TY - JOUR
T1 - A Revised View on the Role of Surface AMPAR Mobility in Tuning Synaptic Transmission
T2 - Limitations, Tools, and Alternative Views
AU - Delgado, Jary Y.
AU - Selvin, Paul R.
N1 - Funding Information:
We would like to thank Meera Patel for editing assistance. Funding. This work was supported in part by NIH grants NS100019 and NS097610 and by NSF grant PHY-1430124 to PS and to NIH Grant NS103159 to JD.
Publisher Copyright:
© Copyright © 2018 Delgado and Selvin.
PY - 2018/7/20
Y1 - 2018/7/20
N2 - Calcium dynamics in presynaptic terminals regulate the response dynamics of most central excitatory synapses. However, this dogma has been challenged by the hypothesis that mobility of the postsynaptic alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid subtype glutamate receptors (AMPAR) plays a role in tuning fast excitatory synaptic transmission. In this review, we reevaluate the factors regulating postsynaptic AMPAR mobility, reassess the modeling parameters, analyze the experimental tools, and end by providing alternative ideas stemming from recent results. In particular, newer methods of labeling AMPARs with small fluorophores in live neurons, combined with super-resolution microscopy and sub-second dynamics, lends support to the idea that AMPARs are primarily within the synapse, are greatly constrained, and have much slower mobility than previously thought. We discuss new experiments which may be necessary to readdress the role of postsynaptic AMPAR mobility in tuning fast excitatory synaptic transmission.
AB - Calcium dynamics in presynaptic terminals regulate the response dynamics of most central excitatory synapses. However, this dogma has been challenged by the hypothesis that mobility of the postsynaptic alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid subtype glutamate receptors (AMPAR) plays a role in tuning fast excitatory synaptic transmission. In this review, we reevaluate the factors regulating postsynaptic AMPAR mobility, reassess the modeling parameters, analyze the experimental tools, and end by providing alternative ideas stemming from recent results. In particular, newer methods of labeling AMPARs with small fluorophores in live neurons, combined with super-resolution microscopy and sub-second dynamics, lends support to the idea that AMPARs are primarily within the synapse, are greatly constrained, and have much slower mobility than previously thought. We discuss new experiments which may be necessary to readdress the role of postsynaptic AMPAR mobility in tuning fast excitatory synaptic transmission.
KW - AMPAR
KW - desensitization
KW - diffusion
KW - high-resolution microscopy
KW - short-term plasticity
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U2 - 10.3389/fnsyn.2018.00021
DO - 10.3389/fnsyn.2018.00021
M3 - Review article
C2 - 30079019
SN - 1663-3563
VL - 10
JO - Frontiers in Synaptic Neuroscience
JF - Frontiers in Synaptic Neuroscience
M1 - 21
ER -