Suppr超能文献

氧化应激调节祖细胞行为和皮质神经发生。

Oxidative stress regulates progenitor behavior and cortical neurogenesis.

机构信息

Developmental Biology Program, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, 1275 York Avenue, New York, NY 10065, USA

Neuroscience Graduate Program, Weill Cornell Medical College, 1300 York Avenue, New York, NY 10065, USA.

出版信息

Development. 2020 Mar 11;147(5):dev184150. doi: 10.1242/dev.184150.

Abstract

Orderly division of radial glial progenitors (RGPs) in the developing mammalian cerebral cortex generates deep and superficial layer neurons progressively. However, the mechanisms that control RGP behavior and precise neuronal output remain elusive. Here, we show that the oxidative stress level progressively increases in the developing mouse cortex and regulates RGP behavior and neurogenesis. As development proceeds, numerous gene pathways linked to reactive oxygen species (ROS) and oxidative stress exhibit drastic changes in RGPs. Selective removal of PRDM16, a transcriptional regulator highly expressed in RGPs, elevates ROS level and induces expression of oxidative stress-responsive genes. Coinciding with an enhanced level of oxidative stress, RGP behavior was altered, leading to abnormal deep and superficial layer neuron generation. Simultaneous expression of mitochondrially targeted catalase to reduce cellular ROS levels significantly suppresses cortical defects caused by PRDM16 removal. Together, these findings suggest that oxidative stress actively regulates RGP behavior to ensure proper neurogenesis in the mammalian cortex.

摘要

在哺乳动物大脑皮层的发育过程中,放射状胶质前体细胞(RGPs)有序分裂,逐渐产生深层和浅层神经元。然而,控制 RGPs 行为和精确神经元输出的机制仍不清楚。在这里,我们发现发育中的小鼠皮层中的氧化应激水平逐渐升高,并调节 RGPs 的行为和神经发生。随着发育的进行,与活性氧(ROS)和氧化应激相关的许多基因途径在 RGPs 中发生剧烈变化。选择性去除 PRDM16,一种在 RGPs 中高度表达的转录调节剂,会升高 ROS 水平并诱导氧化应激反应基因的表达。与氧化应激水平的升高相吻合,RGPs 的行为发生改变,导致深层和浅层神经元生成异常。同时表达靶向线粒体的过氧化氢酶以降低细胞内 ROS 水平,可显著抑制 PRDM16 缺失引起的皮质缺陷。总之,这些发现表明氧化应激积极调节 RGPs 的行为,以确保哺乳动物皮层中适当的神经发生。

相似文献

1
Oxidative stress regulates progenitor behavior and cortical neurogenesis.
Development. 2020 Mar 11;147(5):dev184150. doi: 10.1242/dev.184150.
4
Cortical neurogenesis in the absence of centrioles.
Nat Neurosci. 2014 Nov;17(11):1528-35. doi: 10.1038/nn.3831. Epub 2014 Oct 5.
5
CHD2 is Required for Embryonic Neurogenesis in the Developing Cerebral Cortex.
Stem Cells. 2015 Jun;33(6):1794-806. doi: 10.1002/stem.2001.
6
The Epigenetic State of PRDM16-Regulated Enhancers in Radial Glia Controls Cortical Neuron Position.
Neuron. 2018 Jun 6;98(5):945-962.e8. doi: 10.1016/j.neuron.2018.04.033. Epub 2018 May 17.
7
Deterministic progenitor behavior and unitary production of neurons in the neocortex.
Cell. 2014 Nov 6;159(4):775-88. doi: 10.1016/j.cell.2014.10.027.
9
Mosaic Analysis with Double Markers Reveals Distinct Sequential Functions of Lgl1 in Neural Stem Cells.
Neuron. 2017 May 3;94(3):517-533.e3. doi: 10.1016/j.neuron.2017.04.012.
10
Adult neurogenesis transiently generates oxidative stress.
PLoS One. 2012;7(4):e35264. doi: 10.1371/journal.pone.0035264. Epub 2012 Apr 30.

引用本文的文献

1
Prdm16 regulates the postnatal fate of embryonic radial glia via Vcam1-dependent mechanisms.
Nat Commun. 2025 Jul 19;16(1):6659. doi: 10.1038/s41467-025-60895-y.
3
Effects of gestational hypothyroidism on mouse brain development: Gabaergic systems and oxidative stress.
Dev Biol. 2024 Nov;515:112-120. doi: 10.1016/j.ydbio.2024.07.010. Epub 2024 Jul 22.
4
PRDM16 co-operates with LHX2 to shape the human brain.
Oxf Open Neurosci. 2024 Jan 24;3:kvae001. doi: 10.1093/oons/kvae001. eCollection 2024.
6
Toward reframing brain-social dynamics: current assumptions and future challenges.
Front Psychiatry. 2023 Jul 6;14:1211442. doi: 10.3389/fpsyt.2023.1211442. eCollection 2023.
7
Neurodevelopmental disorders: 2023 update.
Free Neuropathol. 2023 May 8;4:8. doi: 10.17879/freeneuropathology-2023-4701. eCollection 2023 Jan.
8
Temporal transcriptional control of neural induction in human induced pluripotent stem cells.
Front Mol Neurosci. 2023 May 5;16:1139287. doi: 10.3389/fnmol.2023.1139287. eCollection 2023.
9
Epigenetic Alterations under Oxidative Stress in Stem Cells.
Oxid Med Cell Longev. 2022 Aug 29;2022:6439097. doi: 10.1155/2022/6439097. eCollection 2022.
10
De novo variants in genes regulating stress granule assembly associate with neurodevelopmental disorders.
Sci Adv. 2022 Aug 19;8(33):eabo7112. doi: 10.1126/sciadv.abo7112. Epub 2022 Aug 17.

本文引用的文献

2
Pharmacological Regulation of Oxidative Stress in Stem Cells.
Oxid Med Cell Longev. 2018 Sep 30;2018:4081890. doi: 10.1155/2018/4081890. eCollection 2018.
4
The Epigenetic State of PRDM16-Regulated Enhancers in Radial Glia Controls Cortical Neuron Position.
Neuron. 2018 Jun 6;98(5):945-962.e8. doi: 10.1016/j.neuron.2018.04.033. Epub 2018 May 17.
5
Exogenous pentraxin-3 inhibits the reactive oxygen species-mitochondrial and apoptosis pathway in acute kidney injury.
PLoS One. 2018 Apr 19;13(4):e0195758. doi: 10.1371/journal.pone.0195758. eCollection 2018.
6
Superoxide dismutases: Dual roles in controlling ROS damage and regulating ROS signaling.
J Cell Biol. 2018 Jun 4;217(6):1915-1928. doi: 10.1083/jcb.201708007. Epub 2018 Apr 18.
7
Retinoic acid controls early neurogenesis in the developing mouse cerebral cortex.
Dev Biol. 2017 Oct 1;430(1):129-141. doi: 10.1016/j.ydbio.2017.08.006. Epub 2017 Aug 5.
9
Mitochondrial-Targeted Catalase: Extended Longevity and the Roles in Various Disease Models.
Prog Mol Biol Transl Sci. 2017;146:203-241. doi: 10.1016/bs.pmbts.2016.12.015. Epub 2017 Feb 4.
10
Prdm16 is crucial for progression of the multipolar phase during neural differentiation of the developing neocortex.
Development. 2017 Feb 1;144(3):385-399. doi: 10.1242/dev.136382. Epub 2016 Dec 19.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验