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转录因子 Sp8 和 Sp9 协调调控嗅球中间神经元的发育。

Transcription Factors Sp8 and Sp9 Coordinately Regulate Olfactory Bulb Interneuron Development.

机构信息

Department of Translational Neuroscience, Shanghai Pudong Hospital, State Key Laboratory of Medical Neurobiology, Institutes of Brain Science, and Collaborative Innovation Center for Brain Science, Fudan University, Shanghai, China.

Department of Molecular, Cell and Developmental Biology, University of California, Santa Cruz, CA, USA.

出版信息

Cereb Cortex. 2018 Sep 1;28(9):3278-3294. doi: 10.1093/cercor/bhx199.

Abstract

Neural stem cells in the postnatal telencephalic ventricular-subventricular zone (V-SVZ) generate new interneurons, which migrate tangentially through the rostral migratory stream (RMS) into the olfactory bulb (OB). The Sp8 and Sp9 transcription factors are expressed in neuroblasts, as well as in the immature and mature interneurons in the V-SVZ-RMS-OB system. Here we show that Sp8 and Sp9 coordinately regulate OB interneuron development: although Sp9 null mutants show no major OB interneuron defect, conditional deletion of both Sp8 and Sp9 resulted in a much more severe reduction of OB interneuron number than that observed in the Sp8 conditional mutant mice, due to defects in neuronal differentiation, tangential and radial migration, and increased cell death in the V-SVZ-RMS-OB system. RNA-Seq and RNA in situ hybridization reveal that, in Sp8/Sp9 double mutant mice, but not in Sp8 or Sp9 single mutant mice, newly born neuroblasts in the V-SVZ-RMS-OB system fail to express Prokr2 and Tshz1 expression, genes with known roles in promoting OB interneuron differentiation and migration, and that are involved in human Kallmann syndrome.

摘要

出生后端脑脑室下区(V-SVZ)中的神经干细胞产生新的中间神经元,这些中间神经元通过腹侧迁移流(RMS)向嗅球(OB)迁移。Sp8 和 Sp9 转录因子在神经母细胞中表达,也在 V-SVZ-RMS-OB 系统中的未成熟和成熟中间神经元中表达。在这里,我们表明 Sp8 和 Sp9 共同调节 OB 中间神经元的发育:尽管 Sp9 缺失突变体没有明显的 OB 中间神经元缺陷,但 Sp8 和 Sp9 的条件缺失导致 OB 中间神经元数量的减少比 Sp8 条件性突变体小鼠观察到的更为严重,这是由于 V-SVZ-RMS-OB 系统中的神经元分化、切向和径向迁移缺陷以及细胞死亡增加所致。RNA-Seq 和 RNA 原位杂交显示,在 Sp8/Sp9 双突变体小鼠中,但不在 Sp8 或 Sp9 单突变体小鼠中,V-SVZ-RMS-OB 系统中的新生神经母细胞未能表达 Prokr2 和 Tshz1 表达,这些基因已知在促进 OB 中间神经元分化和迁移中发挥作用,并且与人类 Kallmann 综合征有关。

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