The ergothioneine transporter (ETT): substrates and locations, an inventory

被引:46
作者
Grundemann, Dirk [1 ,2 ]
Hartmann, Lea
Flogel, Svenja
机构
[1] Univ Cologne, Fac Med, Dept Pharmacol, Gleueler Str 24, D-50931 Cologne, Germany
[2] Univ Cologne, Univ Hosp Cologne, Gleueler Str 24, D-50931 Cologne, Germany
关键词
brain; ergothioneine transporter; erythrocytes; macrophages; mass spectrometry; monocytes; neutrophils; substrate profile; ORGANIC CATION TRANSPORTER; CELL LINE HCMEC/D3; CATION/CARNITINE TRANSPORTER; FUNCTIONAL EXPRESSION; TISSUE DISTRIBUTION; MESSENGER-RNA; OCTN1; SLC22A4; ANTIOXIDANT ERGOTHIONEINE; DRUG TRANSPORTER; GENES;
D O I
10.1002/1873-3468.14269
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
In all vertebrates including mammals, the ergothioneine transporter ETT (obsolete name OCTN1; human gene symbol SLC22A4) is a powerful and highly specific transporter for the uptake of ergothioneine (ET). ETT is not expressed ubiquitously and only cells with high ETT cell-surface levels can accumulate ET to high concentration. Without ETT, there is no uptake because the plasma membrane is essentially impermeable to this hydrophilic zwitterion. Here, we review the substrate specificity and localization of ETT, which is prominently expressed in neutrophils, monocytes/macrophages, and developing erythrocytes. Most sites of strong expression are conserved across species, but there are also major differences. In particular, we critically analyze the evidence for the expression of ETT in the brain as well as recent data suggesting that the transporter SLC22A15 may also transport ET. We conclude that, to date, ETT remains the only well-defined biomarker for intracellular ET activity. In humans, the ability to take up, distribute, and retain ET depends principally on this transporter.
引用
收藏
页码:1252 / 1269
页数:18
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