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Regulation of the extracellular matrix by dopamine during adult learning

Subject Area Molecular Biology and Physiology of Neurons and Glial Cells
Cognitive, Systems and Behavioural Neurobiology
Term from 2020 to 2024
Project identifier Deutsche Forschungsgemeinschaft (DFG) - Project number 441274012
 
Final Report Year 2025

Final Report Abstract

A specialized form of the extracellular matrix (ECM) emerges during adolescence, stabilizing synaptic networks but limiting plasticity in the adult brain. This project investigated how dynamic ECM regulation—specifically of the proteoglycan brevican— enables plasticity during adult learning, and whether this process depends on neuromodulators like dopamine. Using acute hippocampal slices, we showed that the proteases ADAMTS-4 and -5 mediate activity-dependent cleavage of brevican shortly after synaptic stimulation. Blocking these proteases impaired the formation of new dendritic protrusions, highlighting ECM breakdown as a prerequisite for structural synaptic plasticity. To extend these insights to intact networks, we used in vivo laminar recordings in gerbils combined with ECM degradation. We found a redistribution of synaptic activity from deep to superficial layers and increased lateral integration, suggesting that ECM integrity shapes cortical input processing. Building on this, we developed a new model combining chronic laminar recordings with a reversal learning task. We found that prediction errors activated deep cortical layers—mirroring dopaminergic error signaling—while successful learning shifted activity to superficial layers with increased gamma and beta oscillations. Together, these findings establish that ECM remodeling enables adaptive cortical reorganization during learning. The project thus links molecular ECM plasticity with systems-level circuit dynamics during behavior.

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