Robbins J H, Scudiero D A, Otsuka F, Tarone R E, Brumback R A, Wirtschafter J D, Polinsky R J, Barrett S F, Moshell A N, Scarpinato R G
J Neurol Neurosurg Psychiatry. 1984 Apr;47(4):391-8. doi: 10.1136/jnnp.47.4.391.
Lymphoblastoid lines from nine Usher's syndrome (recessively inherited retinitis pigmentosa and congenital sensorineural deafness) patients (representing eight kindreds) and from ten Duchenne muscular dystrophy patients (representing seven kindreds) showed a small but statistically significant hypersensitivity to the lethal effects of X-rays, as measured by the cellular ability to exclude the vital dye trypan blue, when compared with lines from 26 normal control subjects. Fibroblast lines from the Usher's syndrome patients, treated with X-rays or the radiomimetic, DNA-damaging chemical N-methyl-N'-nitro-N-nitrosoguanidine, also showed a statistically significant hypersensitivity when compared to normal fibroblast lines. These findings are consistent with the possibility that defective DNA repair mechanisms may be involved in the pathogenesis of these degenerative diseases.
来自9名Usher综合征(隐性遗传性色素性视网膜炎和先天性感音神经性耳聋)患者(代表8个家族)和10名杜兴氏肌营养不良患者(代表7个家族)的淋巴母细胞系,与来自26名正常对照受试者的细胞系相比,通过细胞排除活性染料台盼蓝的能力测定,显示出对X射线致死效应有轻微但具有统计学意义的超敏反应。与正常成纤维细胞系相比,用X射线或拟放射性、DNA损伤化学物质N-甲基-N'-硝基-N-亚硝基胍处理的Usher综合征患者的成纤维细胞系也显示出具有统计学意义的超敏反应。这些发现与DNA修复机制缺陷可能参与这些退行性疾病发病机制的可能性一致。