Wen Yue, He Ping, Huang Zongyao, Ding Chaoqiong, Zhang Ting, Zhang Lanxin, Zheng Jianan, Chen Mei, Chen Chong, Liu Yu, Wang Yuan, Zhang Yan
Department of Neurosurgery, State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University, Chengdu 610041, China.
Tianfu Jincheng Laboratory, Chengdu 610093, China.
J Neurosci. 2025 Jun 25;45(26):e2090242025. doi: 10.1523/JNEUROSCI.2090-24.2025.
Epigenetic mechanisms are crucial in the tightly regulated process of neurogenesis from radial glial cells (RGCs) to intermediate progenitor cells (IPCs) to neurons during embryonic brain development. Plant homeodomain (PHD) finger proteins as important epigenetic readers are implicated in development and diseases, yet their roles in embryonic neurogenesis remain largely unexplored. In this study, we found different PHD finger proteins are differentially expressed along the neurogenesis trajectory. Among them, we investigated the function of PHF23 using mouse models, which is highly expressed in RGCs and IPCs, but not in neurons. Our findings demonstrate that PHF23 is essential for proper neurogenesis, and knock-out (3-KO) results in cortical developmental defects due to differentiation blockade of RGCs. Mechanistically, PHF23 bind with HDAC2, inhibiting its deacetylation activity on the active histone mark H3K27ac, thereby promoting the expression of neuronal differentiation pathway genes such as and Overexpression of rescues the differentiation defects of 3-KO NSCs. These results establish PHF23 as a pivotal regulator of neurogenesis, indicating cell type-specific functions of PHD finger proteins.
表观遗传机制在胚胎脑发育过程中从放射状胶质细胞(RGCs)到中间祖细胞(IPCs)再到神经元的神经发生严格调控过程中至关重要。植物同源结构域(PHD)指蛋白作为重要的表观遗传识别蛋白与发育和疾病有关,但其在胚胎神经发生中的作用仍 largely未被探索。在本研究中,我们发现不同的PHD指蛋白沿神经发生轨迹差异表达。其中,我们使用小鼠模型研究了PHF23的功能,其在RGCs和IPCs中高表达,但在神经元中不表达。我们的研究结果表明,PHF23对正常神经发生至关重要,敲除(KO)会由于RGCs的分化阻滞导致皮质发育缺陷。机制上,PHF23与HDAC2结合,抑制其对活性组蛋白标记H3K27ac的去乙酰化活性,从而促进神经元分化途径基因如 和 的表达。 的过表达挽救了KO神经干细胞的分化缺陷。这些结果确立了PHF23作为神经发生的关键调节因子,表明PHD指蛋白的细胞类型特异性功能。