Dimethyl Itaconate Is Not Metabolized into Itaconate Intracellularly

被引:87
作者
ElAzzouny, Mahmoud [1 ]
Tom, Christopher T. M. B. [2 ]
Evans, Charles R. [1 ]
Olson, Lori L. [4 ]
Tanga, Mary J. [4 ]
Gallagher, Katherine A. [3 ]
Martin, Brent R. [2 ]
Burant, Charles F. [1 ]
机构
[1] Univ Michigan, Dept Internal Med, Ann Arbor, MI 48105 USA
[2] Univ Michigan, Dept Chem, Ann Arbor, MI 48105 USA
[3] Univ Michigan, Dept Surg, Ann Arbor, MI 48105 USA
[4] SRI Int, Menlo Pk, CA 94025 USA
基金
美国国家卫生研究院;
关键词
SUCCINATE-DEHYDROGENASE; INFLAMMATORY MACROPHAGES; INSULIN-SECRETION; GLUCOSE; ACID; METABOLOMICS; IMMUNITY; GENE-1; CELLS; GPR91;
D O I
10.1074/jbc.C117.775270
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Itaconic acid is an important metabolite produced by macrophages after stimulation with LPS. The role of itaconate in the inflammatory cascade is unclear. Here we used [C-13] itaconate and dimethyl [C-13] itaconate ( DMI) to probe itaconate metabolism, and find that [C-13] DMI is not metabolized to itaconate. [C-13] Itaconate in the cell culture medium leads to elevated intracellular levels of unlabeled succinate, with no evidence of intracellular uptake. The goal of this study is to encourage the development of effective pro-drug strategies to increase the intracellular levels of itaconate, which will enable more conclusive analysis of its action on macrophages and other cell and tissue types.
引用
收藏
页码:4766 / 4769
页数:4
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