AI Article Synopsis

  • Biomedical imaging tools, like light and electron microscopy, help study gene functions in Drosophila melanogaster, enhancing our understanding from cells to entire organisms.
  • A new method using microcomputed tomography (µ-CT) enables visualization of Drosophila at any developmental stage without the need for invasive techniques, producing precise 3D information.
  • Combining µ-CT with other imaging platforms allows for detailed analysis of tissues and organs, improving our ability to explore genetic mechanisms in development, physiology, and anatomy.

Article Abstract

Biomedical imaging tools permit investigation of molecular mechanisms across spatial scales, from genes to organisms. Drosophila melanogaster, a well-characterized model organism, has benefited from the use of light and electron microscopy to understand gene function at the level of cells and tissues. The application of imaging platforms that allow for an understanding of gene function at the level of the entire intact organism would further enhance our knowledge of genetic mechanisms. Here a whole animal imaging method is presented that outlines the steps needed to visualize Drosophila at any developmental stage using microcomputed tomography (µ-CT). The advantages of µ-CT include commercially available instrumentation and minimal hands-on time to produce accurate 3D information at micron-level resolution without the need for tissue dissection or clearing methods. Paired with software that accelerate image analysis and 3D rendering, detailed morphometric analysis of any tissue or organ system can be performed to better understand mechanisms of development, physiology, and anatomy for both descriptive and hypothesis testing studies. By utilizing an imaging workflow that incorporates the use of electron microscopy, light microscopy, and µ-CT, a thorough evaluation of gene function can be performed, thus furthering the usefulness of this powerful model organism.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7891681PMC
http://dx.doi.org/10.3791/61515DOI Listing

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