Plasticity of neurotransmitter release sites in temporal coding, homeostasis, learning and disease

This project aims to explore the mechanisms of synaptic release site plasticity in Drosophila to understand its role in neural function, behavior, and disease treatment.

Subsidie
€ 2.000.000
2024

Projectdetails

Introduction

Virtually all neural computation relies on synaptic plasticity, the dynamic change of chemical synaptic communication achieved by transmitter exocytosis from vesicles at presynaptic release sites to activate postsynaptic receptors. Plasticity mechanisms must be powerful, scalable, and sustainable over all timescales of neural processing.

Research Focus

Which part of the synaptic machinery is the best-suited plasticity target? The number of synaptic vesicles greatly outnumbers that of release sites, essentially making the sites gatekeepers of all neural communication. Release site plasticity could thus be pivotal to all neural processing.

Recent Discoveries

We recently discovered the molecular identity of release sites (conserved Unc13 proteins) and found evidence of potent release site plasticity on timescales of milliseconds, minutes, and days. We are now in the position to use this molecular handle to unravel the principles of this plasticity, which will be key to understanding neural function, behavior, and disease.

Methodology

Owing to the conserved process and machinery, we will harness the power of Drosophila genetics to elucidate general mechanisms and broad relevance of three distinct release-site plasticity phenomena:

  1. Release site switching for millisecond facilitation of transmission and its contribution to network pattern generation as needed for locomotion.
  2. Release site activation for minutes’ potentiation of transmitter release and its role in homeostasis and learning.
  3. Release site accumulation for long-lasting potentiation with regained dynamic range and its role in homeostasis and memory.

Disease Implications

Finally, disease mutations accumulate in proteins relating to release site function. We will thus:

  1. Investigate whether these mutations affect release site plasticity in flies and attempt treatment of their induced defects by artificial enhancement of plasticity.

Conclusion

My work will set the stage to establish the investigation of the role of this novel and fundamental plasticity in neural function and disease.

Financiële details & Tijdlijn

Financiële details

Subsidiebedrag€ 2.000.000
Totale projectbegroting€ 2.000.000

Tijdlijn

Startdatum1-1-2024
Einddatum31-12-2028
Subsidiejaar2024

Partners & Locaties

Projectpartners

  • KOBENHAVNS UNIVERSITETpenvoerder

Land(en)

Denmark

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