Brainwide Projections of Mouse Dopaminergic Zona Incerta Neurons

IF 2.1 4区 医学 Q3 NEUROSCIENCES
Bianca S. Bono, Kenichiro Negishi, Yasmina Dumiaty, Monica S. Ponce-Ruiz, Titilayo C. Akinbode, Kayla S. Baker, C. Duncan P. Spencer, Elizabeth Mejia, Marina Guirguis, Alex J. Hebert, Arshad M. Khan, Melissa J. Chee
{"title":"Brainwide Projections of Mouse Dopaminergic Zona Incerta Neurons","authors":"Bianca S. Bono,&nbsp;Kenichiro Negishi,&nbsp;Yasmina Dumiaty,&nbsp;Monica S. Ponce-Ruiz,&nbsp;Titilayo C. Akinbode,&nbsp;Kayla S. Baker,&nbsp;C. Duncan P. Spencer,&nbsp;Elizabeth Mejia,&nbsp;Marina Guirguis,&nbsp;Alex J. Hebert,&nbsp;Arshad M. Khan,&nbsp;Melissa J. Chee","doi":"10.1002/cne.70039","DOIUrl":null,"url":null,"abstract":"<p>The zona incerta (ZI) supports diverse behaviors including binge feeding, sleep–wake cycles, nociception, and hunting. Diverse ZI functions can be attributed to its heterogeneous neurochemical characterization, cytoarchitecture, and efferent connections. The ZI is predominantly GABAergic, but we recently identified a subset of medial ZI GABA cells that are marked by the enzyme tyrosine hydroxylase (TH) and produce dopamine (DA). While the role of GABA within the ZI is well studied, less is known about the functions of ZI DA cells. To identify potential roles of ZI DA cells, we further phenotyped them and mapped their efferent fiber projections. We showed that wild-type TH-immunoreactive (-ir) ZI cells did not express somatostatin or calretinin immunoreactivity. We next validated a <i>Th-cre;L10-Egfp</i> mouse line and found that medial <i>Egfp</i> ZI cells were more likely to be TH-ir. We therefore delivered a Cre-dependent virus into the medial ZI of <i>Th-cre</i> or <i>Th-cre;L10-Egfp</i> mice and selected two injection cases for full brain mapping, namely, cases with the lowest and highest colocalization between TH-ir and virally transduced, DsRed-labeled cells, to identify common target sites. Overall, DsRed-labeled fibers were distributed brainwide and were most prominent within the motor-related midbrain (MBmot), notably the periaqueductal gray area and superior colliculus. We also observed numerous DsRed-labeled fibers within the polymodal association cortex-related thalamus (DORpm), like paraventricular thalamic nucleus and nucleus of reunions, that processes external and internal sensory input. Overall, ZI DA cells displayed a similar fiber profile to ZI GABA cells and may integrate sensory input to coordinate motor output at their target sites.</p>","PeriodicalId":15552,"journal":{"name":"Journal of Comparative Neurology","volume":"533 3","pages":""},"PeriodicalIF":2.1000,"publicationDate":"2025-03-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cne.70039","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Comparative Neurology","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cne.70039","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

The zona incerta (ZI) supports diverse behaviors including binge feeding, sleep–wake cycles, nociception, and hunting. Diverse ZI functions can be attributed to its heterogeneous neurochemical characterization, cytoarchitecture, and efferent connections. The ZI is predominantly GABAergic, but we recently identified a subset of medial ZI GABA cells that are marked by the enzyme tyrosine hydroxylase (TH) and produce dopamine (DA). While the role of GABA within the ZI is well studied, less is known about the functions of ZI DA cells. To identify potential roles of ZI DA cells, we further phenotyped them and mapped their efferent fiber projections. We showed that wild-type TH-immunoreactive (-ir) ZI cells did not express somatostatin or calretinin immunoreactivity. We next validated a Th-cre;L10-Egfp mouse line and found that medial Egfp ZI cells were more likely to be TH-ir. We therefore delivered a Cre-dependent virus into the medial ZI of Th-cre or Th-cre;L10-Egfp mice and selected two injection cases for full brain mapping, namely, cases with the lowest and highest colocalization between TH-ir and virally transduced, DsRed-labeled cells, to identify common target sites. Overall, DsRed-labeled fibers were distributed brainwide and were most prominent within the motor-related midbrain (MBmot), notably the periaqueductal gray area and superior colliculus. We also observed numerous DsRed-labeled fibers within the polymodal association cortex-related thalamus (DORpm), like paraventricular thalamic nucleus and nucleus of reunions, that processes external and internal sensory input. Overall, ZI DA cells displayed a similar fiber profile to ZI GABA cells and may integrate sensory input to coordinate motor output at their target sites.

Abstract Image

小鼠多巴胺能不动带神经元的全脑投射
无食带(ZI)支持多种行为,包括暴食、睡眠-觉醒周期、伤害感受和狩猎。不同的ZI功能可归因于其不同的神经化学特征、细胞结构和传出连接。ZI主要是GABA能细胞,但我们最近发现了一个内侧ZI GABA细胞亚群,该亚群被酪氨酸羟化酶(TH)标记并产生多巴胺(DA)。虽然GABA在ZI中的作用研究得很好,但对ZI DA细胞的功能知之甚少。为了确定ZI DA细胞的潜在作用,我们进一步对它们进行表型分析,并绘制了它们的输出纤维投射图。我们发现野生型th免疫反应性(-ir) ZI细胞不表达生长抑素或calretinin免疫反应性。接下来,我们验证了Th-cre;L10-Egfp小鼠系,发现内侧Egfp ZI细胞更有可能是TH-ir。因此,我们将一种依赖于TH-ir的病毒注入Th-cre或Th-cre;L10-Egfp小鼠的内侧ZI中,并选择两例注射病例进行全脑定位,即TH-ir和病毒转导的dsred标记细胞之间共定位最低和最高的病例,以确定共同的靶点。总的来说,dsred标记的纤维分布在全脑范围内,在运动相关的中脑(MBmot)中最为突出,特别是导水管周围灰色区和上丘。我们还观察到,在处理外部和内部感觉输入的多模态关联皮层相关丘脑(DORpm)内,如室旁丘脑核和相聚核,有许多dsred标记的纤维。总的来说,ZI DA细胞显示出与ZI GABA细胞相似的纤维轮廓,并且可能整合感觉输入以协调目标部位的运动输出。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
5.80
自引率
8.00%
发文量
158
审稿时长
3-6 weeks
期刊介绍: Established in 1891, JCN is the oldest continually published basic neuroscience journal. Historically, as the name suggests, the journal focused on a comparison among species to uncover the intricacies of how the brain functions. In modern times, this research is called systems neuroscience where animal models are used to mimic core cognitive processes with the ultimate goal of understanding neural circuits and connections that give rise to behavioral patterns and different neural states. Research published in JCN covers all species from invertebrates to humans, and the reports inform the readers about the function and organization of nervous systems in species with an emphasis on the way that species adaptations inform about the function or organization of the nervous systems, rather than on their evolution per se. JCN publishes primary research articles and critical commentaries and review-type articles offering expert insight in to cutting edge research in the field of systems neuroscience; a complete list of contribution types is given in the Author Guidelines. For primary research contributions, only full-length investigative reports are desired; the journal does not accept short communications.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信