A Quantitative Model of Sporadic Axonal Degeneration in the Drosophila Visual System

In human neurodegenerative diseases, neurons undergo axonal degeneration months to years before they die. Here, we developed a system modeling early degenerative events in Drosophila adult photoreceptor cells. Thanks to the stereotypy of their axonal projections, this system delivers quantitative data on sporadic and progressive axonal degeneration of photoreceptor cells. Using this method, we show that exposure of adult female flies to a constant light stimulation for several days overcomes the intrinsic resilience of R7 photoreceptors and leads to progressive axonal degeneration. This was not associated with apoptosis. We furthermore provide evidence that loss of synaptic integrity between R7 and a postsynaptic partner preceded axonal degeneration, thus recapitulating features of human neurodegenerative diseases. Finally, our experiments uncovered a role of postsynaptic partners of R7 to initiate degeneration, suggesting that postsynaptic cells signal back to the photoreceptor to maintain axonal structure. This model can be used to dissect cellular and circuit mechanisms involved in the early events of axonal degeneration, allowing for a better understanding of how neurons cope with stress and lose their resilience capacities.

Automated summary

This study develops a system to model early degeneration events in Drosophila adult photoreceptor cells. Exposure of adult female flies to constant light stimulation leads to progressive axonal degeneration, independent of apoptosis. Loss of synaptic integrity between photoreceptor cells precedes axonal degeneration, resembling features of human neurodegenerative diseases. This study also uncovers the role of postsynaptic partners in initiating degeneration and suggests that postsynaptic cells signal back to maintain axonal structure.