Bannai S, Tsukeda H
J Biol Chem. 1979 May 10;254(9):3444-50.
The export of glutathione from cultured human diploid fibroblasts into the surrounding medium was found by isotopic labeling experiments using [35S]cystine and by enzymatic measurements. The major part of the glutathione exported from the cells was found in normal culture medium as mixed disulfide of glutathione and cysteine. Radioactivity of 35S, mostly derived from cellular glutathione, was mainly located in glutathione moiety, not in cysteine moiety, of the mixed disulfide. Export of free glutathione was found when cystine-free medium was used. It was, therefore, concluded that mixed disulfide of glutathione and cysteine was formed in the medium by exported glutathione and medium cystine via sulfhydryl-disulfide exchange reaction. Amount of total glutathione exported from the cells was measured by enzymatic method and it was found that more than 10% of normal cellular glutathione was exported within 2 h. Apparent concentration of glutathione in the medium after a day of culture reached 3 to 4 micrometer, which was comparable to that observed in normal plasma by the same enzymatic method.
通过使用[35S]胱氨酸的同位素标记实验和酶促测量,发现培养的人二倍体成纤维细胞中的谷胱甘肽会分泌到周围培养基中。从细胞中分泌出的谷胱甘肽的主要部分在正常培养基中以谷胱甘肽和半胱氨酸的混合二硫键形式存在。35S的放射性主要来源于细胞内的谷胱甘肽,主要位于混合二硫键的谷胱甘肽部分,而非半胱氨酸部分。当使用无胱氨酸培养基时,发现有游离谷胱甘肽的分泌。因此,可以得出结论,培养基中的谷胱甘肽和半胱氨酸的混合二硫键是由分泌出的谷胱甘肽与培养基中的胱氨酸通过巯基-二硫键交换反应形成的。通过酶促方法测量了从细胞中分泌出的总谷胱甘肽的量,发现在2小时内超过10%的正常细胞内谷胱甘肽被分泌出来。培养一天后,培养基中谷胱甘肽的表观浓度达到3至4微摩尔,这与通过相同酶促方法在正常血浆中观察到的浓度相当。