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DOI: 10.3791/57557-v
This article presents a Drosophila sensory neuron injury model that integrates in vivo live imaging and two-photon laser axotomy/dendriotomy. This approach leverages the fly genetic toolbox to screen for potential neuroregeneration promoters and inhibitors.
Here, we present a protocol using the Drosophila sensory neuron - dendritic arborization (da) neuron injury model, which combines in vivo live imaging, two-photon laser axotomy/dendriotomy, and the powerful fly genetic toolbox, as a platform for screening potential promoters and inhibitors of neuroregeneration.
The overall goal of this Drosophila larval sensory neuron injury model is to combine in vivo live imaging, two-photon laser axotomy/dendriotomy, and the powerful fly genetic toolbox into a platform for screening potential promoters and inhibitors of neuroregeneration. This method will help address key questions in a field of neurogeneration, such as by identifying new intrinsic and extrinsic regulator for neurogeneration, both in a peripheral and central nerve system. The main advantage of this technique is that novel candidates for neuroregeneration can be screened in an easy, fast and cheap way.
Though this system can provide insight into neuroregeneration, it can also be applied to other systems, such as neurodegenerative diseases and neuron-glia interactions. Generally, individuals new to this method will struggle because different experimental setups that utilize different types of neurons are used to model axon versus dendritic regeneration. For the larvae collection, prepare culture bottles as follows.
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