Literature DB >> 19109913

Role of glutamate autoreceptors at hippocampal mossy fiber synapses.

Hyung-Bae Kwon1, Pablo E Castillo.   

Abstract

Presynaptic autoreceptors modulate transmitter release at many synapses. At the mossy fiber to CA3 pyramidal cell (mf-CA3) synapse, two types of glutamatergic autoreceptors have been identified: transmitter release is reportedly suppressed by metabotropic glutamate receptors (mGluRs) and augmented by kainate receptors (KARs). However, the net effect of these autoreceptors when activated by endogenous glutamate is unknown. Here, we show that during low-frequency mossy fiber stimulation, glutamate acting through presynaptic mGluRs substantially suppresses transmitter release. However, using similar recording conditions, we find that presynaptic KARs are insufficient to facilitate transmitter release over a wide range of mossy fiber stimulus frequencies, indicating that the uniquely robust mf-CA3 short-term plasticity is KAR independent. Furthermore, we report that actions generally attributed to presynaptic KARs are likely due to activation of recurrent CA3 network activity. Thus, negative feedback via presynaptic mGluRs is the dominant mode of glutamatergic autoregulation at the mf-CA3 synapse.

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Year:  2008        PMID: 19109913      PMCID: PMC4454280          DOI: 10.1016/j.neuron.2008.10.045

Source DB:  PubMed          Journal:  Neuron        ISSN: 0896-6273            Impact factor:   17.173


  62 in total

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Journal:  J Physiol       Date:  2000-03-15       Impact factor: 5.182

Review 2.  The multifarious hippocampal mossy fiber pathway: a review.

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Review 10.  Kainate receptors and the induction of mossy fibre long-term potentiation.

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6.  Hippocampal Mossy Fibers Synapses in CA3 Pyramidal Cells Are Altered at an Early Stage in a Mouse Model of Alzheimer's Disease.

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8.  Interplay between synchronization of multivesicular release and recruitment of additional release sites support short-term facilitation at hippocampal mossy fiber to CA3 pyramidal cells synapses.

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9.  High-affinity kainate receptor subunits are necessary for ionotropic but not metabotropic signaling.

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10.  Long-term depression of synaptic kainate receptors reduces excitability by relieving inhibition of the slow afterhyperpolarization.

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