Oxytocin-driven territorial mapping in the mammalian hippocampal formation
This project aims to investigate how the oxytocin system influences spatial and territorial representations in the entorhinal-hippocampal network across five mammalian species.
Projectdetails
Introduction
Orienting in space recruits brain mechanisms well conserved across mammalian species. Within the entorhinal-hippocampal network, a core system of spatially-selective cells supports spatial geometry computations. Yet, when navigating familiar surroundings, neural computations of space usually escape our attention.
Social Territories
Instead, we parse space into socially meaningful territories. Territorial boundaries are social in nature since they capture the location of utilities available to individuals tied to group hierarchy and affiliation.
Research Question
How does our brain integrate geometry and territory? We propose that this process is regulated by the oxytocin (OT) system, acting on the entorhinal-hippocampal regions. OT, a hypothalamic neuropeptide known for its pro-social effects in mammals, modulates neural activity in the hippocampal formation, but its potential role in territorial representations has not yet been studied.
Methodology
Here, experts in complementary fields – social behaviors, spatial navigation, neurophysiology, anatomy, and cell signaling – will study brain similarities and differences of socio-territorial strategies in five mammalian species:
- Bats
- Mice
- Rats
- Marmosets
- Macaques
Central Goal
Our central goal is to investigate how neurons coding for space (e.g., place cells, boundary cells, grid cells) respond to perceived socio-spatial parameters of ownership, utility, and social hierarchies.
Expectations
We expect spatial cells to be sensitive to territorial manipulations (ownership, proximity, intrusion), regulated by OT in a context-dependent manner.
Potential Outcomes
- OT inhibition may enhance territorial defense when territories are challenged (e.g., conspecific approaches or transgresses borders) and may sharpen territorial boundary representations.
- Conversely, OT stimulation could blur the boundaries of territorial perception.
Conclusion
Our cross-species perspective will be the first to provide information on possible species-specific vs. shared neural mechanisms for territorial maps and OT-induced hippocampal plasticity.
Financiële details & Tijdlijn
Financiële details
Subsidiebedrag | € 10.000.000 |
Totale projectbegroting | € 10.000.000 |
Tijdlijn
Startdatum | 1-6-2023 |
Einddatum | 31-5-2029 |
Subsidiejaar | 2023 |
Partners & Locaties
Projectpartners
- ZENTRALINSTITUT FUER SEELISCHE GESUNDHEITpenvoerder
- CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE CNRS
- TECHNION - ISRAEL INSTITUTE OF TECHNOLOGY
- THE HEBREW UNIVERSITY OF JERUSALEM
- WEIZMANN INSTITUTE OF SCIENCE
- UNIVERSITY OF HAIFA
Land(en)
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The neural basis of dynamic territorial aggression and fear
This project investigates the neural mechanisms of territorial behavior in mice, focusing on a hypothalamic switch between aggression and avoidance to enhance understanding of aggression and fear in humans.
Oxytocin regulates marmosets’ affiliation and vocal communication
This project investigates how oxytocin influences vocal communication in marmoset monkeys by analyzing neural mechanisms in social contexts, aiming to enhance understanding of primate social behavior.
Neural Circuits Enabling Navigational Simulations
This project aims to uncover the neural mechanisms of goal-directed navigation in rats by studying the interactions between the orbitofrontal cortex and hippocampus, enhancing understanding of spatial reasoning and psychiatric disorders.
Task-relevant cognitive maps and their role in spatial decision-making
This project aims to uncover how the brain forms internal cognitive maps and makes spatial decisions by studying rats' neural activity and decision-making processes through advanced techniques.
Neuronal implementation of cognitive maps for navigation
This project aims to elucidate the mechanisms of cognitive maps in zebrafish by integrating brain imaging, electron microscopy, and transcriptomics to understand neuronal connectivity and behavior.