Abstract
The mossy fiber to CA3 pyramidal neuron synapse in the hippocampus displays an atypical form of NMDA receptor-independent long-term potentiation (LTP). Plasticity at this synapse is expressed in the presynaptic terminal as an elevated probability of neurotransmitter release. However, evidence indicates that postsynaptic mechanisms and trans-synaptic signaling through an association between postsynaptic EphB receptors and presynaptic B-ephrins are necessary for the induction of LTP. Here we show that ephrin-B3 protein is highly expressed in mossy fiber axons and terminals. There are specific deficits in mossy fiber LTP in mice in which the cytoplasmic C-terminal signaling domain of the ephrin-B3 protein is replaced with β-galactosidase. These deficits are not observed in ephrin-B3 null mutant mice because of functional redundancy by virtue of other B-ephrins. These results indicate that B-ephrin reverse signaling into the presynaptic mossy fiber bouton is required for the induction of NMDA receptor-independent LTP at this synapse.
Original language | English (US) |
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Pages (from-to) | 3474-3481 |
Number of pages | 8 |
Journal | Journal of Neuroscience |
Volume | 26 |
Issue number | 13 |
DOIs | |
State | Published - Mar 29 2006 |
Keywords
- Ephrin
- Hippocampus
- Long-term potentiation
- Mossy fiber
- Presynaptic signaling
- Pyramidal neuron
ASJC Scopus subject areas
- General Neuroscience