Photoreceptive Ganglion Cells Drive Circuits for Local Inhibition in the Mouse Retina

• Published in: The Journal of neuroscience 2021-02, Vol.41 (7), p.1489-1504
• Main Authors: Pottackal, Joseph, Walsh, Hannah L, Rahmani, Pouyan, Zhang, Kathy, Justice, Nicholas J, Demb, Jonathan B
• Format: Article
• Language: English
• Subjects: Amacrine cells; Amacrine Cells - physiology; Animals; Circuits; Corticotropin-releasing hormone; Corticotropin-Releasing Hormone - physiology; Electrical junctions; Electrophysiological Phenomena; Excitatory Postsynaptic Potentials - physiology; Feedback inhibition; Female; gamma-Aminobutyric Acid - physiology; Gap junctions; Gap Junctions - physiology; Inhibitory postsynaptic potentials; Interneurons; Male; Melanopsin; Mice; Mice, Inbred C57BL; Neural Inhibition - physiology; Neurons - physiology; Optogenetics; Photoreceptor Cells, Vertebrate - drug effects; Photoreceptor Cells, Vertebrate - physiology; Photosensitivity; Retina; Retina - physiology; Retinal Cone Photoreceptor Cells - drug effects; Retinal ganglion cells; Retinal Ganglion Cells - physiology; Retinal Rod Photoreceptor Cells - drug effects; Rod Opsins - metabolism; Synapses; Synapses - physiology; Visual pathways; γ-Aminobutyric acid
• ISSN: 0270-6474; 1529-2401; 1529-2401
• DOI: 10.1523/JNEUROSCI.0674-20.2020

Intrinsically photosensitive retinal ganglion cells (ipRGCs) exhibit melanopsin-dependent light responses that persist in the absence of rod and cone photoreceptor-mediated input. In addition to signaling anterogradely to the brain, ipRGCs signal retrogradely to intraretinal circuitry via gap junction-mediated electrical synapses with amacrine cells (ACs). However, the targets and functions of these intraretinal signals remain largely unknown. Here, in mice of both sexes, we identify circuitry that enables M5 ipRGCs to locally inhibit retinal neurons via electrical synapses with a nonspiking GABAergic AC. During pharmacological blockade of rod- and cone-mediated input, whole-cell recordings of corticotropin-releasing hormone-expressing (CRH ) ACs reveal persistent visual responses that require both melanopsin expression and gap junctions. In the developing retina, ipRGC-mediated input to CRH ACs is weak or absent before eye opening, indicating a primary role for this input in the mature retina (i.e., in parallel with rod- and cone-mediated input). Among several ipRGC types, only M5 ipRGCs exhibit consistent anatomical and physiological coupling to CRH ACs. Optogenetic stimulation of local CRH ACs directly drives IPSCs in M4 and M5, but not M1-M3, ipRGCs. CRH ACs also inhibit M2 ipRGC-coupled spiking ACs, demonstrating direct interaction between discrete networks of ipRGC-coupled interneurons. Together, these results demonstrate a functional role for electrical synapses in translating ipRGC activity into feedforward and feedback inhibition of local retinal circuits. Melanopsin directly generates light responses in intrinsically photosensitive retinal ganglion cells (ipRGCs). Through gap junction-mediated electrical synapses with retinal interneurons, these uniquely photoreceptive RGCs may also influence the activity and output of neuronal circuits within the retina. Here, we identified and studied an electrical synaptic circuit that, in principle, could couple ipRGC activity to the chemical output of an identified retinal interneuron. Specifically, we found that M5 ipRGCs form electrical synapses with corticotropin-releasing hormone-expressing amacrine cells, which locally release GABA to inhibit specific RGC types. Thus, ipRGCs are poised to influence the output of diverse retinal circuits via electrical synapses with interneurons.