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使用脑回哺乳动物雪貂对大脑皮质折叠的发育和疾病进行分子研究。

Molecular Investigations of the Development and Diseases of Cerebral Cortex Folding using Gyrencephalic Mammal Ferrets.

作者信息

Kawasaki Hiroshi

机构信息

Department of Medical Neuroscience, Graduate School of Medical Sciences, Kanazawa University.

出版信息

Biol Pharm Bull. 2018;41(9):1324-1329. doi: 10.1248/bpb.b18-00142.

DOI:10.1248/bpb.b18-00142
PMID:30175769
Abstract

Folds of the cerebral cortex (gyri and sulci) are among the most important properties of the mammalian brain. Uncovering the physiological roles, developmental mechanisms and evolution of the cortical folds would greatly facilitate our understanding of the human brain and its diseases. Although the anatomical features of the cortical folds have been intensively investigated, our knowledge about their molecular bases is still limited. To overcome this limitation, we recently established rapid and efficient genetic manipulation techniques for the brain of gyrencephalic mammal ferrets (Mustela putorius furo). Using these techniques, we successfully uncovered the molecular mechanisms of cortical folding. In this article, I will summarize our recent research on the molecular mechanisms of development and diseases of cortical folding.

摘要

大脑皮层褶皱(脑回和脑沟)是哺乳动物大脑最重要的特征之一。揭示皮层褶皱的生理作用、发育机制和进化过程将极大地促进我们对人类大脑及其疾病的理解。尽管对皮层褶皱的解剖特征已进行了深入研究,但我们对其分子基础的了解仍然有限。为了克服这一局限,我们最近建立了针对脑回哺乳动物雪貂(白鼬)大脑的快速有效的基因操作技术。利用这些技术,我们成功揭示了皮层折叠的分子机制。在本文中,我将总结我们最近关于皮层折叠发育和疾病分子机制的研究。

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Molecular Investigations of the Development and Diseases of Cerebral Cortex Folding using Gyrencephalic Mammal Ferrets.使用脑回哺乳动物雪貂对大脑皮质折叠的发育和疾病进行分子研究。
Biol Pharm Bull. 2018;41(9):1324-1329. doi: 10.1248/bpb.b18-00142.
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Molecular investigations of the brain of higher mammals using gyrencephalic carnivore ferrets.使用脑回状食肉动物雪貂对高等哺乳动物大脑进行分子研究。
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Molecular investigations of development and diseases of the brain of higher mammals using the ferret.利用雪貂对高等哺乳动物大脑的发育和疾病进行分子研究。
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[Investigation of the Mechanisms Underlying Development and Diseases of the Cerebral Cortex Using Mice and Ferrets].利用小鼠和雪貂对大脑皮层发育及疾病潜在机制的研究
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An essential role of SVZ progenitors in cortical folding in gyrencephalic mammals.SVZ 祖细胞在卷褶脑哺乳动物皮质折叠中的重要作用。
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Folding of the Cerebral Cortex Requires Cdk5 in Upper-Layer Neurons in Gyrencephalic Mammals.大脑皮质折叠需要回旋脑哺乳动物上层神经元中的Cdk5。
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Investigation of the Mechanisms Underlying the Development and Evolution of the Cerebral Cortex Using Gyrencephalic Ferrets.使用脑回状雪貂研究大脑皮质发育和进化的潜在机制
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Gyrification of the cerebral cortex requires FGF signaling in the mammalian brain.大脑皮层的回旋需要哺乳动物大脑中的 FGF 信号。
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Pathophysiological analyses of cortical malformation using gyrencephalic mammals.使用脑回哺乳动物对皮质畸形进行病理生理学分析。
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Investigation of the mechanisms underlying the development and evolution of folds of the cerebrum using gyrencephalic ferrets.利用脑回卷曲的雪貂研究大脑褶皱发育和进化的潜在机制。
J Comp Neurol. 2024 Apr;532(4):e25615. doi: 10.1002/cne.25615.

引用本文的文献

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Longitudinal MRI of the developing ferret brain reveals regional variations in timing and rate of growth.纵向 MRI 研究揭示了雪貂大脑发育过程中的区域性生长时间和速度变化。
Cereb Cortex. 2024 Apr 1;34(4). doi: 10.1093/cercor/bhae172.
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Phosphorylation of GAP-43 T172 is a molecular marker of growing axons in a wide range of mammals including primates.磷酸化 GAP-43 T172 是包括灵长类动物在内的多种哺乳动物中生长轴突的分子标志物。
Mol Brain. 2021 Apr 8;14(1):66. doi: 10.1186/s13041-021-00755-0.
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Anomalous brain gyrification patterns in major psychiatric disorders: a systematic review and transdiagnostic integration.
主要精神疾病中的异常脑回模式:系统综述和跨诊断整合。
Transl Psychiatry. 2021 Mar 17;11(1):176. doi: 10.1038/s41398-021-01297-8.
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Role of in the Development and Evolution of the Gyrified Cortex.[此处英文单词不完整,请补充完整后再让我翻译]在脑回化皮质发育和演化中的作用。
Front Neurosci. 2020 Dec 18;14:617513. doi: 10.3389/fnins.2020.617513. eCollection 2020.
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Extracellular matrix-inducing Sox9 promotes both basal progenitor proliferation and gliogenesis in developing neocortex.细胞外基质诱导 Sox9 促进发育新皮层中的基底祖细胞增殖和神经胶质发生。
Elife. 2020 Mar 19;9:e49808. doi: 10.7554/eLife.49808.
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Malformations of Human Neocortex in Development - Their Progenitor Cell Basis and Experimental Model Systems.发育中的人类新皮质畸形——其祖细胞基础及实验模型系统
Front Cell Neurosci. 2019 Jul 9;13:305. doi: 10.3389/fncel.2019.00305. eCollection 2019.