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Updated: May 6, 2026

An Optical Assay for Synaptic Vesicle Recycling in Cultured Neurons Overexpressing Presynaptic Proteins
Published on: June 26, 2018
Adaptive and non-adaptive changes in activity-deprived presynaptic terminals.
Süzel Horellou1, Olivier Pascual, Antoine Triller
1Institute of Biology of the Ecole Normale Supérieure, 46 rue d'Ulm, 75005, Paris, France; INSERM U1024, Paris, France; CNRS UMR8197, Paris, France.
Synaptic vesicle docking increases after activity blockade, but not due to terminal size or Rab3-interacting molecule 1/2 (RIM1/2) levels. RIM1/2 distribution changes, not amount, may explain altered synaptic function.
Area of Science:
- Neuroscience
- Cell Biology
- Synaptic Plasticity
Background:
- Regulation of docked vesicles at the synapse is not fully understood.
- Chronic activity blockade increases docked vesicle numbers, offering a model for study.
Purpose of the Study:
- To investigate if docked vesicle number is regulated by presynaptic terminal size or Rab3-interacting molecule 1/2 (RIM1/2) levels.
- To explore the role of RIM1/2 in synaptic homeostasis.
Main Methods:
- Mouse hippocampal slice cultures were treated with tetrodotoxin to block activity.
- High-pressure freezing and electron microscopy were used for analysis.
- Immunocytochemistry assessed RIM1/2 levels and distribution.
Main Results:
- Activity blockade increased docked vesicles, active zone size, and GluA2 amount, but not total vesicles or presynaptic area.
- RIM1/2 levels per terminal remained unchanged, but its distribution was altered.
- Miniature excitatory postsynaptic current frequency and amplitude were unaffected, but amplitude distribution changed.
Conclusions:
- Synaptic junctions exhibit specific homeostatic regulation.
- Docked vesicle numbers are not regulated by the total amount of RIM1/2.
- Altered RIM1/2 distribution, not quantity, may reconcile morphological and electrophysiological findings.
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