Retroviral lineage analysis reveals dual contribution from ectodermal placodes and neural crest cells to avian olfactory sensory and GnRH neurons.

IF 2.6 Q2 MULTIDISCIPLINARY SCIENCES Natural sciences (Weinheim, Germany) Pub Date : 2022-07-01 DOI:10.1002/ntls.20210037
Alison Koontz, Hugo A Urrutia, Marianne E Bronner
{"title":"Retroviral lineage analysis reveals dual contribution from ectodermal placodes and neural crest cells to avian olfactory sensory and GnRH neurons.","authors":"Alison Koontz,&nbsp;Hugo A Urrutia,&nbsp;Marianne E Bronner","doi":"10.1002/ntls.20210037","DOIUrl":null,"url":null,"abstract":"<p><p>The origin of the neurons and glia in the olfactory system of vertebrates has been controversial, with different cell types attributed to being of ectodermal placode versus neural crest lineage, depending upon the species. Here, we use replication incompetent avian (RIA) retroviruses to perform prospective cell lineage analysis of either presumptive olfactory placode or neural crest cells during early development of the chick embryo. Surprisingly, the results reveal a dual contribution from both the olfactory placode and neural crest cells to sensory neurons in the nose and Gonadotropin Releasing Hormone (GnRH) neurons migrating to the olfactory bulb. We also confirm that olfactory ensheathing glia are solely derived from the neural crest. Finally, our results show that neural crest cells and olfactory placode cells contribute to p63 positive cells, likely to be basal stem cells of the olfactory epithelium. Taken together, these finding provide evidence for previously unknown contributions of neural crest cells to some cell types in the chick olfactory system and help resolve previous discrepancies in the literature.</p>","PeriodicalId":74244,"journal":{"name":"Natural sciences (Weinheim, Germany)","volume":null,"pages":null},"PeriodicalIF":2.6000,"publicationDate":"2022-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9605686/pdf/nihms-1807638.pdf","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Natural sciences (Weinheim, Germany)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/ntls.20210037","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
引用次数: 1

Abstract

The origin of the neurons and glia in the olfactory system of vertebrates has been controversial, with different cell types attributed to being of ectodermal placode versus neural crest lineage, depending upon the species. Here, we use replication incompetent avian (RIA) retroviruses to perform prospective cell lineage analysis of either presumptive olfactory placode or neural crest cells during early development of the chick embryo. Surprisingly, the results reveal a dual contribution from both the olfactory placode and neural crest cells to sensory neurons in the nose and Gonadotropin Releasing Hormone (GnRH) neurons migrating to the olfactory bulb. We also confirm that olfactory ensheathing glia are solely derived from the neural crest. Finally, our results show that neural crest cells and olfactory placode cells contribute to p63 positive cells, likely to be basal stem cells of the olfactory epithelium. Taken together, these finding provide evidence for previously unknown contributions of neural crest cells to some cell types in the chick olfactory system and help resolve previous discrepancies in the literature.

Abstract Image

Abstract Image

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
逆转录病毒谱系分析揭示了外胚层基板细胞和神经嵴细胞对鸟类嗅觉感觉和GnRH神经元的双重贡献。
脊椎动物嗅觉系统中神经元和神经胶质的起源一直存在争议,根据物种的不同,有不同的细胞类型被归因于外胚层基板和神经嵴谱系。在这里,我们使用复制不能力禽(RIA)逆转录病毒对鸡胚胎早期发育过程中推测的嗅觉基板细胞或神经嵴细胞进行前瞻性细胞谱系分析。令人惊讶的是,结果显示嗅觉基板和神经嵴细胞对鼻子的感觉神经元和促性腺激素释放激素(GnRH)神经元迁移到嗅球的双重贡献。我们也证实了嗅鞘胶质细胞完全来源于神经嵴。最后,我们的研究结果表明,神经嵴细胞和嗅觉基板细胞有助于p63阳性细胞,可能是嗅觉上皮的基底干细胞。综上所述,这些发现为以前未知的神经嵴细胞对鸡嗅觉系统中某些细胞类型的贡献提供了证据,并有助于解决先前文献中的差异。
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 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Comparative proteomic analysis of tail regeneration in the green anole lizard, Anolis carolinensis. Isotope effect suggests site‐specific nonadiabaticity on Ge(111)c(2×8) Automated segmentation of insect anatomy from micro‐CT images using deep learning The propagation of Hermite–Gauss wave packets in optics and quantum mechanics Exhaled aerosols and saliva droplets measured in time and 3D space: Quantification of pathogens flow rate applied to SARS‐CoV‐2
×
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