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培养的肾上腺皮质细胞中的硒缺乏:添加硒后谷胱甘肽过氧化物酶的恢复及对氢过氧化物的抗性

Selenium deficiency in cultured adrenocortical cells: restoration of glutathione peroxidase and resistance to hydroperoxides on addition of selenium.

作者信息

Hornsby P J, Pearson D W, Autor A P, Aldern K A, Harris S E

出版信息

J Cell Physiol. 1985 Apr;123(1):33-8. doi: 10.1002/jcp.1041230106.

Abstract

Cultured bovine adrenocortical cells were previously shown to be functionally deficient in selenium and vitamin E when grown in medium supplemented with fetal bovine serum. In the present experiments, the lack of significant bioavailable amounts of selenium in the medium was demonstrated by the finding of only low levels of glutathione peroxidase in the cultured cells (0.008 U/mg protein compared with 0.045 U/mg protein in fresh adrenocortical tissue). When 20 nM selenium as selenite was added to the cultured adrenocortical cells, glutathione peroxidase activity increased continuously over 72 h, with a total increase of about eightfold over this period. Over the same time-course, the highest concentration of cumene hydroperoxide tolerated by the cells without cell death increased progressively from 10 microM to 50 microM. Addition of 1 microM alpha-tocopherol also increased the amount of cumene hydroperoxide tolerated to 50 microM. Cell death was measured by cloning efficiency after removal of cumene hydroperoxide. Addition of either selenium or alpha-tocopherol had little effect on the growth rate of the cells over six passages, even when residual vitamin E was removed from the serum by extraction with ether and residual low molecular weight selenium compounds were removed by dialysis. It is concluded that combined deficiency of selenium and vitamin E, at least in the presence of other components of fetal bovine serum, has little effect on the ability of the cells to survive under normal conditions, as evidenced by continued long-term proliferation. However, the low levels of glutathione peroxidase resulting from selenium deficiency cause an increase susceptibility to peroxide-mediated toxicity. The combined deficiency of selenium and vitamin E impairs the ability of cells to survive under adverse conditions, as well as altering mitochondrial functions, as previously demonstrated.

摘要

先前的研究表明,在添加胎牛血清的培养基中培养的牛肾上腺皮质细胞在功能上缺乏硒和维生素E。在本实验中,通过在培养细胞中仅发现低水平的谷胱甘肽过氧化物酶(0.008 U/mg蛋白质,而新鲜肾上腺皮质组织中为0.045 U/mg蛋白质),证明培养基中缺乏大量可生物利用的硒。当向培养的肾上腺皮质细胞中添加20 nM亚硒酸盐形式的硒时,谷胱甘肽过氧化物酶活性在72小时内持续增加,在此期间总体增加约八倍。在相同的时间进程中,细胞在不发生细胞死亡的情况下所能耐受的最高过氧化氢异丙苯浓度从10 microM逐渐增加到50 microM。添加1 microMα-生育酚也将细胞对过氧化氢异丙苯的耐受量增加到50 microM。在去除过氧化氢异丙苯后,通过克隆效率来测定细胞死亡情况。即使通过乙醚萃取从血清中去除残留的维生素E,并通过透析去除残留的低分子量硒化合物,添加硒或α-生育酚对细胞在六个传代过程中的生长速率几乎没有影响。结论是,至少在存在胎牛血清其他成分的情况下,硒和维生素E的联合缺乏对细胞在正常条件下的存活能力影响很小,长期持续增殖就证明了这一点。然而,硒缺乏导致的低水平谷胱甘肽过氧化物酶会增加细胞对过氧化物介导的毒性的易感性。硒和维生素E的联合缺乏会损害细胞在不利条件下的存活能力,同时也会改变线粒体功能,正如先前所证明的那样。

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