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本文引用的文献

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Molecular diversity of early-born subplate neurons.早期出生的基板下神经元的分子多样性。
Cereb Cortex. 2013 Jun;23(6):1473-83. doi: 10.1093/cercor/bhs137. Epub 2012 May 23.
2
Mosaic: making biological sense of complex networks.马赛克:从复杂网络中理解生物学意义
Bioinformatics. 2012 Jul 15;28(14):1943-4. doi: 10.1093/bioinformatics/bts278. Epub 2012 May 9.
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The emerging spectrum of allelic variation in schizophrenia: current evidence and strategies for the identification and functional characterization of common and rare variants.精神分裂症中不断出现的等位基因变异谱:常见和罕见变异的鉴定和功能特征的当前证据和策略。
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4
Evidence that descending cortical axons are essential for thalamocortical axons to cross the pallial-subpallial boundary in the embryonic forebrain.证明皮质下轴突对于胚胎前脑的丘脑皮质轴突穿过皮层下边界是必不可少的。
PLoS One. 2012;7(3):e33105. doi: 10.1371/journal.pone.0033105. Epub 2012 Mar 8.
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A transcriptomic atlas of mouse neocortical layers.鼠大脑新皮层层的转录组图谱。
Neuron. 2011 Aug 25;71(4):605-16. doi: 10.1016/j.neuron.2011.06.039.
6
Gene expression analysis of the embryonic subplate.胚胎基板的基因表达分析。
Cereb Cortex. 2012 Jun;22(6):1343-59. doi: 10.1093/cercor/bhr197. Epub 2011 Aug 22.
7
Neurexin-1 and frontal lobe white matter: an overlapping intermediate phenotype for schizophrenia and autism spectrum disorders.神经连接蛋白-1 和额叶白质:精神分裂症和自闭症谱系障碍的重叠中间表型。
PLoS One. 2011;6(6):e20982. doi: 10.1371/journal.pone.0020982. Epub 2011 Jun 8.
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Differential distribution of neurons in the gyral white matter of the human cerebral cortex.人类大脑皮层脑回白质中神经元的差异分布。
J Comp Neurol. 2010 Dec 1;518(23):4740-59. doi: 10.1002/cne.22485.
9
Developmental history of the subplate zone, subplate neurons and interstitial white matter neurons: relevance for schizophrenia.板下层区域、板下神经元和间质白质神经元的发育史:与精神分裂症的相关性
Int J Dev Neurosci. 2011 May;29(3):193-205. doi: 10.1016/j.ijdevneu.2010.09.005. Epub 2010 Sep 29.
10
Abnormal cell patterning at the cortical gray-white matter boundary in autism spectrum disorders.自闭症谱系障碍患者皮质灰白质边界处的细胞排列异常。
Brain Res. 2010 Nov 11;1360:138-46. doi: 10.1016/j.brainres.2010.08.091. Epub 2010 Sep 25.

小鼠基板表达谱分析揭示了一个动态的基因网络,并与自闭症和精神分裂症存在疾病关联。

Expression profiling of mouse subplate reveals a dynamic gene network and disease association with autism and schizophrenia.

机构信息

Department of Physiology, Anatomy and Genetics, University of Oxford, Oxford OX1 3QX, United Kingdom.

出版信息

Proc Natl Acad Sci U S A. 2013 Feb 26;110(9):3555-60. doi: 10.1073/pnas.1218510110. Epub 2013 Feb 11.

DOI:10.1073/pnas.1218510110
PMID:23401504
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3587197/
Abstract

The subplate zone is a highly dynamic transient sector of the developing cerebral cortex that contains some of the earliest generated neurons and the first functional synapses of the cerebral cortex. Subplate cells have important functions in early establishment and maturation of thalamocortical connections, as well as in the development of inhibitory cortical circuits in sensory areas. So far no role has been identified for cells in the subplate in the mature brain and disease association of the subplate-specific genes has not been analyzed systematically. Here we present gene expression evidence for distinct roles of the mouse subplate across development as well as unique molecular markers to extend the repertoire of subplate labels. Performing systematic comparisons between different ages (embryonic days 15 and 18, postnatal day 8, and adult), we reveal the dynamic and constant features of the markers labeling subplate cells during embryonic and early postnatal development and in the adult. This can be visualized using the online database of subplate gene expression at https://molnar.dpag.ox.ac.uk/subplate/. We also identify embryonic similarities in gene expression between the ventricular zones, intermediate zone, and subplate, and distinct postnatal similarities between subplate, layer 5, and layers 2/3. The genes expressed in a subplate-specific manner at some point during development show a statistically significant enrichment for association with autism spectrum disorders and schizophrenia. Our report emphasizes the importance of the study of transient features of the developing brain to better understand neurodevelopmental disorders.

摘要

基板层是发育中的大脑皮层中一个高度动态的暂存区,包含一些最早产生的神经元和大脑皮层的第一个功能性突触。基板细胞在早期建立和成熟丘脑皮质连接以及在感觉区域抑制性皮质回路的发育中具有重要功能。到目前为止,尚未确定成熟大脑中基板细胞的作用,也没有系统地分析基板特异性基因与疾病的关联。在这里,我们提出了关于小鼠基板在整个发育过程中的不同作用的基因表达证据,以及独特的分子标记来扩展基板标记的范围。通过在不同年龄(胚胎第 15 天和第 18 天、出生后第 8 天和成年)之间进行系统比较,我们揭示了在胚胎和早期出生后发育以及成年期间标记基板细胞的标记物的动态和恒定特征。这可以使用 https://molnar.dpag.ox.ac.uk/subplate/ 上的基板基因表达在线数据库进行可视化。我们还发现,在胚胎期,脑室区、中间区和基板之间的基因表达存在相似性,而在出生后,基板、第 5 层和第 2/3 层之间的基因表达存在相似性。在发育过程中的某个时间点以基板特异性方式表达的基因与自闭症谱系障碍和精神分裂症有统计学意义的关联。我们的报告强调了研究发育中大脑的瞬态特征对于更好地理解神经发育障碍的重要性。