Abstract
Experiments were conducted in both HEK cells and cerebellar neurons to investigate whether CXC chemokine receptor 2 (CXCR2) is functionally coupled to GluR1. The co-expression of CXCR2 with GluR1 in HEK cells increased (i) the GluR1 "apparent" affinity for the transmitter; (ii) the GluR1 channel open probability; and (iii) GluR1 binding site cooperativity upon CXCR2 stimulation with CXC chemokine ligand 2 (CXCL2). The affinity of C-terminal-deleted GluR1 for glutamate (Glu) remained stable instead. Furthermore, CXCL2 increased the binding site cooperativity of AMPA receptors in rat cerebellar granule cells; and the amplitude of spontaneous excitatory postsynaptic current (sEPSCs) in Purkinje neurons (PNs). Our findings indicate that the coupling of CXCR2 with GluR1 may modulate glutamatergic synaptic transmission.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Binding Sites / drug effects
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Binding Sites / immunology
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Cells, Cultured
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Central Nervous System / immunology
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Central Nervous System / metabolism*
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Cerebellar Cortex / drug effects
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Cerebellar Cortex / immunology
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Cerebellar Cortex / metabolism
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Chemokines, CXC / immunology
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Chemokines, CXC / metabolism*
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Chemokines, CXC / pharmacology
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DNA, Complementary / genetics
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Dose-Response Relationship, Drug
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Excitatory Amino Acid Antagonists / pharmacology
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Excitatory Postsynaptic Potentials / drug effects
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Excitatory Postsynaptic Potentials / immunology
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Gene Expression Regulation / drug effects
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Gene Expression Regulation / immunology
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Glutamic Acid / metabolism*
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Glutamic Acid / pharmacology
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Humans
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Ion Channels / genetics
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Ion Channels / immunology
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Neurons / drug effects
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Neurons / immunology
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Neurons / metabolism
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Rats
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Rats, Sprague-Dawley
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Rats, Wistar
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Receptors, AMPA / genetics
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Receptors, AMPA / immunology
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Receptors, AMPA / metabolism*
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Receptors, Interleukin-8B / genetics
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Receptors, Interleukin-8B / immunology
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Receptors, Interleukin-8B / metabolism*
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Synapses / immunology
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Synapses / metabolism*
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Synaptic Transmission / immunology*
Substances
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Chemokines, CXC
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DNA, Complementary
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Excitatory Amino Acid Antagonists
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Ion Channels
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Receptors, AMPA
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Receptors, Interleukin-8B
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Glutamic Acid
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glutamate receptor ionotropic, AMPA 1