Takebayashi Hirohide, Nabeshima Yoko, Yoshida Shosei, Chisaka Osamu, Ikenaka Kazuhiro, Nabeshima Yo-ichi
Department of Pathology and Tumor Biology, Graduate School of Medicine, Kyoto University, Yoshida, Konoe-cho, Sakyo-ku, Japan.
Curr Biol. 2002 Jul 9;12(13):1157-63. doi: 10.1016/s0960-9822(02)00926-0.
Sonic hedgehog (Shh), an organizing signal from ventral midline structures, is essential for the induction and maintenance of many ventral cell types in the embryonic neural tube. Olig1 and Olig2 are related basic helix-loop-helix factors induced by Shh in the ventral neural tube. Although expression analyses and gain-of-function experiments suggested that these factors were involved in motoneuron and oligodendrocyte development, they do not clearly define the functional differences between Olig1 and Olig2. We generated mice with a homozygous inactivation of Olig2. These mice did not feed and died on the day of birth. In the spinal cord of the mutant mice, motoneurons are largely eliminated and oligodendrocytes are not produced. Olig2(-/-) neuroepithelial cells in the ventral spinal cord failed to differentiate into motoneurons or oligodendrocytes and expressed an astrocyte marker, S100beta, at the time of oligodendrogenesis. Olig1 or Olig3, other family members, were expressed in the descendent cells that should have expressed Olig2. We concluded that Olig2 is an essential transcriptional regulator in motoneuron and oligodendrocyte development. Our data provide the first evidence that a single gene mutation leads to the loss of two cell types, motoneuron and oligodendrocyte.
音猬因子(Shh)是一种来自腹侧中线结构的组织信号,对于胚胎神经管中多种腹侧细胞类型的诱导和维持至关重要。Olig1和Olig2是腹侧神经管中由Shh诱导产生的相关碱性螺旋-环-螺旋因子。尽管表达分析和功能获得实验表明这些因子参与运动神经元和少突胶质细胞的发育,但它们并未明确界定Olig1和Olig2之间的功能差异。我们构建了Olig2纯合失活的小鼠。这些小鼠无法进食,在出生当天死亡。在突变小鼠的脊髓中,运动神经元大量缺失,少突胶质细胞无法产生。腹侧脊髓中的Olig2(-/-)神经上皮细胞无法分化为运动神经元或少突胶质细胞,并且在少突胶质细胞生成时表达星形胶质细胞标志物S100β。Olig1或Olig3等其他家族成员在本应表达Olig2的后代细胞中表达。我们得出结论,Olig2是运动神经元和少突胶质细胞发育中必不可少的转录调节因子。我们的数据首次证明,单一基因突变会导致运动神经元和少突胶质细胞这两种细胞类型的缺失。