Yamano T, Shimada M, Kawasaki H, Onaga A, Nishimura M
Acta Neuropathol. 1987;72(3):256-60. doi: 10.1007/BF00691098.
The macular mutant mouse was clinically and pathologically examined. The hemizygotes began to show white fur color and curly whiskers around postnatal day 3, then seizures and ataxia around day 8, while the normal littermates did not. The hemizygotes also increased weight gradually from birth to day 9, but then showed weight loss and died around day 15 with severe emaciation. These clinical features resembled those in Menkes kinky hair disease. There were no pathological changes in the cerebral cortex in the hemizygotes on day 7. On day 10, two to three clear vacuoles began to appear in a few neurons in the cerebrum. These neurons with vacuoles increased gradually in number and degenerative neurons were also observed by day 14. Ultrastructurally, they corresponded to giant abnormal mitochondria with an electron-lucent matrix and short peripherally located cristae. Other abnormal mitochondria, which were characterized by an electron-dense matrix with tubular or vesicular cristae, were also observed in the cerebral cortical neurons.
对黄斑突变小鼠进行了临床和病理检查。半合子在出生后第3天左右开始出现白色皮毛和卷曲的胡须,然后在第8天左右出现癫痫发作和共济失调,而正常同窝小鼠则没有这些症状。半合子从出生到第9天体重也逐渐增加,但随后体重减轻,并在第15天左右因严重消瘦而死亡。这些临床特征与门克斯卷发综合征相似。在第7天,半合子的大脑皮质没有病理变化。在第10天,大脑中的一些神经元开始出现两到三个清晰的空泡。到第14天,这些有空泡的神经元数量逐渐增加,同时也观察到了变性神经元。在超微结构上,它们对应于巨大的异常线粒体,其基质电子密度低,嵴位于周边且较短。在大脑皮质神经元中还观察到其他异常线粒体,其特征是基质电子密度高,嵴呈管状或泡状。