Kang Y J, Enger M D
Department of Zoology, Iowa State University, Ames 50011.
Toxicology. 1988 Jan;48(1):93-101. doi: 10.1016/0300-483x(88)90063-7.
Depletion of cellular glutathione (GSH) has been shown to sensitize A549-T27 human tumor cells to the cytotoxic effects of Cd2+. In this study the temporal and quantitative relationships between reduced cellular GSH levels and cadmium cytotoxic response in these cells were further investigated. Exposure of A549-T27 cells to 10 mM buthionine sulfoximine (BSO) for 8 h decreased their GSH level by 65%. This GSH level remained relatively constant for 8 h in the presence or absence of BSO, but recovered to 83% of the normal cellular level 24 h after removal of BSO. Exposure to 5 microM Cd2+ for 8 h did not significantly change cellular GSH levels. Pretreatment of the A549-T27 cells with 10 mM BSO for 8 h and subsequent exposure of the cells to Cd2+ for 10 days, with or without concurrent treatment of 10 mM BSO during the first 8 h of Cd2+ exposure, resulted in disappearance of the 5 microM Cd2+ threshold for cytotoxic response and reduction of the LC50 from 31 microM Cd2+ to 21 microM. Similar results were obtained when BSO pretreated cells were exposed to Cd2+ for 8 h. The threshold for cytotoxic response of 10 microM Cd2+ disappeared and the LC50 was reduced from 60 microM to 29 microM Cd2+ (with concurrent BSO treatment) and 30 microM (BSO pretreatment only). The results show that GSH plays an important role in early cellular protective responses to Cd2+.
细胞内谷胱甘肽(GSH)的耗竭已被证明会使A549 - T27人肿瘤细胞对Cd2 +的细胞毒性作用敏感。在本研究中,进一步研究了这些细胞中细胞内还原型GSH水平与镉细胞毒性反应之间的时间和定量关系。将A549 - T27细胞暴露于10 mM丁硫氨酸亚砜胺(BSO)8小时,其GSH水平降低了65%。无论有无BSO存在,该GSH水平在8小时内保持相对恒定,但在去除BSO后24小时恢复到正常细胞水平的83%。暴露于5 microM Cd2 + 8小时不会显著改变细胞GSH水平。用10 mM BSO预处理A549 - T27细胞8小时,随后将细胞暴露于Cd2 + 10天,在Cd2 +暴露的前8小时内有无同时给予10 mM BSO,均导致细胞毒性反应的5 microM Cd2 +阈值消失,半数致死浓度(LC50)从31 microM Cd2 +降至21 microM。当用BSO预处理的细胞暴露于Cd2 + 8小时时,也获得了类似的结果。10 microM Cd2 +的细胞毒性反应阈值消失,LC50从60 microM降至29 microM Cd2 +(同时进行BSO处理)和30 microM(仅进行BSO预处理)。结果表明,GSH在细胞对Cd2 +的早期保护反应中起重要作用。