Kang Y J, Clapper J A, Enger M D
Department of Zoology, Iowa State University, Ames.
Cell Biol Toxicol. 1989 Nov;5(3):249-59. doi: 10.1007/BF01795354.
Glutathione (GSH) depletion sensitizes human lung carcinoma (A549-T27) cells to the cytotoxic effects of Cd++. The effects of GSH depletion on Cd++ accumulation and Cd++-induced metallothionein (MT) content were investigated to determine the possible role of these Cd++ responses in the sensitization process. Cellular GSH was depleted to 20% to 25% of control levels with buthionine sulfoximine (BSO), or diethyl maleate (DEM), respectively. Neither treatment significantly affected Cd++-induced accumulation of exogenous 35s-cysteine into intracellular MT in a dose-dependent fashion. The results indicate that neither enhanced Cd++ accumulation nor reduced MT synthesis plays a primary role in affecting enhanced Cd++ cytotoxicity in A549 cells with reduced GSH levels. Although BSO inhibition of GSH synthesis enhanced MT synthesis, it sensitized the cells to Cd++, which suggests an additive effect of GSH and MT in cadmium cytoprotection. This observation also raises the possibility that intracellular cysteine levels limit Cd++-induced MT accumulation rates.
谷胱甘肽(GSH)耗竭使人类肺癌(A549 - T27)细胞对Cd++的细胞毒性作用敏感。研究了GSH耗竭对Cd++积累和Cd++诱导的金属硫蛋白(MT)含量的影响,以确定这些Cd++反应在致敏过程中可能发挥的作用。用丁硫氨酸亚砜胺(BSO)或马来酸二乙酯(DEM)分别将细胞内GSH耗竭至对照水平的20%至25%。两种处理均未以剂量依赖方式显著影响Cd++诱导的外源35s - 半胱氨酸积累到细胞内MT中。结果表明,在GSH水平降低的A549细胞中,增强的Cd++积累或减少的MT合成在影响增强的Cd++细胞毒性方面均不发挥主要作用。尽管BSO抑制GSH合成增强了MT合成,但它使细胞对Cd++敏感,这表明GSH和MT在镉细胞保护中具有累加效应。这一观察结果还提出了细胞内半胱氨酸水平限制Cd++诱导的MT积累速率的可能性。