| Autor: |
Strobl F; Physical Biology, Buchmann Institute for Molecular Life Sciences (BMLS); Cluster of Excellence Frankfurt, Macromolecular Complexes; Goethe-Universität Frankfurt am Main - Campus Riedberg., Klees S; Physical Biology, Buchmann Institute for Molecular Life Sciences (BMLS); Cluster of Excellence Frankfurt, Macromolecular Complexes; Goethe-Universität Frankfurt am Main - Campus Riedberg., Stelzer EHK; Physical Biology, Buchmann Institute for Molecular Life Sciences (BMLS); Cluster of Excellence Frankfurt, Macromolecular Complexes; Goethe-Universität Frankfurt am Main - Campus Riedberg; ernst.stelzer@physikalischebiologie.de. |
| Jazyk: |
angličtina |
| Zdroj: |
Journal of visualized experiments : JoVE [J Vis Exp] 2017 Apr 28 (122). Date of Electronic Publication: 2017 Apr 28. |
| DOI: |
10.3791/55629 |
| Abstrakt: |
The red flour beetle Tribolium castaneum has become an important insect model organism in developmental genetics and evolutionary developmental biology. The observation of Tribolium embryos with light sheet-based fluorescence microscopy has multiple advantages over conventional widefield and confocal fluorescence microscopy. Due to the unique properties of a light sheet-based microscope, three dimensional images of living specimens can be recorded with high signal-to-noise ratios and significantly reduced photo-bleaching as well as photo-toxicity along multiple directions over periods that last several days. With more than four years of methodological development and a continuous increase of data, the time seems appropriate to establish standard operating procedures for the usage of light sheet technology in the Tribolium community as well as in the insect community at large. This protocol describes three mounting techniques suitable for different purposes, presents two novel custom-made transgenic Tribolium lines appropriate for long-term live imaging, suggests five fluorescent dyes to label intracellular structures of fixed embryos and provides information on data post-processing for the timely evaluation of the recorded data. Representative results concentrate on long-term live imaging, optical sectioning and the observation of the same embryo along multiple directions. The respective datasets are provided as a downloadable resource. Finally, the protocol discusses quality controls for live imaging assays, current limitations and the applicability of the outlined procedures to other insect species. This protocol is primarily intended for developmental biologists who seek imaging solutions that outperform standard laboratory equipment. It promotes the continuous attempt to close the gap between the technically orientated laboratories/communities, which develop and refine microscopy methodologically, and the life science laboratories/communities, which require 'plug-and-play' solutions to technical challenges. Furthermore, it supports an axiomatic approach that moves the biological questions into the center of attention. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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