Lancaster G A, Scriver C R
Pediatr Res. 1982 Jan;16(1):86-8. doi: 10.1203/00006450-198201001-00019.
We studied survival of normal (n=4) and cystinotic (n=3) fibroblast strains in selective (cystine-free) medium, with or without dithiothreitol (DTT)-thiol or disulfide. Cells were plated at low density first in maintenance medium (containing cystine), then washed and exposed to selective medium for 24 hr or longer. Cultures were trypsinized at specified times and the cells counted. Selective medium caused progressive detachment (greater than 90% by 72 hr) of control and cystinotic cells: DTT-disulfide (4 mM) and DTT-thiol (0.5 mM) both protected cystinotic cells (p less than 0.02) but not control cells in selective medium. DTT-thiol (0.5 mM) and DTT-disulfide (4mM) both depleted the intracellular non-protein cystine pool of cystinotic cells to less than 25 percent of pretreatment levels. Cystinotic cells preincubated with cysteamine (1 mM X 4 hr) to deplete the intracellular cystine pool were not protected by DTT-disulfide than with DTT-thiol. These findings imply that mobilization of intracellular cystine protects cystinotic cells in selective medium; cystinotic fibroblasts can utilize DTT-disulfide as well as DTT-thiol to mobilize cystine.
我们研究了正常(n = 4)和成胱氨酸尿症(n = 3)的成纤维细胞系在选择性(无胱氨酸)培养基中,添加或不添加二硫苏糖醇(DTT)-硫醇或二硫化物的情况下的存活情况。细胞首先以低密度接种于维持培养基(含胱氨酸)中,然后洗涤并暴露于选择性培养基中24小时或更长时间。在指定时间对培养物进行胰蛋白酶消化并计数细胞。选择性培养基导致对照细胞和成胱氨酸尿症细胞逐渐脱离(72小时时超过90%):DTT-二硫化物(4 mM)和DTT-硫醇(0.5 mM)在选择性培养基中均能保护成胱氨酸尿症细胞(p < 0.02),但不能保护对照细胞。DTT-硫醇(0.5 mM)和DTT-二硫化物(4 mM)均能使成胱氨酸尿症细胞内非蛋白胱氨酸池减少至预处理水平的25%以下。用半胱胺(1 mM×4小时)预孵育以耗尽细胞内胱氨酸池的成胱氨酸尿症细胞,与DTT-硫醇相比,DTT-二硫化物对其没有保护作用。这些发现表明,细胞内胱氨酸的动员可保护成胱氨酸尿症细胞在选择性培养基中存活;成胱氨酸尿症成纤维细胞可以利用DTT-二硫化物以及DTT-硫醇来动员胱氨酸。