B-ephrin reverse signaling is required for NMDA-independent long-term potentiation of mossy fibers in the hippocampus

被引:82
作者
Armstrong, JN
Saganich, MJ
Xu, NJ
Henkemeyer, M
Heinemann, SF
Contractor, A
机构
[1] Northwestern Univ, Feinberg Sch Med, Dept Physiol, Chicago, IL 60611 USA
[2] Northwestern Univ, Feinberg Sch Med, Inst Neurosci, Chicago, IL 60611 USA
[3] Salk Inst Biol Studies, Mol Neurobiol Lab, La Jolla, CA 93037 USA
[4] Univ Texas, SW Med Ctr, Ctr Dev Biol, Dallas, TX 75235 USA
[5] Univ Texas, SW Med Ctr, Kent Waldrep Fdn, Ctr Basic Neurosci Res Nerve Growth & Regenerat, Dallas, TX 75235 USA
[6] Northwestern Univ, Feinberg Sch Med, Dept Physiol, Chicago, IL 60611 USA
[7] Northwestern Univ, Feinberg Sch Med, Inst Neurosci, Chicago, IL 60611 USA
关键词
long-term potentiation; mossy fiber; hippocampus; ephrin; pyramidal neuron; presynaptic signaling;
D O I
10.1523/JNEUROSCI.4338-05.2006
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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 beta-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.
引用
收藏
页码:3474 / 3481
页数:8
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