Histone Lysine Demethylase KDM5 Inhibitor CPI-455 Induces Astrocytogenesis in Neural Stem Cells

IF 4.1 3区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY ACS Chemical Neuroscience Pub Date : 2024-03-19 DOI:10.1021/acschemneuro.4c00003
Thin Thin San, Junhyung Kim and Hyun-Jung Kim*, 
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Abstract

Lysine-specific histone demethylase 5A (KDM5A) is known to facilitate proliferation in cancer cells and maintain stemness to repress the astrocytic differentiation of neural stem cells (NSCs). In the study presented here, we investigated the effect of a KDM5 inhibitor, CPI-455, on NSC fate control. CPI-455 induced astrocytogenesis in NSCs during differentiation. Kdm5a, but not Kdm5c, knockdown induced glial fibrillary acidic protein (Gfap) transcription. CPI-455 induced signal transducer and activator of transcription 3, increased bone morphogenetic protein 2 expression, and enhanced mothers against decapentaplegic homolog 1/5/9 phosphorylation. The treatment of CPI-455 enhanced the methylation of histone H3 lysine 4 in the Gfap promoter when compared to that of the dimethyl sulfoxide control. In addition, CPI-455 treatment significantly reduced the recruitment of KDM5A to the Gfap promoter. Our data suggest that the KDM5 inhibitor CPI-455 effectively controls NSC cell fate via KDM5A inhibition and induces astrocytogenesis.

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组蛋白赖氨酸去甲基化酶 KDM5 抑制剂 CPI-455 可诱导神经干细胞的星形胶质细胞生成
众所周知,赖氨酸特异性组蛋白去甲基化酶5A(KDM5A)可促进癌细胞增殖,并保持干性,抑制神经干细胞(NSC)的星形胶质细胞分化。在本研究中,我们研究了KDM5抑制剂CPI-455对NSC命运控制的影响。在分化过程中,CPI-455诱导了NSC的星形胶质细胞生成。Kdm5a(而非Kdm5c)敲除可诱导胶质纤维酸性蛋白(Gfap)转录。CPI-455诱导信号转导子和转录激活子3,增加骨形态发生蛋白2的表达,并增强母体抗截瘫同源物1/5/9的磷酸化。与二甲基亚砜对照组相比,CPI-455 能增强 Gfap 启动子中组蛋白 H3 赖氨酸 4 的甲基化。此外,CPI-455 处理还显著降低了 KDM5A 对 Gfap 启动子的招募。我们的数据表明,KDM5抑制剂CPI-455可通过抑制KDM5A有效控制NSC细胞的命运,并诱导星形胶质细胞的生成。
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来源期刊
ACS Chemical Neuroscience
ACS Chemical Neuroscience BIOCHEMISTRY & MOLECULAR BIOLOGY-CHEMISTRY, MEDICINAL
CiteScore
9.20
自引率
4.00%
发文量
323
审稿时长
1 months
期刊介绍: ACS Chemical Neuroscience publishes high-quality research articles and reviews that showcase chemical, quantitative biological, biophysical and bioengineering approaches to the understanding of the nervous system and to the development of new treatments for neurological disorders. Research in the journal focuses on aspects of chemical neurobiology and bio-neurochemistry such as the following: Neurotransmitters and receptors Neuropharmaceuticals and therapeutics Neural development—Plasticity, and degeneration Chemical, physical, and computational methods in neuroscience Neuronal diseases—basis, detection, and treatment Mechanism of aging, learning, memory and behavior Pain and sensory processing Neurotoxins Neuroscience-inspired bioengineering Development of methods in chemical neurobiology Neuroimaging agents and technologies Animal models for central nervous system diseases Behavioral research
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