McAlhaney W W, Banik N L, Greenfield S, Hogan E L
Neurochem Res. 1986 Feb;11(2):173-83. doi: 10.1007/BF00967966.
Six proteolytic enzymes were assayed for activity in quaking CNS in examining the hypothesis that increased proteolytic activity contributes to the hypomyelination characteristics of this mutant. Cathepsin B-like enzyme, cathepsin D, neutral proteinase, calcium-activated neutral proteinase, prolyl endopeptidase, and diaminopeptidase II were assayed in whole homogenate of brain or spinal cord and each was found to have activity similar to that in normal mice. These results do not support a relationship between proteolysis and the genetic defect and suggest that other factors should be investigated to delineate the pathogenesis of this mutant.
在检验蛋白水解活性增加导致该突变体髓鞘形成不足特征这一假说时,对六种蛋白水解酶在震颤小鼠中枢神经系统中的活性进行了测定。在脑或脊髓的全匀浆中检测了组织蛋白酶B样酶、组织蛋白酶D、中性蛋白酶、钙激活中性蛋白酶、脯氨酰内肽酶和二肽酶II,发现它们各自的活性与正常小鼠相似。这些结果不支持蛋白水解与该遗传缺陷之间存在关联,并表明应研究其他因素以阐明该突变体的发病机制。