State Key Laboratory of Medical Neurobiology, Institutes of Brain Science, MOE Frontier Research Center for Brain Science, Department of Neurology, Zhongshan Hospital, Fudan University, 138 Yi Xue Yuan Road, Shanghai 200032, PR China.
State Key Laboratory of Medical Neurobiology, Institutes of Brain Science, MOE Frontier Research Center for Brain Science, Department of Neurology, Zhongshan Hospital, Fudan University, 138 Yi Xue Yuan Road, Shanghai 200032, PR China.
Exp Neurol. 2019 Dec;322:113055. doi: 10.1016/j.expneurol.2019.113055. Epub 2019 Sep 3.
The striatum, the major component of the basal ganglia, consists of the caudate-putamen, nucleus accumbens and olfactory tubercle. The striatal principal projection neurons are comprised of medium spiny neurons (MSNs) with two dopamine receptors: DRD1 (D1 MSNs) and DRD2 (D2 MSNs). In the present study, we demonstrate that Zfhx3 is strongly expressed in the boundary of the subventricular zone (SVZ)/mantle zone (MZ) of the lateral ganglionic eminence (LGE), and its expression in the striatum is downregulated during the first postnatal week. At the cellular level, Zfhx3 is selectively expressed in immature D1 MSNs. In Zfhx3 conditional knockouts, we observed an accumulation of progenitors in the LGE SVZ at E16.5 and P0, and an increase in apoptosis in the postnatal striatum. BrdU birthdating experiments revealed that late born D1 MSN production was compromised. Accordingly, we observed a significant reduction in the number of D1 MSNs, whereas the number of D2 MSNs remained unaffected in the striatum of Zfhx3 conditional knockouts at P11. We concluded that Zfhx3 plays a critical role in the differentiation and survival of late born D1 MSNs.
纹状体是基底神经节的主要组成部分,由尾状核-壳核、伏隔核和嗅结节组成。纹状体的主要投射神经元是中型棘突神经元(MSNs),具有两种多巴胺受体:DRD1(D1 MSNs)和 DRD2(D2 MSNs)。在本研究中,我们证明 Zfhx3 在侧神经节隆起(LGE)的室下区(SVZ)/边缘区(MZ)边界处强烈表达,其在纹状体中的表达在出生后第一周下调。在细胞水平上,Zfhx3 选择性地表达在不成熟的 D1 MSNs 中。在 Zfhx3 条件敲除小鼠中,我们观察到 E16.5 和 P0 时 LGE SVZ 中的祖细胞积累,以及出生后纹状体中的细胞凋亡增加。BrdU 标记实验表明,晚期出生的 D1 MSN 产生受到损害。因此,我们观察到 Zfhx3 条件敲除小鼠的纹状体中 D1 MSN 数量显著减少,而 D2 MSN 数量保持不变。我们得出结论,Zfhx3 在晚期出生的 D1 MSN 的分化和存活中发挥关键作用。