Specific efflux of glutathione from the basolateral membrane domain in polarized MDCK cells during ricin-induced apoptosis

被引:29
|
作者
Oda, T [1 ]
Sadakata, N [1 ]
Komatsu, N [1 ]
Muramatsu, T [1 ]
机构
[1] Nagasaki Univ, Fac Fisheries, Div Biochem, Nagasaki 8528521, Japan
来源
JOURNAL OF BIOCHEMISTRY | 1999年 / 126卷 / 04期
关键词
apoptosis; caspases; GSH efflux; ricin; polarized MDCK cell;
D O I
10.1093/oxfordjournals.jbchem.a022508
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
Although the depletion of reduced glutathione (GSH) has been observed in a variety of apoptotic systems, little is known about the mechanism of GSH depletion. In this study we used polarized MDCK cells to study the GSH flux during ricin-induced apoptosis. Here we report that the specific accumulation of GSH occurred in the basolateral medium during ricin treatment with similar kinetics to in apoptotic changes such as an increase in caspase-3 like activity and DNA fragmentation, while there was no significant increase in the GSH level in apical medium. These results suggest that GSH efflux occurred through a GSH-specific channel or transporter located in the basolateral membrane domain of polarized MDCK cells undergoing apoptosis. Treatment with other protein toxins such as modeccin, Pseudomonas toxin, and diphtheria toxin, which can induce apoptotic cell death, also resulted in selective GSH efflux from the basolateral side, Thus, GSH efflux through a specific transporter may be a common step of apoptosis induced by these toxins, while these toxins have different intoxication mechanisms leading to protein synthesis inhibition. Pretreatment of cells with Z-Asp-CH2-DCB, a caspase family inhibitor, inhibited ricin-induced basolateral GSH efflux as well as DNA fragmentation, suggesting that the activation of caspases, i.e. those that are inhibited by Z-Asp-CH2-DCB, is implicated in the opening of the GSH transporter.
引用
收藏
页码:715 / 721
页数:7
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