Nakamura Harukazu, Katahira Tatsuya, Matsunaga Eiji, Sato Tatsuya
Department of Molecular Neurobiology, Graduate School of Life Sciences and Institute of Development, Aging and Cancer, Tohoku University, Seiryo-machi 4-1, Aoba-ku, Sendai 980-8575, Japan.
Brain Res Brain Res Rev. 2005 Sep;49(2):120-6. doi: 10.1016/j.brainresrev.2004.10.005. Epub 2005 Jan 21.
Classical transplantation studies showed that the isthmus has an organizing activity upon the tectum and cerebellum. Since Fgf8 is expressed in the isthmus and mimics functionally isthmic grafts, it is accepted that Fgf8 plays pivotal role in the isthmic organizing activity. The fate of brain vesicles is determined by the combinations of transcription factors. The neural tube region where Otx2, Pax2, and En1 are expressed early on acquires midbrain identity. Pax3/7 forces the midbrain to differentiate into tectum. En1/2, Pax2/5, and Fgf8 form a positive feedback loop for their expression, thus misexpression of one of these molecules turns on the loop and forces presumptive diencephalon to differentiate into tectum. The isthmic organizer signal, Fgf8, stabilizes or changes the expression of the transcription factors in mid/hindbrain region. A strong Fgf8 signal activates the Ras-ERK signaling pathway, which in turn activates Irx2 in a rostrodorsal part of the hindbrain, and forces this tissue to differentiate into cerebellum.
经典的移植研究表明,峡部对顶盖和小脑具有组织活性。由于Fgf8在峡部表达并在功能上模拟峡部移植,因此人们认为Fgf8在峡部组织活性中起关键作用。脑泡的命运由转录因子的组合决定。早期表达Otx2、Pax2和En1的神经管区域获得中脑身份。Pax3/7促使中脑分化为顶盖。En1/2、Pax2/5和Fgf8形成它们表达的正反馈回路,因此这些分子之一的错误表达会开启该回路,并促使假定的间脑分化为顶盖。峡部组织者信号Fgf8稳定或改变中脑/后脑区域转录因子的表达。强烈的Fgf8信号激活Ras-ERK信号通路,进而在后脑的前背侧部分激活Irx2,并促使该组织分化为小脑。