显性阴性DISC1改变小鼠前额叶皮层抑制性中间神经元的多巴胺能调节。

Molecular Neuropsychiatry Pub Date : 2018-06-01 Epub Date: 2018-05-07 DOI:10.1159/000488030
Ross A Cardarelli, Rolicia Martin, Hanna Jaaro-Peled, Akira Sawa, Elizabeth M Powell, Patricio O'Donnell
{"title":"显性阴性DISC1改变小鼠前额叶皮层抑制性中间神经元的多巴胺能调节。","authors":"Ross A Cardarelli,&nbsp;Rolicia Martin,&nbsp;Hanna Jaaro-Peled,&nbsp;Akira Sawa,&nbsp;Elizabeth M Powell,&nbsp;Patricio O'Donnell","doi":"10.1159/000488030","DOIUrl":null,"url":null,"abstract":"<p><p>A truncated <i>disrupted in schizophrenia 1</i> (<i>Disc1</i>) gene increases the risk of psychiatric disorders, probably affecting cortical interneurons. Here, we sought to determine whether this cell population is affected in mice carrying a truncated (<i>Disc1</i>) allele (DN-DISC1). We utilized whole cell recordings to assess electrophysiological properties and modulation by dopamine (DA) in two classes of interneurons: fast-spiking (FS) and low threshold-spiking (LTS) interneurons in wild-type and DN-DISC1 mice. In DN-DISC1 mice, FS interneurons, but not LTS interneurons, exhibited altered action potentials. Further, the perineuronal nets that surround FS interneurons exhibited abnormal morphology in DN-DISC1 mice, and the DA modulation of this cell type was altered in DN-DISC1 mice. We conclude that early-life manipulation of a gene associated with risk of psychiatric disease can result in dysfunction, but not loss, of specific GABAergic interneurons. The resulting alteration of excitatory-inhibitory balance is a critical element in DISC1 pathophysiology.</p>","PeriodicalId":18957,"journal":{"name":"Molecular Neuropsychiatry","volume":"4 1","pages":"20-29"},"PeriodicalIF":0.0000,"publicationDate":"2018-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000488030","citationCount":"6","resultStr":"{\"title\":\"Dominant-Negative DISC1 Alters the Dopaminergic Modulation of Inhibitory Interneurons in the Mouse Prefrontal Cortex.\",\"authors\":\"Ross A Cardarelli,&nbsp;Rolicia Martin,&nbsp;Hanna Jaaro-Peled,&nbsp;Akira Sawa,&nbsp;Elizabeth M Powell,&nbsp;Patricio O'Donnell\",\"doi\":\"10.1159/000488030\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>A truncated <i>disrupted in schizophrenia 1</i> (<i>Disc1</i>) gene increases the risk of psychiatric disorders, probably affecting cortical interneurons. Here, we sought to determine whether this cell population is affected in mice carrying a truncated (<i>Disc1</i>) allele (DN-DISC1). We utilized whole cell recordings to assess electrophysiological properties and modulation by dopamine (DA) in two classes of interneurons: fast-spiking (FS) and low threshold-spiking (LTS) interneurons in wild-type and DN-DISC1 mice. In DN-DISC1 mice, FS interneurons, but not LTS interneurons, exhibited altered action potentials. Further, the perineuronal nets that surround FS interneurons exhibited abnormal morphology in DN-DISC1 mice, and the DA modulation of this cell type was altered in DN-DISC1 mice. We conclude that early-life manipulation of a gene associated with risk of psychiatric disease can result in dysfunction, but not loss, of specific GABAergic interneurons. The resulting alteration of excitatory-inhibitory balance is a critical element in DISC1 pathophysiology.</p>\",\"PeriodicalId\":18957,\"journal\":{\"name\":\"Molecular Neuropsychiatry\",\"volume\":\"4 1\",\"pages\":\"20-29\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2018-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1159/000488030\",\"citationCount\":\"6\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Molecular Neuropsychiatry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1159/000488030\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2018/5/7 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Neuropsychiatry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1159/000488030","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2018/5/7 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 6

摘要

精神分裂症1 (Disc1)基因的截断破坏增加了精神疾病的风险,可能影响皮质中间神经元。在这里,我们试图确定携带截断(Disc1)等位基因(DN-DISC1)的小鼠是否会影响该细胞群。我们利用全细胞记录来评估野生型和DN-DISC1小鼠两类中间神经元的电生理特性和多巴胺(DA)的调节:快速峰值(FS)和低阈值峰值(LTS)中间神经元。在DN-DISC1小鼠中,FS中间神经元而非LTS中间神经元表现出改变的动作电位。此外,在DN-DISC1小鼠中,围绕FS中间神经元的神经元周围网表现出异常形态,并且该细胞类型的DA调节在DN-DISC1小鼠中发生了改变。我们的结论是,生命早期对与精神疾病风险相关的基因的操作可能导致特定gaba能中间神经元的功能障碍,但不会丢失。由此引起的兴奋-抑制平衡的改变是DISC1病理生理的一个关键因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

摘要图片

摘要图片

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Dominant-Negative DISC1 Alters the Dopaminergic Modulation of Inhibitory Interneurons in the Mouse Prefrontal Cortex.

A truncated disrupted in schizophrenia 1 (Disc1) gene increases the risk of psychiatric disorders, probably affecting cortical interneurons. Here, we sought to determine whether this cell population is affected in mice carrying a truncated (Disc1) allele (DN-DISC1). We utilized whole cell recordings to assess electrophysiological properties and modulation by dopamine (DA) in two classes of interneurons: fast-spiking (FS) and low threshold-spiking (LTS) interneurons in wild-type and DN-DISC1 mice. In DN-DISC1 mice, FS interneurons, but not LTS interneurons, exhibited altered action potentials. Further, the perineuronal nets that surround FS interneurons exhibited abnormal morphology in DN-DISC1 mice, and the DA modulation of this cell type was altered in DN-DISC1 mice. We conclude that early-life manipulation of a gene associated with risk of psychiatric disease can result in dysfunction, but not loss, of specific GABAergic interneurons. The resulting alteration of excitatory-inhibitory balance is a critical element in DISC1 pathophysiology.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Genome-Wide Association Study of Sleep Disturbances in Depressive Disorders. EAAT2 as a Research Target in Bipolar Disorder and Unipolar Depression: A Systematic Review. The Role of PTEN in Neurodevelopment. Using Chronobiological Phenotypes to Address Heterogeneity in Bipolar Disorder. The Genetic Relevance of Human Induced Pluripotent Stem Cell-Derived Microglia to Alzheimer's Disease and Major Neuropsychiatric Disorders.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1