Erickson Anders W, Tan Henry, Hendrikse Liam D, Millman Jake, Thomson Zachary, Golser Joseph, Khan Omar, He Guanyi, Bach Kathleen, Mishra Arpit Suresh, Kopic Janja, Krsnik Zeljka, Encha-Razavi Ferechte, Petrilli Giulia, Guimiot Fabien, Silvestri Evelina, Aldinger Kimberly A, Taylor Michael D, Millen Kathleen J, Haldipur Parthiv
The Arthur and Sonia Labatt Brain Tumor Research Centre, The Hospital for Sick Children, Toronto, ON M5G0A4, Canada.
Developmental and Stem Cell Biology Program, The Hospital for Sick Children, Toronto, ON M5G0A4, Canada.
Proc Natl Acad Sci U S A. 2025 Apr 29;122(17):e2415425122. doi: 10.1073/pnas.2415425122. Epub 2025 Apr 18.
The cerebellar ventricular zone (VZ) is the primary source of progenitors that generate cerebellar GABAergic neurons, including Purkinje cells (PCs) and interneurons (INs). This study provides detailed characterization of human cerebellar GABAergic neurogenesis using transcriptomic and histopathological analyses and reveals conserved and unique features compared to rodents. We show that the sequential progression of neurogenesis is conserved and occurs before 8 postconception weeks. Notably, PC differentiation occurs in the outer subventricular zone (SVZ), a region absent in the mouse cerebellum. Human PCs are generated during a compact two-week period before the onset of cerebral cortex histogenesis. A subset of human PCs retain proliferative marker expression weeks after leaving the VZ, another feature not observed in rodents. Human PC maturation is protracted with an extensive migration and reorganization throughout development with dendritic arborization developing in late gestation. We define a continuous transcriptional cascade of PC development from neuroepithelial cells to mature PCs. In contrast, while human interneuronal progenitors are born beginning in early fetal development, they exhibit an even more protracted differentiation across late gestation and into postnatal ages. These findings show dynamic developmental process for human cerebellar GABAergic neurons and underscore the importance of the embryonic environment, with early disruptions having potentially significant impacts.
小脑室管膜区(VZ)是产生小脑γ-氨基丁酸能神经元(包括浦肯野细胞(PCs)和中间神经元(INs))的祖细胞的主要来源。本研究利用转录组学和组织病理学分析对人类小脑γ-氨基丁酸能神经发生进行了详细表征,并揭示了与啮齿动物相比保守和独特的特征。我们表明,神经发生的顺序进展是保守的,发生在受孕后8周之前。值得注意的是,PC分化发生在外侧脑室下区(SVZ),这是小鼠小脑中不存在的区域。人类PCs在大脑皮质组织发生开始前的紧凑两周内产生。一部分人类PCs在离开VZ数周后仍保留增殖标记物表达,这是在啮齿动物中未观察到的另一个特征。人类PC成熟过程漫长,在整个发育过程中经历广泛的迁移和重组,树突分支在妊娠晚期发育。我们定义了从神经上皮细胞到成熟PCs的连续PC发育转录级联。相比之下,虽然人类中间神经元祖细胞在胎儿发育早期就开始产生,但它们在妊娠晚期和出生后阶段表现出更加漫长的分化过程。这些发现显示了人类小脑γ-氨基丁酸能神经元的动态发育过程,并强调了胚胎环境的重要性,早期干扰可能产生重大影响。