鉴定驱动neurod1诱导的神经元重编程的核心调控程序。

IF 6.9 1区 生物学 Q1 CELL BIOLOGY Cell reports Pub Date : 2025-04-22 Epub Date: 2025-04-01 DOI:10.1016/j.celrep.2025.115523
Wen Li, Dan Su, Xining Li, Kang Lu, Qingpei Huang, Jiajun Zheng, Xiaopeng Luo, Gong Chen, Xiaoying Fan
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引用次数: 0

摘要

神经d1 (ND1)诱导的星形细胞到神经元(AtN)的转化有望治疗神经系统疾病。为了深入了解神经元重编程的分子机制,我们利用出生后大鼠皮层星形胶质细胞原代培养物建立了一个体外系统,并采用单细胞和多组学测序。我们的研究结果表明,最初的培养主要由未成熟的星形胶质细胞(ImAs)组成,可能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以获得成熟的神经元特征。我们发现ND1作为一个先锋因子,将星形细胞的染色质景观重塑为神经元的染色质景观。这种重组通过诱导H3K27ac修饰促进神经源性基因的表达。通过综合分析各种ND1诱导的神经元规范系统,我们确定了包括Hes6在内的25个ND1靶点作为关键调控因子。因此,我们的工作强调了ND1及其下游调节因子在神经元重编程中的关键作用。
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Identification of the core regulatory program driving NEUROD1-induced neuronal reprogramming.

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.

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来源期刊
Cell reports
Cell reports CELL BIOLOGY-
CiteScore
13.80
自引率
1.10%
发文量
1305
审稿时长
77 days
期刊介绍: Cell Reports publishes high-quality research across the life sciences and focuses on new biological insight as its primary criterion for publication. The journal offers three primary article types: Reports, which are shorter single-point articles, research articles, which are longer and provide deeper mechanistic insights, and resources, which highlight significant technical advances or major informational datasets that contribute to biological advances. Reviews covering recent literature in emerging and active fields are also accepted. The Cell Reports Portfolio includes gold open-access journals that cover life, medical, and physical sciences, and its mission is to make cutting-edge research and methodologies available to a wide readership. The journal's professional in-house editors work closely with authors, reviewers, and the scientific advisory board, which consists of current and future leaders in their respective fields. The advisory board guides the scope, content, and quality of the journal, but editorial decisions are independently made by the in-house scientific editors of Cell Reports.
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