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
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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。
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.

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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.
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