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.
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:
- Release site switching for millisecond facilitation of transmission and its contribution to network pattern generation as needed for locomotion.
- Release site activation for minutes’ potentiation of transmitter release and its role in homeostasis and learning.
- 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:
- 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
Startdatum | 1-1-2024 |
Einddatum | 31-12-2028 |
Subsidiejaar | 2024 |
Partners & Locaties
Projectpartners
- KOBENHAVNS UNIVERSITETpenvoerder
Land(en)
Vergelijkbare projecten binnen European Research Council
Project | Regeling | Bedrag | Jaar | Actie |
---|---|---|---|---|
Cracking the Synaptic Memory CodeThis project aims to uncover how local protein production at synapses contributes to memory encoding in the brain using advanced imaging and sequencing techniques. | ERC Starting... | € 1.500.000 | 2023 | Details |
Revealing the Landscape of Synaptic Diversity by Cell type- and Synapse-specific Proteomics and TranscriptomicsThis project aims to elucidate the molecular diversity of synapses by analyzing their proteomes and transcriptomes across different brain areas, using advanced sorting and profiling techniques. | ERC Advanced... | € 2.498.575 | 2022 | Details |
The synaptic active zone as a signaling hub for sleep homeostasis and resilienceThe SynProtect project aims to investigate the role of presynaptic active zone plasticity (PreScale) in enhancing brain resilience to sleep deprivation through genetic manipulation and advanced imaging techniques. | ERC Advanced... | € 2.242.580 | 2023 | Details |
Lysosomal exocytosis of metastable proteins to control synaptic functionThe LEXSYN project aims to investigate lysosomal exocytosis in dendrites to understand its role in synaptic plasticity and neurodegeneration, utilizing advanced imaging and new monitoring tools. | ERC Starting... | € 2.037.356 | 2025 | Details |
Unravelling the Physiological Roles of GPCR Voltage DependenceThis project aims to investigate the physiological roles of GPCR voltage dependence in Drosophila using electrophysiology and imaging to understand its impact on neuronal activity and behavior. | ERC Consolid... | € 1.992.500 | 2023 | Details |
Cracking the Synaptic Memory Code
This project aims to uncover how local protein production at synapses contributes to memory encoding in the brain using advanced imaging and sequencing techniques.
Revealing the Landscape of Synaptic Diversity by Cell type- and Synapse-specific Proteomics and Transcriptomics
This project aims to elucidate the molecular diversity of synapses by analyzing their proteomes and transcriptomes across different brain areas, using advanced sorting and profiling techniques.
The synaptic active zone as a signaling hub for sleep homeostasis and resilience
The SynProtect project aims to investigate the role of presynaptic active zone plasticity (PreScale) in enhancing brain resilience to sleep deprivation through genetic manipulation and advanced imaging techniques.
Lysosomal exocytosis of metastable proteins to control synaptic function
The LEXSYN project aims to investigate lysosomal exocytosis in dendrites to understand its role in synaptic plasticity and neurodegeneration, utilizing advanced imaging and new monitoring tools.
Unravelling the Physiological Roles of GPCR Voltage Dependence
This project aims to investigate the physiological roles of GPCR voltage dependence in Drosophila using electrophysiology and imaging to understand its impact on neuronal activity and behavior.