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JoVE Journal
Biology
Gleichzeitige Live-Bildgebung mehrerer Insektenembryonen in probenkammerbasierten Lichtbogenfluor...
Gleichzeitige Live-Bildgebung mehrerer Insektenembryonen in probenkammerbasierten Lichtbogenfluor...
JoVE Journal
Biology
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JoVE Journal Biology
Simultaneous Live Imaging of Multiple Insect Embryos in Sample Chamber-Based Light Sheet Fluorescence Microscopes

Gleichzeitige Live-Bildgebung mehrerer Insektenembryonen in probenkammerbasierten Lichtbogenfluoreszenzmikroskopen

Full Text
3,577 Views
08:29 min
September 9, 2020

DOI: 10.3791/61713-v

Julia Ratke*1, Franziska Krämer*1, Frederic Strobl1

1Physical Biology/Physikalische Biologie (IZN, FB15), Buchmann Institute for Molecular Life Sciences (BMLS), Cluster of Excellence Frankfurt, Macromolecular Complexes (CEF - MC),Goethe-Universität

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Overview

This study presents a protocol for simultaneous live imaging of multiple specimens using light sheet-based fluorescence microscopy, addressing issues of ambient variance in developmental biology. By utilizing a cobweb holder for stacking embryos, the method enhances the efficacy of imaging while minimizing inconsistencies.

Key Study Components

Research Area

  • Developmental biology
  • Fluorescence microscopy
  • Live imaging techniques

Background

  • The importance of minimizing ambient variance in comparative studies.
  • Challenges associated with sequential live imaging assays.
  • Need for innovative methods that improve throughput and accuracy in imaging.

Methods Used

  • Use of cobweb holder for simultaneous embryo imaging
  • Embryo mounting and dechorionation protocols
  • Live imaging calibration using agarose and fluorescent microspheres

Main Results

  • Successful simultaneous imaging of multiple embryos.
  • Reduced ambient variance leading to clearer imaging results.
  • Instructional video to guide correct mounting and imaging steps.

Conclusions

  • This study demonstrates a new protocol that significantly improves the live imaging process in developmental biology.
  • The relevance of the findings may enhance future research methodologies and outcomes in comparative studies.

Frequently Asked Questions

What is the significance of reducing ambient variance in imaging?
Reducing ambient variance enhances the accuracy and consistency of imaging results in developmental biology studies.
How does the cobweb holder improve throughput?
The cobweb holder allows for stacking multiple embryos, enabling simultaneous imaging rather than sequential, which increases efficiency.
What preparation steps are required for embryo dechorionation?
Embryos are washed using autoclaved tap water and sodium hypochlorite solution to remove chorions before imaging.
Is there a video tutorial associated with the protocol?
Yes, an instructional video is provided to illustrate the key procedures and tips for successful embryo mounting and imaging.
What organism is primarily used in this study?
The study primarily uses embryos from transgenic Drosophila lines for live imaging assays.
What technologies are employed in the imaging process?
Light sheet fluorescence microscopy and agarose embedding techniques are employed in the imaging process.
How does imaging contribute to developmental biology research?
Imaging allows researchers to observe and analyze developmental processes in real-time, providing insights into genetic and cellular mechanisms.

Die Lichtbogen-basierte Fluoreszenzmikroskopie ist das wertvollste Werkzeug in der Entwicklungsbiologie. Ein wichtiges Thema in vergleichenden Studien ist die Varianz der Umgebung. Unser Protokoll beschreibt ein experimentelles Framework für die gleichzeitige Live-Bildgebung mehrerer Proben und befasst sich daher proaktiv mit diesem Problem.

Probenkammerbasierte Lichtblatt-Floreszenzmikroskope sind eher für einen hohen Gehalt als für einen hohen Durchsatz ausgelegt. Live-Imaging-Assays müssen daher sequentiell durchgeführt werden und werden daher weniger von der Umgebungsvarianz beeinflusst. Unsere Spinnwebenhalter ermöglichen das Stapeln und gleichzeitige Imaging mehrerer Embryonen, wodurch Umgebungsschwankungen eliminiert und der Durchsatz erhöht werden.

Das Einsetzen von Embryonen in den Spinnwebenhalter erfordert eine gewisse Fingerspitzengefühl. Ein Erklärvideo eignet sich ideal, um die Abfolge der vielen kurzen Verhaltensgesten zu veranschaulichen. Zur Kalibrierung des Probenkammer-basierten Lichtblatt-Fluoreszenzmikroskops.

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Biologie Ausgabe 163 vergleichende Live-Bildgebung simultane Live-Bildgebung dreidimensionale Lichtmikroskopie Lichtblatt-basierte Fluoreszenzmikroskopie LSFM Spinnwebenhalter Insektenentwicklung embryonale Morphogenese Embryogenese Drosophila melanogaster Tribolium castaneum Umgebungsvarianz

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