Nagara H, Yajima K, Suzuki K
Acta Neuropathol. 1980;52(1):41-50. doi: 10.1007/BF00687227.
Chronological morphological alterations of the cerebellum, with particular attention to the Purkinje cells, were investigated in the brindled mottled MObr mouse, a neurological mutant mouse with close clinical similarity to Kinky hair syndrome (KHS) in humans. Seven days post-natally, slight irregularity in the morphology of mitochondria of the Purkinje cell perikarya was the only significant difference between hemizygous MObr mice and litter mate controls. With advancing age the mitochondrial change became more pronounced gradually in the former, not only in the perikarya but also in the dendrites. However, by day 31 or later the mitochondrial change subsided gradually and by day 91, the mitochondria in the majority of Purkinje cells became indistinguishable from those of littermate controls. Despite the extensive mitochondrial alteration, degeneration and necrosis of Purkinje cells were rather mild. Degeneration of white matter was quite conspicuous in the mutant mouse older than 31 days. These morphological changes of the cerebellum are compared with those of other neurological mutant mice, Nervous and Purkinje cell degeneration, and with KHS in humans.
在斑驳小鼠(MObr)中研究了小脑的时间顺序形态学改变,特别关注浦肯野细胞。斑驳小鼠是一种神经突变小鼠,在临床上与人类的卷曲毛发综合征(KHS)极为相似。出生后7天,半合子MObr小鼠与同窝对照小鼠之间唯一显著的差异是浦肯野细胞胞体线粒体形态略有不规则。随着年龄的增长,前者的线粒体变化逐渐变得更加明显,不仅在胞体中,而且在树突中也是如此。然而,到31天或更晚时,线粒体变化逐渐消退,到91天时,大多数浦肯野细胞中的线粒体与同窝对照小鼠的线粒体已无法区分。尽管线粒体发生了广泛改变,但浦肯野细胞的变性和坏死相当轻微。在31天以上的突变小鼠中,白质变性非常明显。将小脑的这些形态学变化与其他神经突变小鼠、神经和浦肯野细胞变性以及人类的KHS的变化进行了比较。