Toohey J I
Biochem Cell Biol. 1986 Aug;64(8):758-65. doi: 10.1139/o86-103.
Several systems which generate persulfide sulfur promote in vitro proliferation of L1210 murine lymphoma cells. The systems include cysteine disulfides and pyridoxal, cystamine and diamine oxidase, beta-mercaptoalcohol disulfides and an alcohol dehydrogenase, and sulfide-treated proteins and a thiol. Persulfide sulfur is very unstable at pH near 7 and an essential feature of the growth-supporting systems is the ability to generate persulfide sulfur at a very low rate for long periods of time. Methyl disulfides (R--S--S--CH3) also support growth of L1210 cells and are more stable than persulfides (R--S--S--H). The requirement for these sulfur groups by L1210 cells may be related to the fact that these cells are defective in at least two enzymes of sulfur metabolism, cystathionase and 5'-methylthioadenosine phosphorylase. These findings provide the first evidence that persulfide sulfur may have a physiological role.
几种能生成过硫化物硫的系统可促进L1210小鼠淋巴瘤细胞的体外增殖。这些系统包括半胱氨酸二硫化物和吡哆醛、胱胺和二胺氧化酶、β-巯基乙醇二硫化物和一种乙醇脱氢酶,以及经硫化物处理的蛋白质和一种硫醇。过硫化物硫在pH接近7时非常不稳定,而支持生长的系统的一个基本特征是能够长时间以非常低的速率生成过硫化物硫。甲基二硫化物(R--S--S--CH3)也支持L1210细胞的生长,并且比过硫化物(R--S--S--H)更稳定。L1210细胞对这些硫基团的需求可能与以下事实有关:这些细胞在硫代谢的至少两种酶,即胱硫醚酶和5'-甲硫腺苷磷酸化酶方面存在缺陷。这些发现提供了过硫化物硫可能具有生理作用的首个证据。