Game-changing new technique

This image is a composition of snap shots from a time lapse video of a closing wound in the epidermis of a Drosophila larvae. The cells express two fluorescently labelled markers: a PIP3 sensor (green) and the myosin light chain (magenta). Credit: Parisa Kakanj/EMBL

Monitoring organs and cells in living fly larvae

Small changes in a cell’s composition can radically transform its function and drive the development of diseases like diabetes, cancer, or neuronal dysfunction. Scientists led by the European Molecular Biology Laboratory in Heidelberg, the Institute for Genetics of the University of Cologne, the Max Planck Institute for Biology of Ageing, and CECAD and the CMMC in Cologne have developed a method to study processes taking place in the cells of a living fruit fly larva. This technique, published in Nature Protocols on 10 February, provides a simple but effective way to study the functions of organs in living animals.

For decades, scientists have been using the fruit fly Drosophila to understand biological processes. Key biological processes and 60% of fruit fly genes are also seen in humans, having been evolutionarily conserved. The fruit fly is therefore a powerful model organism for studying genetics. Scientists have created many genetic tools and techniques to study molecular processes of development and human disease in the fruit fly.

The challenge

Most previous studies have been carried out in the Drosophila embryo or in adult flies, but the fruit fly larva also offers enormous research potential. Its transparent body, with highly developed functional organs including brain, gut, and muscle, makes the larva an excellent system for observing the dynamics of cellular and molecular processes in living animals.

“The cells in a fruit fly larva are much bigger than in the embryo. You can see all organelles and even the subcellular processes. That's the beauty of the system,” says Parisa Kakanj, the scientist who led the study in Germany.

However, the larva’s continuous crawling makes live monitoring a challenge, and some cellular processes only reveal their secrets through long-term imaging. Kakanj, a researcher in the groups of Maria Leptin and Linda Partridge, tackled this challenge and developed a method for simple immobilisation of the larvae that allows long-term live imaging and the investigation of cellular events at high resolution.

Simple, fast, and efficient

In the past, scientists have used mechanical methods or anaesthetics to tranquilize fruit fly larvae. Both approaches had undesired side-effects, such as mechanical pressure, limited immobilisation, and high mortality. Further, simultaneous screening of many larvae was impossible.

“In contrast to previous techniques, we developed a simple method for short-term treatment with ether, a classical anaesthetic. This approach allowed undisrupted long-term immobilisation of many larvae in parallel,” explains Parisa Kakanj.

A promising model for drug discovery

To prove the technique's capabilities, the team investigated wound healing in larvae. They examined the influence of insulin and TOR – crucial signalling molecules for cell survival, growth, and proliferation – on this process. By studying the subcellular dynamics, the scientists created a temporal map of insulin and TOR pathway activity during wound closure. They found that lowering insulin signalling at the wound edge slows down the healing process.

Long-term in vivo imaging, coupled with genetic manipulations, opens the path to many aspects of biology and physiology. “This technique will help many scientists studying neuronal signalling, fat metabolism, or tumour formation, and will provide new opportunities for drug discovery,” says Parisa Kakanj.

Original Publication
Parisa Kakanj, Sabine A. Eming, Linda Partridge, Maria Leptin
Long-term in vivo imaging of Drosophila larvae.
Nature Protocols, 10 February 2020. DOI: 10.1038/s41596-019-0282-z

This press release was provided by EMBL.

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