TY - JOUR
T1 - Coincident activation of metabotropic glutamate receptors and NMDA receptors (NMDARs) downregulates perisynaptic/extrasynaptic NMDARs and enhances high-fidelity neurotransmission at the developing calyx of Held synapse
AU - Joshi, Indu
AU - Yang, Yi Mei
AU - Wang, Lu Yang
PY - 2007/9/12
Y1 - 2007/9/12
N2 - NMDA receptors (NMDARs) are usually downregulated in developing central synapses, but underlying mechanisms and functional consequences are not well established. Using developing calyx of Held synapses in the mouse auditory brainstem, we show here that pairing presynaptic stimulation with postsynaptic depolarization results in a persistent downregulation in the summated amplitude of NMDAR-mediated EPSCs (NMDAR-EPSCs) during a train of stimuli (100/200 Hz, 100 ms) at both 22°C and 35°C. In contrast, the amplitude of single NMDAR-EPSCs or AMPA receptor-mediated EPSCs in the same synapses is not significantly altered, implying a preferential downregulation of perisynaptic/extrasynaptic NMDARs. Induction of this downregulation is blocked by antagonists for NMDARs or group I metabotropic glutamate receptors (mGluRs), suggesting that coincident activation of these two receptors is required. When the postsynaptic neuron is loaded with the fast Ca2+ buffer BAPTA or depolarized to +60 mV to reduce the driving force for Ca2+ influx, downregulation of the summated NMDAR-EPSCs is abolished, indicating Ca 2+ plays a critical role in the induction. The expression of this downregulation depends on ongoing synaptic activity, and is attenuated by a dynamin peptide (D15) that blocks clathrin-dependent internalization. We further demonstrated that the same induction paradigm specifically reduces NMDAR-dependent plateau potential and aberrant spike firings during repetitive activity. Together, our results suggest that coincident activation of mGluRs and NMDARs during intense synaptic activity may lead to selective endocytosis of NMDARs in the perisynaptic/extrasynaptic domain, and implicate that mGluRs are potentially important for gating development of high-fidelity neurotransmission at this synapse.
AB - NMDA receptors (NMDARs) are usually downregulated in developing central synapses, but underlying mechanisms and functional consequences are not well established. Using developing calyx of Held synapses in the mouse auditory brainstem, we show here that pairing presynaptic stimulation with postsynaptic depolarization results in a persistent downregulation in the summated amplitude of NMDAR-mediated EPSCs (NMDAR-EPSCs) during a train of stimuli (100/200 Hz, 100 ms) at both 22°C and 35°C. In contrast, the amplitude of single NMDAR-EPSCs or AMPA receptor-mediated EPSCs in the same synapses is not significantly altered, implying a preferential downregulation of perisynaptic/extrasynaptic NMDARs. Induction of this downregulation is blocked by antagonists for NMDARs or group I metabotropic glutamate receptors (mGluRs), suggesting that coincident activation of these two receptors is required. When the postsynaptic neuron is loaded with the fast Ca2+ buffer BAPTA or depolarized to +60 mV to reduce the driving force for Ca2+ influx, downregulation of the summated NMDAR-EPSCs is abolished, indicating Ca 2+ plays a critical role in the induction. The expression of this downregulation depends on ongoing synaptic activity, and is attenuated by a dynamin peptide (D15) that blocks clathrin-dependent internalization. We further demonstrated that the same induction paradigm specifically reduces NMDAR-dependent plateau potential and aberrant spike firings during repetitive activity. Together, our results suggest that coincident activation of mGluRs and NMDARs during intense synaptic activity may lead to selective endocytosis of NMDARs in the perisynaptic/extrasynaptic domain, and implicate that mGluRs are potentially important for gating development of high-fidelity neurotransmission at this synapse.
KW - AMPA receptors
KW - Calyx of Held-MNTB synapse
KW - Developmental plasticity
KW - NMDA receptors
KW - Neurotransmission
KW - Spike firing
KW - mGluRs
UR - http://www.scopus.com/inward/record.url?scp=34548615390&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=34548615390&partnerID=8YFLogxK
U2 - 10.1523/JNEUROSCI.2506-07.2007
DO - 10.1523/JNEUROSCI.2506-07.2007
M3 - Article
C2 - 17855613
AN - SCOPUS:34548615390
SN - 0270-6474
VL - 27
SP - 9989
EP - 9999
JO - Journal of Neuroscience
JF - Journal of Neuroscience
IS - 37
ER -