The optic nerve of the macular mouse as a model of Menkes' disease was
examined by electron microscopy. Since hemizygote macular mice die at
14 or 15 days of age, they were treated with 50 mu g CuCl2 per 0.1 mi
distilled water at 7 days of age. The optic nerves of 1-month-old hem
izygote macular mice treated with copper showed hypomyelination and un
myelinated axons, while 1-month-old heterozygote macular mice had foca
l demyelination of axons. The number of myelinated axons in treated he
mizygotes and heterozygotes was statistically significantly lower than
that in the control littermates. Oligodendrocytes form myelin sheaths
. Since oligodendrocytes of the hemizygote macular mice may have lower
activities of cuproenzymes, such as cytochrome oxidase and superoxide
dismutase, hypomyelination is assumed to be caused by the dysfunction
of oligodendrocyte. (C) 1996 Academic Press Limited