利用共聚焦显微镜量化离体珊瑚细胞中的细胞膜 "游离 "钙。

IF 2.8 2区 生物学 Q2 BIOLOGY Journal of Experimental Biology Pub Date : 2024-10-01 Epub Date: 2024-10-04 DOI:10.1242/jeb.247638
Alexander A Venn, Nathalie Techer, Natacha Segonds, Eric Tambutté, Sylvie Tambutté
{"title":"利用共聚焦显微镜量化离体珊瑚细胞中的细胞膜 \"游离 \"钙。","authors":"Alexander A Venn, Nathalie Techer, Natacha Segonds, Eric Tambutté, Sylvie Tambutté","doi":"10.1242/jeb.247638","DOIUrl":null,"url":null,"abstract":"<p><p>Despite its prominent role as an intracellular messenger in all organisms, cytosolic free calcium ([Ca2+]i) has never been quantified in corals or cnidarians in general. Ratiometric calcium dyes and cell imaging have been key methods in successful research on [Ca2+]i in model systems, and could be applied to corals. Here, we developed a procedure to quantify [Ca2+]i in isolated cells from the model coral species Stylophora pistillata using Indo-1 and confocal microscopy. We quantified [Ca2+]i in coral cells with and without intracellular dinoflagellate symbionts, and verified our procedure on cultured mammalian cells. We then used our procedure to measure changes in [Ca2+]i in coral cells exposed to a classic inhibitor of [Ca2+]i regulation, thapsigargin, and also used it to record elevations in [Ca2+]i in coral cells undergoing apoptosis. Our procedure paves the way for future studies into intracellular calcium in corals and other cnidarians.</p>","PeriodicalId":15786,"journal":{"name":"Journal of Experimental Biology","volume":null,"pages":null},"PeriodicalIF":2.8000,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Quantification of cytosolic 'free' calcium in isolated coral cells with confocal microscopy.\",\"authors\":\"Alexander A Venn, Nathalie Techer, Natacha Segonds, Eric Tambutté, Sylvie Tambutté\",\"doi\":\"10.1242/jeb.247638\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Despite its prominent role as an intracellular messenger in all organisms, cytosolic free calcium ([Ca2+]i) has never been quantified in corals or cnidarians in general. Ratiometric calcium dyes and cell imaging have been key methods in successful research on [Ca2+]i in model systems, and could be applied to corals. Here, we developed a procedure to quantify [Ca2+]i in isolated cells from the model coral species Stylophora pistillata using Indo-1 and confocal microscopy. We quantified [Ca2+]i in coral cells with and without intracellular dinoflagellate symbionts, and verified our procedure on cultured mammalian cells. We then used our procedure to measure changes in [Ca2+]i in coral cells exposed to a classic inhibitor of [Ca2+]i regulation, thapsigargin, and also used it to record elevations in [Ca2+]i in coral cells undergoing apoptosis. Our procedure paves the way for future studies into intracellular calcium in corals and other cnidarians.</p>\",\"PeriodicalId\":15786,\"journal\":{\"name\":\"Journal of Experimental Biology\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":2.8000,\"publicationDate\":\"2024-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Experimental Biology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1242/jeb.247638\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/10/4 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q2\",\"JCRName\":\"BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Experimental Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1242/jeb.247638","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/10/4 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"BIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

尽管细胞游离钙([Ca2+]i)作为细胞内信使在所有生物中都发挥着重要作用,但在珊瑚或一般的刺胞动物中却从未被量化过。比率钙染料和细胞成像是成功研究模式系统中[Ca2+]i的关键方法,也可应用于珊瑚。在此,我们开发了一套程序,利用 Indo-1 和共聚焦显微镜量化模式珊瑚物种 Stylophora pistillata 分离细胞中的 [Ca2+]i。我们量化了有和没有胞内甲藻共生体的珊瑚细胞中的[Ca2+]i,并在培养的哺乳动物细胞上验证了我们的程序。然后,我们用我们的方法测量了暴露于[Ca2+]i调节的典型抑制剂--thapsigargin的珊瑚细胞中[Ca2+]i的变化,还用它记录了发生凋亡的珊瑚细胞中[Ca2+]i的升高。我们的方法为今后研究珊瑚和其他刺胞动物的细胞内钙铺平了道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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
Quantification of cytosolic 'free' calcium in isolated coral cells with confocal microscopy.

Despite its prominent role as an intracellular messenger in all organisms, cytosolic free calcium ([Ca2+]i) has never been quantified in corals or cnidarians in general. Ratiometric calcium dyes and cell imaging have been key methods in successful research on [Ca2+]i in model systems, and could be applied to corals. Here, we developed a procedure to quantify [Ca2+]i in isolated cells from the model coral species Stylophora pistillata using Indo-1 and confocal microscopy. We quantified [Ca2+]i in coral cells with and without intracellular dinoflagellate symbionts, and verified our procedure on cultured mammalian cells. We then used our procedure to measure changes in [Ca2+]i in coral cells exposed to a classic inhibitor of [Ca2+]i regulation, thapsigargin, and also used it to record elevations in [Ca2+]i in coral cells undergoing apoptosis. Our procedure paves the way for future studies into intracellular calcium in corals and other cnidarians.

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
5.50
自引率
10.70%
发文量
494
审稿时长
1 months
期刊介绍: Journal of Experimental Biology is the leading primary research journal in comparative physiology and publishes papers on the form and function of living organisms at all levels of biological organisation, from the molecular and subcellular to the integrated whole animal.
期刊最新文献
How do fish miss? Attack strategies of threespine stickleback capturing non-evasive prey. Hypertonic water reabsorption with a parallel-current system via the glandular and saccular renal tubules of Ruditapes philippinarum. Skittering locomotion in cricket frogs: a form of porpoising. Investigating in vivo force and work production of rat medial gastrocnemius at varying locomotor speeds using a muscle avatar. Bridging the divide in organismal physiology: a case for the integration of behaviour as a physiological process.
×
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