秀丽隐杆线虫感觉器官的胚胎发育

IF 2.1 4区 医学 Q3 NEUROSCIENCES
Leland R. Wexler, Irina Kolotuev, Maxwell G. Heiman
{"title":"秀丽隐杆线虫感觉器官的胚胎发育","authors":"Leland R. Wexler,&nbsp;Irina Kolotuev,&nbsp;Maxwell G. Heiman","doi":"10.1002/cne.70084","DOIUrl":null,"url":null,"abstract":"<p><i>Caenorhabditis elegans</i> sense organs provide a powerful model for understanding how different cell types interact to assemble a functional organ. Each sense organ is composed of two glial cells, called the sheath and socket, and one or more neurons. A major challenge in studying their development has been the lack of methods to directly observe these structures in the embryo. Here, we mine a recently published high-resolution ultrastructural dataset of a comma-stage embryo that provides an untapped resource for visualizing early developmental events. From this dataset, we reconstructed all head sense organs (two amphid [AM], four cephalic [CEP], six inner labial [IL], four outer labial quadrant [OLQ], and two outer labial lateral [OLL]). Symmetric sense organs were at different stages of morphogenesis, allowing us to infer developmental steps by which they form. First, we found that the sheath glial cell begins wrapping its partner neurons at the distal tip of the dendrites where it self-fuses into a seamless tube and then “zippers” down the dendrite. In many cases, sheath glia wrap the progenitors of partner neurons prior to their terminal division. After sheath wrapping has begun, the socket glia wraps the sheath glia circumferentially before presumably elongating to form the mature sheath–socket channel. We also observed transient interactions not found in the mature animal, such as amphid sheath glia wrapping the AUA neuron, that may reflect ancestral relationships. This study demonstrates the value of large public EM datasets that can be mined for new insights and sheds light on how neurons and glia undergo coordinated morphogenesis.</p>","PeriodicalId":15552,"journal":{"name":"Journal of Comparative Neurology","volume":"533 9","pages":""},"PeriodicalIF":2.1000,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cne.70084","citationCount":"0","resultStr":"{\"title\":\"Embryonic Development of Caenorhabditis elegans Sense Organs\",\"authors\":\"Leland R. Wexler,&nbsp;Irina Kolotuev,&nbsp;Maxwell G. Heiman\",\"doi\":\"10.1002/cne.70084\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><i>Caenorhabditis elegans</i> sense organs provide a powerful model for understanding how different cell types interact to assemble a functional organ. Each sense organ is composed of two glial cells, called the sheath and socket, and one or more neurons. A major challenge in studying their development has been the lack of methods to directly observe these structures in the embryo. Here, we mine a recently published high-resolution ultrastructural dataset of a comma-stage embryo that provides an untapped resource for visualizing early developmental events. From this dataset, we reconstructed all head sense organs (two amphid [AM], four cephalic [CEP], six inner labial [IL], four outer labial quadrant [OLQ], and two outer labial lateral [OLL]). Symmetric sense organs were at different stages of morphogenesis, allowing us to infer developmental steps by which they form. First, we found that the sheath glial cell begins wrapping its partner neurons at the distal tip of the dendrites where it self-fuses into a seamless tube and then “zippers” down the dendrite. In many cases, sheath glia wrap the progenitors of partner neurons prior to their terminal division. After sheath wrapping has begun, the socket glia wraps the sheath glia circumferentially before presumably elongating to form the mature sheath–socket channel. We also observed transient interactions not found in the mature animal, such as amphid sheath glia wrapping the AUA neuron, that may reflect ancestral relationships. This study demonstrates the value of large public EM datasets that can be mined for new insights and sheds light on how neurons and glia undergo coordinated morphogenesis.</p>\",\"PeriodicalId\":15552,\"journal\":{\"name\":\"Journal of Comparative Neurology\",\"volume\":\"533 9\",\"pages\":\"\"},\"PeriodicalIF\":2.1000,\"publicationDate\":\"2025-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cne.70084\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Comparative Neurology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/cne.70084\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"NEUROSCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Comparative Neurology","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cne.70084","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

摘要

秀丽隐杆线虫的感觉器官为理解不同类型的细胞如何相互作用以组装一个功能器官提供了一个强大的模型。每个感觉器官由两个神经胶质细胞(鞘和窝)和一个或多个神经元组成。研究它们发育的一个主要挑战是缺乏在胚胎中直接观察这些结构的方法。在这里,我们挖掘了最近发表的逗号阶段胚胎的高分辨率超微结构数据集,为可视化早期发育事件提供了尚未开发的资源。从这个数据集中,我们重建了所有的头部感觉器官(2个双侧[AM], 4个头侧[CEP], 6个内唇[IL], 4个外唇象限[OLQ]和2个外唇外侧[OLL])。对称感觉器官处于形态发生的不同阶段,这使我们能够推断它们形成的发育步骤。首先,我们发现鞘状胶质细胞开始在树突远端包裹它的伙伴神经元,在那里它自我融合成一个无缝管,然后“拉链”沿着树突向下延伸。在许多情况下,在伴侣神经元的末梢分裂之前,鞘胶质包裹着它们的祖细胞。鞘包裹开始后,窝状胶质细胞向周向包裹鞘状胶质细胞,然后可能伸长形成成熟的鞘-窝通道。我们还观察到在成熟动物中没有发现的短暂相互作用,例如两栖动物鞘胶质包裹着AUA神经元,这可能反映了祖先的关系。这项研究证明了大型公共EM数据集的价值,这些数据集可以挖掘新的见解,并揭示神经元和胶质细胞如何经历协调的形态发生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Embryonic Development of Caenorhabditis elegans Sense Organs

Embryonic Development of Caenorhabditis elegans Sense Organs

Caenorhabditis elegans sense organs provide a powerful model for understanding how different cell types interact to assemble a functional organ. Each sense organ is composed of two glial cells, called the sheath and socket, and one or more neurons. A major challenge in studying their development has been the lack of methods to directly observe these structures in the embryo. Here, we mine a recently published high-resolution ultrastructural dataset of a comma-stage embryo that provides an untapped resource for visualizing early developmental events. From this dataset, we reconstructed all head sense organs (two amphid [AM], four cephalic [CEP], six inner labial [IL], four outer labial quadrant [OLQ], and two outer labial lateral [OLL]). Symmetric sense organs were at different stages of morphogenesis, allowing us to infer developmental steps by which they form. First, we found that the sheath glial cell begins wrapping its partner neurons at the distal tip of the dendrites where it self-fuses into a seamless tube and then “zippers” down the dendrite. In many cases, sheath glia wrap the progenitors of partner neurons prior to their terminal division. After sheath wrapping has begun, the socket glia wraps the sheath glia circumferentially before presumably elongating to form the mature sheath–socket channel. We also observed transient interactions not found in the mature animal, such as amphid sheath glia wrapping the AUA neuron, that may reflect ancestral relationships. This study demonstrates the value of large public EM datasets that can be mined for new insights and sheds light on how neurons and glia undergo coordinated morphogenesis.

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
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