Dissection and Direct Imaging of Axonal Transport in Drosophila Segmental Nerves.

Methods Mol Biol

Department of Molecular, Cell and Developmental Biology, University of California Santa Cruz, Santa Cruz, CA, USA.

Published: April 2022

AI Article Synopsis

  • Cytoskeletal motors are essential for transporting mitochondria and other components in neurons, especially those with long axons, as defects can severely impair their function.
  • A mutation in the gene for kinesin-1 can lead to serious conditions like spastic paraplegia due to its role in axonal transport.
  • Researchers utilized Drosophila to develop a new imaging technique to observe organelle transport in long motor axons, enabling better study of the proteins involved in these processes.

Article Abstract

For neurons, especially those with long axons, the forceful transport of mitochondria, vesicles, and other cytoplasmic components by cytoskeletal motors is vital. Defects in cytoplasmic transport machinery cause a degradation of signaling capacity that is most severe for neurons with the longest axons. In humans, with motor axons up to a meter long, even a mild mutation in one copy of the gene that codes for kinesin-1, the primary anterograde axonal transport motor, can cause spastic paraplegia and other distal neuropathies.To address questions about the molecular mechanisms of organelle movement, we turned to Drosophila as a model system, because it offered rigorous genetic and molecular approaches to the identification and inhibition of specific elements of transport machinery. However, methods for direct observation of organelle transport were largely lacking. We describe here an approach that we developed for imaging the transport behaviors of specific organelles in the long motor axons of larvae. It is straightforward, the equipment is commonly available, and it provides a powerful tool for studying the contributions of specific proteins to organelle transport mechanisms.

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Source
http://dx.doi.org/10.1007/978-1-0716-1990-2_19DOI Listing

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