Temporal and clonal characterization of neural stem cell niche recruitment in the medaka neuromast

IF 3.9 4区 生物学 Q4 Biochemistry, Genetics and Molecular Biology
Jasmin Onistschenko, Sabrina Kaminsky, Javier Vazquez-Marín, Karen Gross, Tianyu Wang , Ali Seleit , Melanie Dörr , Lázaro Centanin
{"title":"Temporal and clonal characterization of neural stem cell niche recruitment in the medaka neuromast","authors":"Jasmin Onistschenko,&nbsp;Sabrina Kaminsky,&nbsp;Javier Vazquez-Marín,&nbsp;Karen Gross,&nbsp;Tianyu Wang ,&nbsp;Ali Seleit ,&nbsp;Melanie Dörr ,&nbsp;Lázaro Centanin","doi":"10.1016/j.cdev.2023.203837","DOIUrl":null,"url":null,"abstract":"<div><p>Stem cell populations are defined by their capacity to self-renew and to generate differentiated progeny. These unique characteristics largely depend on the stem cell micro-environment, the so-called stem cell niche. Niches were identified for most adult stem cells studied so far, but we know surprisingly little about how somatic stem cells and their niche come together during organ formation. Using the neuromasts of teleost fish, we have previously reported that neural stem cells recruit their niche from neighboring epithelial cells, which go through a morphological and molecular transformation. Here, we tackle quantitative, temporal, and clonal aspects of niche formation in neuromasts by using 4D imaging in transgenic lines, and lineage analysis in mosaic fish. We show that niche recruitment happens in a defined temporal window during the formation of neuromasts in medaka, and after that, the niche is enlarged mainly by the proliferation of niche cells. Niche recruitment is a non-clonal process that feeds from diverse epithelial cells that do not display a preferential position along the circumference of the forming neuromast. Additionally, we cover niche formation and expansion in zebrafish to show that distant species show common features during organogenesis in the lateral line system. Overall, our findings shed light on the process of niche formation, fundamental for the maintenance of stem cells not only in medaka but also in many other multicellular organisms.</p></div>","PeriodicalId":36123,"journal":{"name":"Cells and Development","volume":"174 ","pages":"Article 203837"},"PeriodicalIF":3.9000,"publicationDate":"2023-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cells and Development","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S266729012300013X","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 0

Abstract

Stem cell populations are defined by their capacity to self-renew and to generate differentiated progeny. These unique characteristics largely depend on the stem cell micro-environment, the so-called stem cell niche. Niches were identified for most adult stem cells studied so far, but we know surprisingly little about how somatic stem cells and their niche come together during organ formation. Using the neuromasts of teleost fish, we have previously reported that neural stem cells recruit their niche from neighboring epithelial cells, which go through a morphological and molecular transformation. Here, we tackle quantitative, temporal, and clonal aspects of niche formation in neuromasts by using 4D imaging in transgenic lines, and lineage analysis in mosaic fish. We show that niche recruitment happens in a defined temporal window during the formation of neuromasts in medaka, and after that, the niche is enlarged mainly by the proliferation of niche cells. Niche recruitment is a non-clonal process that feeds from diverse epithelial cells that do not display a preferential position along the circumference of the forming neuromast. Additionally, we cover niche formation and expansion in zebrafish to show that distant species show common features during organogenesis in the lateral line system. Overall, our findings shed light on the process of niche formation, fundamental for the maintenance of stem cells not only in medaka but also in many other multicellular organisms.

medaka神经肥大神经干细胞生态位募集的时间和克隆特征
干细胞群体的定义是其自我更新和产生分化后代的能力。这些独特的特征在很大程度上取决于干细胞的微环境,即所谓的干细胞生态位。到目前为止,大多数研究的成年干细胞都有小生境,但令人惊讶的是,我们对体细胞干细胞及其小生境在器官形成过程中是如何结合在一起的知之甚少。使用硬骨鱼的神经模型,我们之前已经报道了神经干细胞从相邻的上皮细胞中募集其生态位,这些上皮细胞经过形态学和分子转化。在这里,我们通过在转基因系中使用4D成像和在镶嵌鱼中使用谱系分析来解决神经瘤中生态位形成的数量、时间和克隆方面的问题。我们发现,在小生境形成过程中,小生境的募集发生在一个确定的时间窗口内,在此之后,小生境主要通过小生境细胞的增殖而扩大。小生境募集是一种非克隆过程,其来源于不同的上皮细胞,这些上皮细胞在形成神经基质的圆周上没有显示出优先位置。此外,我们还报道了斑马鱼的生态位形成和扩展,以表明远缘物种在侧线系统的器官发生过程中表现出共同的特征。总的来说,我们的发现揭示了生态位形成的过程,这不仅是维护梅达卡干细胞的基础,也是维护许多其他多细胞生物的基础。
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
Cells and Development
Cells and Development Biochemistry, Genetics and Molecular Biology-Developmental Biology
CiteScore
2.90
自引率
0.00%
发文量
33
审稿时长
41 days
×
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:481959085
Book学术官方微信