Li Wen, Su Dan, Li Xining, Lu Kang, Huang Qingpei, Zheng Jiajun, Luo Xiaopeng, Chen Gong, Fan Xiaoying
Guangdong-HongKong-Macau Institute of CNS Regeneration (GHMICR), Jinan University, Guangzhou 510632, China; Key Laboratory of CNS Regeneration (Ministry of Education), Guangdong Key Laboratory of Non-Human Primate Research, GHM Institute of CNS Regeneration, Jinan University, Guangzhou 510632, China.
GMU-GIBH Joint School of Life Sciences, The Fifth Affiliated Hospital of Guangzhou Medical University, Guangzhou National Laboratory, Guangzhou Medical University, Guangzhou 510005, China; The Bioland Laboratory, Guangzhou 510700, China.
Cell Rep. 2025 Apr 22;44(4):115523. doi: 10.1016/j.celrep.2025.115523. Epub 2025 Apr 1.
NEUROD1 (ND1)-induced astrocyte-to-neuron (AtN) conversion shows promise for treating neurological disorders. To gain insight into the molecular mechanisms of neuronal reprogramming, we established an in vitro system using primary cortical astrocyte cultures from postnatal rats and employed single-cell and multiomics sequencing. Our findings indicate that the initial cultures primarily consisted of immature astrocytes (ImAs), with potentially a minor presence of radial glial cells. The ImAs initially went through an intermediate state, activating both astrocyte and neural progenitor genes. Subsequently, they mimic in vivo neurogenesis to acquire mature neuronal characteristics. We show that ND1 acted as a pioneer factor that reshapes the chromatin landscape of astrocytes to that of neurons. This restructuring promotes the expression of neurogenic genes via inducing H3K27ac modification. Through integrative analysis of various ND1-induced neuronal specification systems, we identified 25 ND1 targets, including Hes6, as key regulators. Thus, our work highlights the key role of ND1 and its downstream regulators in neuronal reprogramming.
神经分化1(NEUROD1,ND1)诱导的星形胶质细胞向神经元(AtN)转化在治疗神经疾病方面显示出前景。为深入了解神经元重编程的分子机制,我们利用新生大鼠的原代皮质星形胶质细胞培养建立了一个体外系统,并采用单细胞和多组学测序技术。我们的研究结果表明,最初的培养物主要由未成熟星形胶质细胞(ImAs)组成,可能还存在少量放射状胶质细胞。ImAs最初经历一个中间状态,激活星形胶质细胞和神经祖细胞基因。随后,它们模拟体内神经发生过程以获得成熟神经元特征。我们发现ND1作为先驱因子将星形胶质细胞的染色质景观重塑为神经元的染色质景观。这种重塑通过诱导H3K27ac修饰促进神经发生基因的表达。通过对各种ND1诱导的神经元特化系统的综合分析,我们确定了包括Hes6在内的25个ND1靶点为关键调节因子。因此,我们的工作突出了ND1及其下游调节因子在神经元重编程中的关键作用。