Mikoshiba K, Aoki E, Tsukada Y
Brain Res. 1980 Jun 16;192(1):195-204. doi: 10.1016/0006-8993(80)91019-7.
Shiverer is a recessive autosomal mutant characterized by the deficiency of the myelin in the central nervous system. 2',3'-Cyclic nucleotide 3'-phosphohydrolase (CNPase) activity of the various parts of the central nervous system from the Shiverer did not differ significantly from those of the control. The analysis of the protein profiles of the purified myelin from the Shiverer showed a greatly decreased proportion of proteolipid protein, and almost complete absence of small and large basic proteins, and intermediate protein. Woldgram protein accounted for a much larger percentage of the total myelin protein than is the case in myelin from the control. Proteolipid protein, small and large basic proteins, and intermediate protein were found to be undetectable or decreased in various parts of the central nervous system from the Shiverer. Morphological observation by optic and electron microscope showed that the myelination of the optic nerve was equally affected as the spinal cord.
颤抖鼠是一种隐性常染色体突变体,其特征是中枢神经系统中髓磷脂缺乏。颤抖鼠中枢神经系统各部分的2',3'-环核苷酸3'-磷酸水解酶(CNPase)活性与对照组相比无显著差异。对颤抖鼠纯化髓磷脂的蛋白质谱分析表明,蛋白脂蛋白的比例大幅下降,大小碱性蛋白和中间蛋白几乎完全缺失。沃尔德格拉姆蛋白在总髓磷脂蛋白中所占的百分比比对照组髓磷脂中的情况要大得多。在颤抖鼠中枢神经系统的各个部位,蛋白脂蛋白、大小碱性蛋白和中间蛋白均未检测到或减少。光学显微镜和电子显微镜的形态学观察表明,视神经的髓鞘形成与脊髓受到的影响相同。