U I Walther, B Wilhelm, S C Walther, H Mückter, W Forth
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引用次数: 9
摘要
锌中毒与还原性谷胱甘肽(GSH)减少和氧化性谷胱甘肽(GSSG)含量增加有关,这可能是锌对GSSG还原酶的抑制所致。在这项研究中,我们通过薄层色谱法研究了锌在(35)s -半胱氨酸掺入后对不同肺细胞系GSH合成率的影响。本研究使用2个肺泡上皮细胞系(A549和L2)和2个人成纤维细胞样肺细胞系(11Lu和16Lu)。不同细胞系在15-200 μ m (L2, 11Lu)、3h (16Lu)和4h (A549)锌暴露于细胞后均能达到等效蛋白合成抑制。在A549细胞中,GSH耗竭和GSSG增加明显低于其他细胞系。在测试的细胞系中,半胱氨酸(Cys)掺入GSH的情况没有不同,而11Lu细胞暴露于锌后,仅在(35)S-Cys暴露1小时后新合成的GSH减少。与其他细胞系相比,只有11Lu细胞的Cys利用率明显降低。在所有细胞系中,Cys的可用性不受锌暴露的影响。锌介导的细胞谷胱甘肽耗竭后,没有发现谷胱甘肽合成率的补偿性增加。
Effect of zinc chloride on GSH synthesis rates in various lung cell lines.
Zinc toxicity has been linked to decreased reduced glutathione (GSH) and increased oxidized glutathione (GSSG) contents, which might be caused by a GSSG reductase inhibition by zinc. In this study we investigated zinc effects on GSH synthesis rates in various lung cell lines by thin-layer chromatography after (35)S-cysteine incorporation. Two alveolar epithelial cell lines (A549 and L2) and two human fibroblast-like lung cell lines (11Lu and 16Lu) were used in this study. Equipotent protein synthesis inhibition for the different cell lines was reached after 2 h (L2, 11Lu), 3 h (16Lu), and 4 h (A549) zinc exposure (15-200 microM) to cells. Here GSH depletion and GSSG increase in A549 cells were markedly lower than in the other cell lines tested. Incorporation of cysteine (Cys) into GSH was not different in the cell lines tested, while 11Lu cells only demonstrated a decrease of newly synthesized GSH after 1 h of (35)S-Cys exposure when cells were exposed to zinc. Only 11Lu cells showed a markedly decreased Cys availability as compared with the other cell lines. In all cell lines the availability of Cys was not affected by exposure to zinc. No compensating increase in GSH synthesis rates was found after zinc-mediated cellular GSH depletion.