Ji Hui, Han Chun
Weill Institute for Cell and Molecular Biology and Department of Molecular Biology and Genetics, Cornell University.
Weill Institute for Cell and Molecular Biology and Department of Molecular Biology and Genetics, Cornell University;
J Vis Exp. 2020 Feb 27(156). doi: 10.3791/60792.
Live imaging is a valuable approach for investigating cell biology questions. The Drosophila larva is particularly suited for in vivo live imaging because the larval body wall and most internal organs are transparent. However, continuous live imaging of intact Drosophila larvae for longer than 30 min has been challenging because it is difficult to noninvasively immobilizeimmobilizing larvae for a long time. Here we present a larval mounting method called LarvaSPA that allows for continuous imaging of live Drosophila larvae with high temporal and spatial resolution for longer than 10 hours. This method involves partially attaching larvae to the coverslip using a UV-reactive glue and additionally restraining larval movement using a polydimethylsiloxane (PDMS) block. This method is compatible with larvae at developmental stages from second instar to wandering third instar. We demonstrate applications of this method in studying dynamic processes of Drosophila somatosensory neurons, including dendrite growth and injury-induced dendrite degeneration. This method can also be applied to study many other cellular processes that happen near the larval body wall.
实时成像技术是研究细胞生物学问题的一种重要方法。果蝇幼虫特别适合用于体内实时成像,因为幼虫的体壁和大多数内部器官都是透明的。然而,对完整的果蝇幼虫进行超过30分钟的连续实时成像一直具有挑战性,因为很难长时间非侵入性地固定幼虫。在这里,我们介绍一种称为LarvaSPA的幼虫固定方法,该方法能够以高时空分辨率对活的果蝇幼虫进行超过10小时的连续成像。该方法包括使用紫外线反应性胶水将幼虫部分附着在盖玻片上,并使用聚二甲基硅氧烷(PDMS)块进一步限制幼虫的运动。此方法适用于从二龄到三龄漫游期的各发育阶段的幼虫。我们展示了该方法在研究果蝇体感神经元动态过程中的应用,包括树突生长和损伤诱导的树突退化。该方法还可用于研究幼虫体壁附近发生的许多其他细胞过程。