Instituto Cajal, CSIC, E-28002 Madrid, Spain.
J Comp Neurol. 2010 May 15;518(10):1814-24. doi: 10.1002/cne.22304.
Neurogenin 3 (Ngn3), a proneural gene controlled by the Notch receptor, is implicated in the control of dendrite morphology and synaptic plasticity of cultured hippocampal neurons. Here we report the localization and subcellular distribution of Ngn3 in the hippocampus in vivo and in neuronal cultures. In situ hybridization showed Ngn3 mRNA expression in the pyramidal layer and dentate gyrus of adult mouse hippocampus. Immunohistochemistry studies revealed that Ngn3 localization is mostly cytoplasmic in the hippocampal eminence at embryonic day (E)17 and postnatal day (P)0. At P10 it is cytoplasmic in CA1-CA3 pyramidal neurons and nuclear in granule cells of the dentate gyrus. In the adult hippocampus Ngn3 is localized in the nucleus and cytoplasm of both pyramidal neurons and granule cells. During development of cultured hippocampal neurons, Ngn3 mRNA expression is higher at stages of neuronal polarization, as judged by reverse-transcription polymerase chain reaction (RT-PCR), and it is mostly cytoplasmic. The tracking of the subcellular localization of Ngn3 in neurons infected with a virus expressing myc-Ngn3 suggests that the protein is quickly translocated to the cell nucleus after synthesis and then reexported to the cytoplasm. Treatment with leptomycin B, a potent and specific inhibitor of the exportin CRM1, induced its accumulation into the nucleus, suggesting that CRM1 mediates the nuclear export of Ngn3. These results suggest that Ngn3 may play a role in neuronal development by actions in the cytoplasm.
神经基因 3(Ngn3)是一种受 Notch 受体调控的神经前体细胞基因,与培养的海马神经元树突形态和突触可塑性的控制有关。在这里,我们报告了 Ngn3 在体内和神经元培养物中海马中的定位和亚细胞分布。原位杂交显示 Ngn3 mRNA 在成年小鼠海马的锥体层和齿状回中有表达。免疫组织化学研究表明,Ngn3 的定位在胚胎期 17 天(E17)和出生后 0 天(P0)的海马隆起中主要是细胞质。在 P10,它在 CA1-CA3 锥体神经元中是细胞质,在齿状回的颗粒细胞中是核质。在成年海马中,Ngn3 定位于锥体神经元和颗粒细胞的核质和细胞质中。在培养的海马神经元发育过程中,Ngn3 mRNA 的表达在神经元极化阶段更高,如逆转录聚合酶链反应(RT-PCR)判断,并且主要是细胞质。用表达 myc-Ngn3 的病毒感染神经元后,对 Ngn3 的亚细胞定位进行跟踪,表明该蛋白在合成后很快被转运到细胞核,然后再重新输出到细胞质。用莱普霉素 B 处理,一种有效的、特异性的 CRM1 出口抑制剂,诱导其在细胞核中积累,表明 CRM1 介导了 Ngn3 的核输出。这些结果表明,Ngn3 可能通过在细胞质中的作用在神经元发育中发挥作用。