Extrasynaptic NMDA Receptors on Rod Pathway Amacrine Cells: Molecular Composition, Activation, and Signaling

• Published in: The Journal of neuroscience 2019-01, Vol.39 (4), p.627-650
• Main Authors: Veruki, Margaret L, Zhou, Yifan, Castilho, Áurea, Morgans, Catherine W, Hartveit, Espen
• Format: Article
• Language: English
• Subjects: Activation; Amacrine cells; Amacrine Cells - drug effects; Amacrine Cells - metabolism; Amacrine Cells - ultrastructure; Animals; Bipolar cells; Calcium (intracellular); Calcium - metabolism; Calcium imaging; Calcium ions; Composition; Connexin 36; Connexins - metabolism; Coupling (molecular); Data processing; Dendrites; Dendrites - metabolism; Excitatory Postsynaptic Potentials - drug effects; Female; gamma-Aminobutyric Acid - physiology; Gap Junction delta-2 Protein; Gap Junctions - drug effects; Glutamatergic transmission; Glutamic acid receptors (ionotropic); In Vitro Techniques; Localization; N-Methyl-D-aspartic acid receptors; Patch-Clamp Techniques; Pharmacology; Presynapse; Rats; Rats, Wistar; Receptor mechanisms; Receptors; Receptors, N-Methyl-D-Aspartate - drug effects; Receptors, N-Methyl-D-Aspartate - metabolism; Recording; Retina; Retinal Bipolar Cells - drug effects; Retinal Bipolar Cells - metabolism; Retinal cells; Retinal Rod Photoreceptor Cells - metabolism; Retinal Rod Photoreceptor Cells - ultrastructure; Rodents; Signal processing; Signal Transduction - drug effects
• ISSN: 0270-6474; 1529-2401
• DOI: 10.1523/JNEUROSCI.2267-18.2018

In the rod pathway of the mammalian retina, axon terminals of glutamatergic rod bipolar cells are presynaptic to AII and A17 amacrine cells in the inner plexiform layer. Recent evidence suggests that both amacrines express NMDA receptors, raising questions concerning molecular composition, localization, activation, and function of these receptors. Using dual patch-clamp recording from synaptically connected rod bipolar and AII or A17 amacrine cells in retinal slices from female rats, we found no evidence that NMDA receptors contribute to postsynaptic currents evoked in either amacrine. Instead, NMDA receptors on both amacrine cells were activated by ambient glutamate, and blocking glutamate uptake increased their level of activation. NMDA receptor activation also increased the frequency of GABAergic postsynaptic currents in rod bipolar cells, suggesting that NMDA receptors can drive release of GABA from A17 amacrines. A striking dichotomy was revealed by pharmacological and immunolabeling experiments, which found GluN2B-containing NMDA receptors on AII amacrines and GluN2A-containing NMDA receptors on A17 amacrines. Immunolabeling also revealed a clustered organization of NMDA receptors on both amacrines and a close spatial association between GluN2B subunits and connexin 36 on AII amacrines, suggesting that NMDA receptor modulation of gap junction coupling between these cells involves the GluN2B subunit. Using multiphoton Ca imaging, we verified that activation of NMDA receptors evoked an increase of intracellular Ca in dendrites of both amacrines. Our results suggest that AII and A17 amacrines express clustered, extrasynaptic NMDA receptors, with different and complementary subunits that are likely to contribute differentially to signal processing and plasticity. Glutamate is the most important excitatory neurotransmitter in the CNS, but not all glutamate receptors transmit fast excitatory signals at synapses. NMDA-type glutamate receptors act as voltage- and ligand-gated ion channels, with functional properties determined by their specific subunit composition. These receptors can be found at both synaptic and extrasynaptic sites on neurons, but the role of extrasynaptic NMDA receptors is unclear. Here, we demonstrate that retinal AII and A17 amacrine cells, postsynaptic partners at rod bipolar dyad synapses, express extrasynaptic (but not synaptic) NMDA receptors, with different and complementary GluN2 subunits. The localization of GluN2A-containing rec