Crawhall J C, Oshima R G, Schneider J A
Pediatr Res. 1977 Jan;11(1 Pt 1):41-5.
The cystine content of cystinotic fibroblasts increases with the length of time in cultivation. Four of five cystinotic cell strains showed an increase in cystine content with increased passage number. Cystinotic fibroblasts did not increase in cell number after 3 days in dialyzed fetal bovine serum. However, their cystine content increased almost 2-fold on a per cell number basis. Cystinotic cells incubated in cystine-free medium lost approximately 50% of their free cystine over a period of 12 hr and subsequently remained at about this level for 12 additional hr. Treatment of cystinotic cells with 1.0 mM dithiothreitol in complete medium reduced their free cystine content to about 25% of the initial level in 5 hr. The free cystine remained at this level after incubation overnight incystine-free medium without dithiothreitol. When dithiothreitol is added in the presence of a cystine-free medium, even more free cystine is removed from cystinotic cells (90%), and the free cystine content remains at this low level for as long as 48 hr if the cells are kept in a cystine-free medium. Cystinotic cells depleted of more than 50% of their intracellular free cystine by incubation in cystine-free medium reaccumulate cystine rapidly after replacement of cystine-containing medium. When cystinotic cells were depleted of their free cystine by treatment with dithiothreitol in a cystine-free medium and were then replaced in complete medium the intracellular free cystine reaccumulated rapidly, regaining its initial value in about 4 hr. The intracellular free cystine content found after 10 hr in complete medium reflected the cystine content of the medium. Cells in medium containing 0.266 mM cystine reaccumulated almost 60% more cystine than cells in medium with 0.066 mM cystine. When cystinotic and normal control fibroblasts were incubated for 2, 4, and 24 hr in either [35S]methionine or [35S]cystathionine, no radioactivity was recovered as cystine, cysteine, or glutathionine.
胱氨酸病成纤维细胞的胱氨酸含量随培养时间的延长而增加。五个胱氨酸病细胞株中有四个显示随着传代次数的增加胱氨酸含量增加。在透析胎牛血清中培养3天后,胱氨酸病成纤维细胞的细胞数量没有增加。然而,以每个细胞数量为基础,它们的胱氨酸含量几乎增加了两倍。在无胱氨酸培养基中孵育的胱氨酸病细胞在12小时内失去了约50%的游离胱氨酸,随后在另外12小时内保持在该水平左右。在完全培养基中用1.0 mM二硫苏糖醇处理胱氨酸病细胞5小时后,其游离胱氨酸含量降至初始水平的约25%。在无胱氨酸且无二硫苏糖醇的培养基中过夜孵育后,游离胱氨酸保持在该水平。当在无胱氨酸培养基存在下添加二硫苏糖醇时,甚至更多的游离胱氨酸从胱氨酸病细胞中被去除(90%),并且如果细胞保持在无胱氨酸培养基中,游离胱氨酸含量可在长达48小时内保持在低水平。通过在无胱氨酸培养基中孵育使细胞内游离胱氨酸减少超过50%的胱氨酸病细胞,在更换含胱氨酸培养基后会迅速重新积累胱氨酸。当胱氨酸病细胞在无胱氨酸培养基中用二硫苏糖醇处理耗尽其游离胱氨酸,然后更换为完全培养基时,细胞内游离胱氨酸迅速重新积累,在约4小时内恢复到初始值。在完全培养基中培养10小时后发现的细胞内游离胱氨酸含量反映了培养基中的胱氨酸含量。在含有0.266 mM胱氨酸的培养基中的细胞比在含有0.066 mM胱氨酸的培养基中的细胞重新积累的胱氨酸多近60%。当胱氨酸病和正常对照成纤维细胞在[35S]甲硫氨酸或[35S]胱硫醚中孵育2、4和24小时时,未检测到作为胱氨酸、半胱氨酸或谷胱甘肽回收的放射性。