Yamada Mayumi, Terao Mami, Terashima Toshio, Fujiyama Tomoyuki, Kawaguchi Yoshiya, Nabeshima Yo-ichi, Hoshino Mikio
Department of Pathology and Tumor Biology, Kyoto University Graduate School of Medicine, Sakyo-ku, Kyoto 606-8501, Japan.
J Neurosci. 2007 Oct 10;27(41):10924-34. doi: 10.1523/JNEUROSCI.1423-07.2007.
Climbing fiber (CF) neurons in the inferior olivary nucleus (ION) extend their axons to Purkinje cells, playing a crucial role in regulating cerebellar function. However, little is known about their precise place of birth and developmental molecular machinery. Here, we describe the origin of the CF neuron lineage and the involvement of Ptf1a (pancreatic transcription factor 1a) in CF neuron development. Ptf1a protein was found to be expressed in a discrete dorsolateral region of the embryonic caudal hindbrain neuroepithelium. Because expression of Ptf1a is not overlapping other transcription factors such as Math1 (mouse atonal homolog 1) and Neurogenin1, which are suggested to define domains within caudal hindbrain neuroepithelium (Landsberg et al., 2005), we named the neuroepithelial region the Ptf1a domain. Analysis of mice that express beta-galactosidase from the Ptf1a locus revealed that CF neurons are derived from the Ptf1a domain. In contrast, retrograde labeling of precerebellar neurons indicated that mossy fiber neurons are not derived from Ptf1a-expressing progenitors. We could observe a detailed migratory path of CF neurons from the Ptf1a domain to the ION during embryogenesis. In Ptf1a null mutants, putative immature CF neurons produced from this domain were unable to migrate or differentiate appropriately, resulting in a failure of ION formation. Apoptotic cells were observed in the mutant hindbrain. Furthermore, the fate of some cells in the Ptf1a lineage were changed to mossy fiber neurons in Ptf1a null mutants. These findings clarify the precise origin of CF neurons and suggest that Ptf1a controls their fate, survival, differentiation, and migration during development.
下橄榄核(ION)中的攀缘纤维(CF)神经元将其轴突延伸至浦肯野细胞,在调节小脑功能中起关键作用。然而,关于它们的确切诞生位置和发育分子机制却知之甚少。在此,我们描述了CF神经元谱系的起源以及胰腺转录因子1a(Ptf1a)在CF神经元发育中的作用。发现Ptf1a蛋白在胚胎尾侧后脑神经上皮的一个离散背外侧区域表达。由于Ptf1a的表达不与其他转录因子如Math1(小鼠无调性同源物1)和神经生成素1重叠,而这些转录因子被认为可定义尾侧后脑神经上皮内的区域(Landsberg等人,2005年),我们将该神经上皮区域命名为Ptf1a结构域。对从Ptf1a基因座表达β - 半乳糖苷酶的小鼠的分析表明,CF神经元源自Ptf1a结构域。相比之下,小脑前神经元的逆行标记表明苔藓纤维神经元并非源自表达Ptf1a的祖细胞。我们能够观察到胚胎发育过程中CF神经元从Ptf1a结构域到ION的详细迁移路径。在Ptf1a基因敲除突变体中,从该结构域产生的假定未成熟CF神经元无法正常迁移或分化,导致ION形成失败。在突变体后脑中观察到凋亡细胞。此外,在Ptf1a基因敲除突变体中,Ptf1a谱系中一些细胞的命运转变为苔藓纤维神经元。这些发现阐明了CF神经元的确切起源,并表明Ptf1a在发育过程中控制它们的命运、存活、分化和迁移。