Biechl Daniela, Dorigo Alessandro, Köster Reinhard W, Grothe Benedikt, Wullimann Mario F
Division of Neurobiology, Department Biology II, Ludwig-Maximilians-Universität München Munich, Germany.
Institute of Zoology, Cellular and Molecular Neurobiology, Technische Universität Braunschweig Braunschweig, Germany.
Front Neuroanat. 2016 May 2;10:49. doi: 10.3389/fnana.2016.00049. eCollection 2016.
The secreted signaling factor Sonic Hedgehog (Shh) acts in the floor plate of the developing vertebrate CNS to promote motoneuron development. In addition, shh has dorsal expression domains in the amniote alar plate (i.e., in isocortex, superior colliculus, and cerebellum). For example, shh expressing Purkinje cells act in transit amplification of external granular layer (EGL) cells of the developing cerebellum. Our previous studies had indicated the presence of an EGL in anamniote zebrafish, but a possible role of shh in the zebrafish cerebellar plate remained elusive. Therefore, we used an existing zebrafish transgenic line Tg(2.4shha-ABC-GFP)sb15; Shkumatava et al., 2004) to show this gene activity and its cellular localization in the larval zebrafish brain. Clearly, GFP expressing cells occur in larval alar zebrafish brain domains, i.e., optic tectum and cerebellum. Analysis of critical cerebellar cell markers on this transgenic background and a PH3 assay for mitotic cells reveals that Purkinje cells and eurydendroid cells are completely non-overlapping postmitotic cell populations. Furthermore, shh-GFP cells never express Zebrin II or parvalbumin, nor calretinin. They are thus neither Purkinje cells nor calretinin positive migrating rhombic lip derived cells. The shh-GFP cells also never correspond to PH3 positive cells of the ventral cerebellar proliferative zone or the upper rhombic lip-derived EGL. From this marker analysis and the location of shh-GFP cells sandwiched between calretinin positive rhombic lip derived cells and parvalbumin positive Purkinje cells, we conclude that shh-GFP expressing cells qualify as previously reported olig2 positive eurydendroid cells, which are homologous to the amniote deep cerebellar nuclei. We confirm this using double transgenic progeny of shh-GFP and olig2-dsRed zebrafish. Thus, these zebrafish eurydendroid cells may have the same role in transit amplification as Purkinje cells do in amniotes.
分泌型信号因子音猬因子(Shh)在发育中的脊椎动物中枢神经系统的底板中发挥作用,以促进运动神经元的发育。此外,shh在羊膜动物翼板(即新皮质、上丘和小脑)中有背侧表达域。例如,表达shh的浦肯野细胞在发育中小脑的外颗粒层(EGL)细胞的过渡扩增中起作用。我们之前的研究表明无羊膜动物斑马鱼中存在EGL,但shh在斑马鱼小脑板中的可能作用仍然难以捉摸。因此,我们使用现有的斑马鱼转基因品系Tg(2.4shha-ABC-GFP)sb15(Shkumatava等人,2004年)来展示该基因在斑马鱼幼体脑中的活性及其细胞定位。显然,表达GFP的细胞出现在斑马鱼幼体翼板脑区,即视顶盖和小脑。对该转基因背景下关键小脑细胞标志物的分析以及对有丝分裂细胞的PH3检测表明,浦肯野细胞和多形核细胞是完全不重叠的有丝分裂后细胞群体。此外,shh-GFP细胞从不表达Zebrin II或小白蛋白,也不表达钙视网膜蛋白。因此,它们既不是浦肯野细胞,也不是钙视网膜蛋白阳性的源自菱唇的迁移细胞。shh-GFP细胞也从不对应于腹侧小脑增殖区或上菱唇衍生的EGL的PH3阳性细胞。通过这种标志物分析以及shh-GFP细胞夹在钙视网膜蛋白阳性的菱唇衍生细胞和小白蛋白阳性的浦肯野细胞之间的位置,我们得出结论,表达shh-GFP的细胞符合先前报道的olig2阳性多形核细胞,它们与羊膜动物的小脑深部核团同源。我们使用shh-GFP和olig2-dsRed斑马鱼的双转基因后代证实了这一点。因此,这些斑马鱼多形核细胞在过渡扩增中可能具有与羊膜动物浦肯野细胞相同的作用。