A simple method for long-term vital-staining of ciliated epidermal cells in aquatic larvae.

Journal of biological methods Pub Date : 2020-04-29 eCollection Date: 2020-01-01 DOI:10.14440/jbm.2020.320
Jörn von Döhren, Sabrina Kuhl
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Abstract

Observing the process of growth and differentiation of tissues and organs is of crucial importance for the understanding of the evolution of organs in animals. Unfortunately, it is notoriously difficult to continuously monitor developmental processes due to the extended time they take. Long-term labeling of the tissues of interest represents a promising alternative to raise these pivotal data. In the case of the prototroch, a band of ciliated cells typical of marine, planktotrophic trochophora larvae, we were able to apply a long-term fluorescent vital-staining to the prototroch cells that remains detectable throughout further larval life. We were able to stain ciliated cells of planktonic larvae from different spiralian clades by using long-chain dialkylcarbocyanine dyes that are detectable in different fluorescent emission spectra in combination with a non-ionic surfactant. The larvae survived and developed normally, their ciliated cells retaining the originally applied fluorescent labels. Combined with additional fluorescent staining of the larvae after fixation, we provide an easy, versatile, and broadly applicable method to investigate the processes of the differentiation of epidermal organs in various aquatic larvae.

Abstract Image

Abstract Image

Abstract Image

水生幼虫纤毛表皮细胞长期活体染色的简单方法。
观察组织器官的生长和分化过程对认识动物器官的进化具有重要意义。不幸的是,持续监控开发过程是非常困难的,因为它们需要花费很长的时间。对感兴趣的组织进行长期标记是提高这些关键数据的一个有希望的替代方法。在原滋养体的情况下,一束典型的海洋纤毛细胞,浮游营养型trochophora幼虫,我们能够对原滋养体细胞应用长期荧光生命染色,在幼虫的进一步生命中仍然可以检测到。我们利用长链二烷基碳菁染料与非离子表面活性剂结合,在不同的荧光发射光谱中可检测到,从而能够对不同螺旋体分支浮游生物幼虫的纤毛细胞进行染色。幼虫存活并正常发育,其纤毛细胞保留了最初应用的荧光标记。结合固定后幼虫的附加荧光染色,我们提供了一种简单、通用、广泛适用的方法来研究各种水生幼虫表皮器官的分化过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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