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Loss of Suppressor of Fused in Mid-Corticogenesis Leads to the Expansion of Intermediate Progenitors

机译:在中皮层发生中融合抑制基因的丧失导致中间祖细胞的扩增

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摘要

Neural progenitors in the embryonic neocortex must be tightly regulated in order to generate the correct number and projection neuron subtypes necessary for the formation of functional neocortical circuits. In this study, we show that the intracellular protein Suppressor of Fused (Sufu) regulates the proliferation of intermediate progenitor (IP) cells at later stages of corticogenesis to affect the number of Cux1+ upper layer neurons in the postnatal neocortex. This correlates with abnormal levels of the repressor form of Gli3 (Gli3R) and the ectopic expression of Patched 1 (Ptch1), a Sonic Hedgehog (Shh) target gene. These studies reveal that the canonical role of Sufu as an inhibitor of Shh signaling is conserved at later stages of corticogenesis and that Sufu plays a crucial role in regulating neuronal number by controlling the cell cycle dynamics of IP cells in the embryonic neocortex.
机译:必须严格调节胚胎新皮层中的神经祖细胞,以产生形成功能性新皮层回路所需的正确数目和投射神经元亚型。在这项研究中,我们表明融合蛋白(Sufu)的细胞内蛋白抑制因子在皮质形成的后期阶段调节中间祖细胞(IP)的增殖,从而影响产后新皮层中Cux1 +上层神经元的数量。这与Gli3(Gli3R)阻遏物形式的异常水平和Sonic Hedgehog(Shh)靶基因Patched 1(Ptch1)的异位表达有关。这些研究表明,Sufu作为Shh信号抑制剂的规范作用在皮质发生的后期阶段是保守的,并且Sufu通过控制胚胎新皮层中IP细胞的细胞周期动态,在调节神经元数量中起关键作用。

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