Carson M J, Behringer R R, Brinster R L, McMorris F A
Wistar Institute, Philadelphia, Pennsylvania 19104.
Neuron. 1993 Apr;10(4):729-40. doi: 10.1016/0896-6273(93)90173-o.
Insulin-like growth factor I (IGF-I) is a potent regulator of oligodendrocyte development and myelination in vitro, but its effect on myelination in vivo has never been tested directly. Therefore, we examined brain growth and myelination in a transgenic mouse line that overexpresses IGF-I. By postnatal day 55, when brain growth and myelination are essentially complete in normal mice, the brains of transgenic mice were 55% larger than those of controls owing to an increase in cell size and apparently in cell number. Most or all brain structures appeared to be affected. At the same time, total myelin content of the transgenic mice was 130% greater than that of controls. Oligodendrocyte number as a percentage of total cell number was not increased in the transgenic mouse brains; the increase in myelin content was primarily the result of an increase in myelin production per oligodendrocyte. These findings indicate that IGF-I is a potent inducer of brain growth and myelination in vivo.
胰岛素样生长因子I(IGF-I)在体外是少突胶质细胞发育和髓鞘形成的有效调节因子,但其对体内髓鞘形成的影响从未直接进行过测试。因此,我们研究了过度表达IGF-I的转基因小鼠品系的脑生长和髓鞘形成情况。到出生后第55天,此时正常小鼠的脑生长和髓鞘形成基本完成,转基因小鼠的脑比对照组大55%,这是由于细胞大小增加,且细胞数量明显增多。大多数或所有脑结构似乎都受到了影响。与此同时,转基因小鼠的总髓鞘含量比对照组高130%。在转基因小鼠脑中,少突胶质细胞数量占总细胞数量的百分比并未增加;髓鞘含量的增加主要是由于每个少突胶质细胞的髓鞘生成增加所致。这些发现表明,IGF-I是体内脑生长和髓鞘形成的有效诱导剂。