Literature DB >> 28518097

Light Sheet-based Fluorescence Microscopy of Living or Fixed and Stained Tribolium castaneum Embryos.

Frederic Strobl1, Selina Klees1, Ernst H K Stelzer2.   

Abstract

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.

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Year:  2017        PMID: 28518097      PMCID: PMC5565123          DOI: 10.3791/55629

Source DB:  PubMed          Journal:  J Vis Exp        ISSN: 1940-087X            Impact factor:   1.355


  109 in total

Review 1.  Use of the piggyBac transposon for germ-line transformation of insects.

Authors:  Alfred M Handler
Journal:  Insect Biochem Mol Biol       Date:  2002-10       Impact factor: 4.714

2.  Quantitative high-speed imaging of entire developing embryos with simultaneous multiview light-sheet microscopy.

Authors:  Raju Tomer; Khaled Khairy; Fernando Amat; Philipp J Keller
Journal:  Nat Methods       Date:  2012-06-03       Impact factor: 28.547

3.  The extraembryonic serosa protects the insect egg against desiccation.

Authors:  Chris G C Jacobs; Gustavo L Rezende; Gerda E M Lamers; Maurijn van der Zee
Journal:  Proc Biol Sci       Date:  2013-06-19       Impact factor: 5.349

4.  Light-sheet fluorescence microscopy for quantitative biology.

Authors:  Ernst H K Stelzer
Journal:  Nat Methods       Date:  2015-01       Impact factor: 28.547

5.  Germline transformation of the silkworm Bombyx mori L. using a piggyBac transposon-derived vector.

Authors:  T Tamura; C Thibert; C Royer; T Kanda; E Abraham; M Kamba; N Komoto; J L Thomas; B Mauchamp; G Chavancy; P Shirk; M Fraser; J C Prudhomme; P Couble; T Toshiki; T Chantal; R Corinne; K Toshio; A Eappen; K Mari; K Natuo; T Jean-Luc; M Bernard; C Gérard; S Paul; F Malcolm; P Jean-Claude; C Pierre
Journal:  Nat Biotechnol       Date:  2000-01       Impact factor: 54.908

6.  Tubulin superfamily genes in Tribolium castaneum and the use of a Tubulin promoter to drive transgene expression.

Authors:  Kendra S Siebert; Marcé D Lorenzen; Susan J Brown; Yoonseong Park; Richard W Beeman
Journal:  Insect Biochem Mol Biol       Date:  2008-05-16       Impact factor: 4.714

7.  Efficient transformation of the beetle Tribolium castaneum using the Minos transposable element: quantitative and qualitative analysis of genomic integration events.

Authors:  Anastasios Pavlopoulos; Andreas J Berghammer; Michalis Averof; Martin Klingler
Journal:  Genetics       Date:  2004-06       Impact factor: 4.562

8.  Large-scale insertional mutagenesis of a coleopteran stored grain pest, the red flour beetle Tribolium castaneum, identifies embryonic lethal mutations and enhancer traps.

Authors:  Jochen Trauner; Johannes Schinko; Marcé D Lorenzen; Teresa D Shippy; Ernst A Wimmer; Richard W Beeman; Martin Klingler; Gregor Bucher; Susan J Brown
Journal:  BMC Biol       Date:  2009-11-05       Impact factor: 7.431

9.  Fast, high-contrast imaging of animal development with scanned light sheet-based structured-illumination microscopy.

Authors:  Philipp J Keller; Annette D Schmidt; Anthony Santella; Khaled Khairy; Zhirong Bao; Joachim Wittbrodt; Ernst H K Stelzer
Journal:  Nat Methods       Date:  2010-07-04       Impact factor: 28.547

10.  High plasticity in epithelial morphogenesis during insect dorsal closure.

Authors:  Kristen A Panfilio; Georg Oberhofer; Siegfried Roth
Journal:  Biol Open       Date:  2013-09-05       Impact factor: 2.422

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  8 in total

1.  A universal vector concept for a direct genotyping of transgenic organisms and a systematic creation of homozygous lines.

Authors:  Frederic Strobl; Anita Anderl; Ernst Hk Stelzer
Journal:  Elife       Date:  2018-03-15       Impact factor: 8.140

2.  Non-lethal genotyping of Tribolium castaneum adults using genomic DNA extracted from wing tissue.

Authors:  Frederic Strobl; J Alexander Ross; Ernst H K Stelzer
Journal:  PLoS One       Date:  2017-08-11       Impact factor: 3.240

Review 3.  Fluorescence Microscopy-An Outline of Hardware, Biological Handling, and Fluorophore Considerations.

Authors:  Shane M Hickey; Ben Ung; Christie Bader; Robert Brooks; Joanna Lazniewska; Ian R D Johnson; Alexandra Sorvina; Jessica Logan; Carmela Martini; Courtney R Moore; Litsa Karageorgos; Martin J Sweetman; Douglas A Brooks
Journal:  Cells       Date:  2021-12-23       Impact factor: 6.600

4.  Light sheet fluorescence microscopy for the investigation of blood-sucking arthropods dyed via artificial membrane feeding.

Authors:  Lars Ten Bosch; Birgit Habedank; Alessia Candeo; Andrea Bassi; Gianluca Valentini; Christoph Gerhard
Journal:  Parasit Vectors       Date:  2022-02-12       Impact factor: 3.876

5.  QuickPIV: Efficient 3D particle image velocimetry software applied to quantifying cellular migration during embryogenesis.

Authors:  Marc Pereyra; Armin Drusko; Franziska Krämer; Frederic Strobl; Ernst H K Stelzer; Franziska Matthäus
Journal:  BMC Bioinformatics       Date:  2021-12-04       Impact factor: 3.169

6.  In toto light sheet fluorescence microscopy live imaging datasets of Ceratitis capitata embryonic development.

Authors:  Frederic Strobl; Marc F Schetelig; Ernst H K Stelzer
Journal:  Sci Data       Date:  2022-06-15       Impact factor: 8.501

7.  An ancestral apical brain region contributes to the central complex under the control of foxQ2 in the beetle Tribolium.

Authors:  Bicheng He; Marita Buescher; Max Stephen Farnworth; Frederic Strobl; Ernst Hk Stelzer; Nikolaus Db Koniszewski; Dominik Muehlen; Gregor Bucher
Journal:  Elife       Date:  2019-10-18       Impact factor: 8.140

8.  A deterministic genotyping workflow reduces waste of transgenic individuals by two-thirds.

Authors:  Frederic Strobl; Ernst H K Stelzer
Journal:  Sci Rep       Date:  2021-07-28       Impact factor: 4.379

  8 in total

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