Shear stress sensing in C. elegans.

IF 8.1 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Current Biology Pub Date : 2024-11-18 Epub Date: 2024-10-28 DOI:10.1016/j.cub.2024.09.075
Zhiyong Zhang, Xia Li, Can Wang, Fengfan Zhang, Jianfeng Liu, X Z Shawn Xu
{"title":"Shear stress sensing in C. elegans.","authors":"Zhiyong Zhang, Xia Li, Can Wang, Fengfan Zhang, Jianfeng Liu, X Z Shawn Xu","doi":"10.1016/j.cub.2024.09.075","DOIUrl":null,"url":null,"abstract":"<p><p>Shear stress sensing represents a vital mode of mechanosensation.<sup>1</sup> Previous efforts have mainly focused on characterizing how various cell types-for example, vascular endothelial cells-sense shear stress arising from fluid flow within the animal body.<sup>1</sup><sup>,</sup><sup>2</sup> How animals sense shear stress derived from their external environment, however, is not well understood. Here, using C. elegans as a model, we show that external fluid flow triggers behavioral responses in C. elegans, facilitating their navigation of the environment during swimming. Such behavioral responses primarily result from shear stress generated by fluid flow. The sensory neurons AWC, ASH, and ASER are the major shear stress-sensitive neurons, among which AWC shows the most robust response to shear stress and is required for shear stress-induced behavior. Mechanistically, shear stress signals are transduced by G protein signaling in AWC, with cGMP as the second messenger, culminating in the opening of cGMP-sensitive cyclic nucleotide-gated (CNG) channels and neuronal excitation. These studies demonstrate that C. elegans senses and responds to shear stress and characterize the underlying neural and molecular mechanisms. Our work helps establish C. elegans as a genetic model for studying shear stress sensing.</p>","PeriodicalId":11359,"journal":{"name":"Current Biology","volume":" ","pages":"5382-5391.e3"},"PeriodicalIF":8.1000,"publicationDate":"2024-11-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11576262/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1016/j.cub.2024.09.075","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/10/28 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Shear stress sensing represents a vital mode of mechanosensation.1 Previous efforts have mainly focused on characterizing how various cell types-for example, vascular endothelial cells-sense shear stress arising from fluid flow within the animal body.1,2 How animals sense shear stress derived from their external environment, however, is not well understood. Here, using C. elegans as a model, we show that external fluid flow triggers behavioral responses in C. elegans, facilitating their navigation of the environment during swimming. Such behavioral responses primarily result from shear stress generated by fluid flow. The sensory neurons AWC, ASH, and ASER are the major shear stress-sensitive neurons, among which AWC shows the most robust response to shear stress and is required for shear stress-induced behavior. Mechanistically, shear stress signals are transduced by G protein signaling in AWC, with cGMP as the second messenger, culminating in the opening of cGMP-sensitive cyclic nucleotide-gated (CNG) channels and neuronal excitation. These studies demonstrate that C. elegans senses and responds to shear stress and characterize the underlying neural and molecular mechanisms. Our work helps establish C. elegans as a genetic model for studying shear stress sensing.

秀丽隐杆线虫的剪切应力感应
剪切应力感应是机械感应的一种重要模式1 。以前的研究主要集中在描述各种细胞类型--例如血管内皮细胞--如何感应动物体内流体流动产生的剪切应力1,2 。在这里,我们以 elegans 为模型,证明外部流体流动会触发 elegans 的行为反应,从而促进它们在游泳过程中对环境的导航。这种行为反应主要源于流体流动产生的剪切应力。感觉神经元 AWC、ASH 和 ASER 是对剪切应力敏感的主要神经元,其中 AWC 对剪切应力的反应最为强烈,是剪切应力诱导行为所必需的神经元。从机理上讲,剪切应力信号通过 AWC 中的 G 蛋白信号转导,以 cGMP 为第二信使,最终导致对 cGMP 敏感的环核苷酸门控(CNG)通道开放和神经元兴奋。这些研究证明了秀丽隐杆线虫能感知剪切应力并对其做出反应,并描述了其潜在的神经和分子机制。我们的工作有助于将 elegans 确立为研究剪切应力感应的遗传模型。
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
Current Biology
Current Biology 生物-生化与分子生物学
CiteScore
11.80
自引率
2.20%
发文量
869
审稿时长
46 days
期刊介绍: Current Biology is a comprehensive journal that showcases original research in various disciplines of biology. It provides a platform for scientists to disseminate their groundbreaking findings and promotes interdisciplinary communication. The journal publishes articles of general interest, encompassing diverse fields of biology. Moreover, it offers accessible editorial pieces that are specifically designed to enlighten non-specialist readers.
×
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