Takahashi Masanori, Osumi Noriko
Department of Developmental Neurobiology, Tohoku University Graduate School of Medicine, 2-1, Seiryo-machi, Aoba-ku, Sendai 980-8575, Japan.
Development. 2002 Mar;129(6):1327-38. doi: 10.1242/dev.129.6.1327.
Recent studies have shown that generation of different kinds of neurones is controlled by combinatorial actions of homeodomain (HD) proteins expressed in the neuronal progenitors. Pax6 is a HD protein that has previously been shown to be involved in the differentiation of the hindbrain somatic (SM) motoneurones and V1 interneurones in the hindbrain and/or spinal cord. To investigate in greater depth the role of Pax6 in generation of the ventral neurones, we first examined the expression patterns of HD protein genes and subtype-specific neuronal markers in the hindbrain of the Pax6 homozygous mutant rat. We found that Islet2 (SM neurone marker) and En1 (V1 interneurone marker) were transiently expressed in a small number of cells, indicating that Pax6 is not directly required for specification of these neurones. We also observed that domains of all other HD protein genes (Nkx2.2, Nkx6.1, Irx3, Dbx2 and Dbx1) were shifted and their boundaries became blurred. Thus, Pax6 is required for establishment of the progenitor domains of the ventral neurones. Next, we performed Pax6 overexpression experiments by electroporating rat embryos in whole embryo culture. Pax6 overexpression in the wild type decreased expression of Nkx2.2, but ectopically increased expression of Irx3, Dbx1 and Dbx2. Moreover, electroporation of Pax6 into the Pax6 mutant hindbrain rescued the development of Islet2-positive and En1-positive neurones. To know reasons for perturbed progenitor domain formation in Pax6 mutant, we examined expression patterns of Shh signalling molecules and states of cell death and cell proliferation. Shh was similarly expressed in the floor plate of the mutant hindbrain, while the expressions of Ptc1, Gli1 and Gli2 were altered only in the progenitor domains for the motoneurones. The position and number of TUNEL-positive cells were unchanged in the Pax6 mutant. Although the proportion of cells that were BrdU-positive slightly increased in the mutant, there was no relationship with specific progenitor domains. Taken together, we conclude that Pax6 regulates specification of the ventral neurone subtypes by establishing the correct progenitor domains.
最近的研究表明,不同类型神经元的生成受神经祖细胞中表达的同源结构域(HD)蛋白的组合作用控制。Pax6是一种HD蛋白,先前已证明其参与后脑躯体(SM)运动神经元以及后脑和/或脊髓中V1中间神经元的分化。为了更深入地研究Pax6在腹侧神经元生成中的作用,我们首先检查了Pax6纯合突变大鼠后脑HD蛋白基因和亚型特异性神经元标志物的表达模式。我们发现Islet2(SM神经元标志物)和En1(V1中间神经元标志物)在少数细胞中短暂表达,这表明这些神经元的特化并不直接需要Pax6。我们还观察到所有其他HD蛋白基因(Nkx2.2、Nkx6.1、Irx3、Dbx2和Dbx1)的结构域发生了移位,其边界变得模糊。因此,腹侧神经元祖细胞结构域的建立需要Pax6。接下来,我们通过在全胚胎培养中对大鼠胚胎进行电穿孔来进行Pax6过表达实验。野生型中Pax6过表达会降低Nkx2.2的表达,但会异位增加Irx3、Dbx1和Dbx2的表达。此外,将Pax6电穿孔到Pax6突变体后脑可挽救Islet2阳性和En1阳性神经元的发育。为了了解Pax6突变体中祖细胞结构域形成受到干扰的原因,我们检查了Shh信号分子的表达模式以及细胞死亡和细胞增殖状态。Shh在突变体后脑的底板中表达相似,而Ptc1、Gli1和Gli2的表达仅在运动神经元的祖细胞结构域中发生改变。Pax6突变体中TUNEL阳性细胞的位置和数量没有变化。虽然突变体中BrdU阳性细胞的比例略有增加,但与特定的祖细胞结构域没有关系。综上所述,我们得出结论,Pax6通过建立正确的祖细胞结构域来调节腹侧神经元亚型的特化。