State Key Laboratory of Medical Neurobiology, Institutes of Brain Science, MOE Frontier Research Center for Brain Science, Department of Neurology, Zhongshan Hospital, Fudan University, Shanghai 200032, PR China.
Department of Molecular, Cell and Developmental Biology, University of California, Santa Cruz, CA 95064, USA.
Cereb Cortex. 2019 Dec 17;29(11):4831-4849. doi: 10.1093/cercor/bhz018.
Generation of olfactory bulb (OB) interneurons requires neural stem/progenitor cell specification, proliferation, differentiation, and young interneuron migration and maturation. Here, we show that the homeobox transcription factors Dlx1/2 are central and essential components in the transcriptional code for generating OB interneurons. In Dlx1/2 constitutive null mutants, the differentiation of GSX2+ and ASCL1+ neural stem/progenitor cells in the dorsal lateral ganglionic eminence is blocked, resulting in a failure of OB interneuron generation. In Dlx1/2 conditional mutants (hGFAP-Cre; Dlx1/2F/- mice), GSX2+ and ASCL1+ neural stem/progenitor cells in the postnatal subventricular zone also fail to differentiate into OB interneurons. In contrast, overexpression of Dlx1&2 in embryonic mouse cortex led to ectopic production of OB-like interneurons that expressed Gad1, Sp8, Sp9, Arx, Pbx3, Etv1, Tshz1, and Prokr2. Pax6 mutants generate cortical ectopia with OB-like interneurons, but do not do so in compound Pax6; Dlx1/2 mutants. We propose that DLX1/2 promote OB interneuron development mainly through activating the expression of Sp8/9, which further promote Tshz1 and Prokr2 expression. Based on this study, in combination with earlier ones, we propose a transcriptional network for the process of OB interneuron development.
嗅球(OB)中间神经元的产生需要神经干细胞/祖细胞的特化、增殖、分化以及年轻中间神经元的迁移和成熟。在这里,我们表明同源盒转录因子 Dlx1/2 是产生 OB 中间神经元的转录编码中的核心和必需组成部分。在 Dlx1/2 组成型缺失突变体中,背外侧神经节隆起中的 GSX2+ 和 ASCL1+神经干细胞/祖细胞的分化被阻断,导致 OB 中间神经元产生失败。在 Dlx1/2 条件性突变体(hGFAP-Cre; Dlx1/2F/- 小鼠)中,出生后室下区的 GSX2+ 和 ASCL1+神经干细胞/祖细胞也未能分化为 OB 中间神经元。相比之下,Dlx1&2 在胚胎小鼠皮层中的过表达导致了 OB 样中间神经元的异位产生,这些神经元表达 Gad1、Sp8、Sp9、Arx、Pbx3、Etv1、Tshz1 和 Prokr2。Pax6 突变体产生具有 OB 样中间神经元的皮层异位,但在复合 Pax6; Dlx1/2 突变体中不会发生这种情况。我们提出,DLX1/2 主要通过激活 Sp8/9 的表达来促进 OB 中间神经元的发育,这进一步促进了 Tshz1 和 Prokr2 的表达。基于这项研究,并结合早期的研究,我们提出了一个用于 OB 中间神经元发育过程的转录网络。