A REDUCTASE; ELEMENT-BINDING PROTEINS; LOW-DENSITY-LIPOPROTEIN; LEUCINE ZIPPER PROTEIN; CHOLESTEROL-SYNTHESIS; MULTIPLE-SCLEROSIS; STEROL SYNTHESIS; LIPID RAFTS; 3-HYDROXY-3-METHYLGLUTARYL-COA REDUCTASE;
D O I
10.1111/imr.13200
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The mevalonate pathway is an essential metabolic pathway in T cells regulating development, proliferation, survival, differentiation, and effector functions. The mevalonate pathway is a complex, branched pathway composed of many enzymes that ultimately generate cholesterol and nonsterol isoprenoids. T cells must tightly control metabolic flux through the branches of the mevalonate pathway to ensure sufficient isoprenoids and cholesterol are available to meet cellular demands. Unbalanced metabolite flux through the sterol or the nonsterol isoprenoid branch is metabolically inefficient and can have deleterious consequences for T cell fate and function. Accordingly, there is tight regulatory control over metabolic flux through the branches of this essential lipid synthetic pathway. In this review we provide an overview of how the branches of the mevalonate pathway are regulated in T cells and discuss our current understanding of the relationship between mevalonate metabolism, cholesterol homeostasis and T cell function.
引用
收藏
页码:71 / 94
页数:24
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