Synaptic inputs to retinal ganglion cells that set the circadian clock

• Published in: The European journal of neuroscience 2006-08, Vol.24 (4), p.1117-1123
• Main Authors: Perez-Leon, Jorge Alberto, Warren, Erin J., Allen, Charles N., Robinson, David W., Lane Brown, R
• Format: Article
• Language: English
• Subjects: Animals; Bicuculline - metabolism; Biological Clocks - physiology; Circadian Rhythm - physiology; circadian rhythms; Excitatory Amino Acid Antagonists - metabolism; GABA Antagonists - metabolism; Glycine Agents - metabolism; intrinsic light response; Kynurenic Acid - metabolism; Light; melanopsin; Neural Pathways - metabolism; Neural Pathways - physiology; Patch-Clamp Techniques; photoentrainment; photoreceptor; postsynaptic current; Quinoxalines - metabolism; Rats; Rats, Sprague-Dawley; Receptors, GABA - metabolism; Receptors, Glutamate - metabolism; Retinal Ganglion Cells - cytology; Retinal Ganglion Cells - metabolism; Rod Opsins - metabolism; Strychnine - metabolism; Synapses - metabolism; Synaptic Transmission - physiology; Tetrodotoxin - metabolism
• ISSN: 0953-816X; 1460-9568
• DOI: 10.1111/j.1460-9568.2006.04999.x

Melanopsin‐containing retinal ganglion cells (RGCs) project to the suprachiasmatic nuclei (SCN) and mediate photoentrainment of the circadian system. Melanopsin is a novel retinal‐based photopigment that renders these cells intrinsically photosensitive (ip). Although genetic ablation of melanopsin abolishes the intrinsic light response, it has a surprisingly minor effect on circadian photoentrainment. This and other non‐visual responses to light are lost only when the melanopsin deficiency is coupled with mutations that disable classical rod and cone photoreceptors, suggesting that melanopsin‐containing RGCs also receive rod‐ and cone‐driven synaptic inputs. Using whole‐cell patch‐clamp recording, we demonstrate that light triggers synaptic currents in ipRGCs via activation of ionotropic glutamate and γ‐aminobutyric acid (GABA) receptors. Miniature postsynaptic currents (mPSCs) were clearly observed in ipRGCs, although they were less robust and were seen less frequently than those seen in non‐ip cells. Pharmacological treatments revealed that the majority of ipRGCs receive excitatory glutamatergic inputs that were blocked by DNQX and/or kynurenic acid, as well as inhibitory GABAergic inputs that were blocked by bicuculline. Other ipRGCs received either glutamatergic or GABAergic inputs nearly exclusively. Although strychnine (Strych)‐sensitive mPSCs were evident on many non‐ipRGCs, indicating the presence of glycinergic inputs, we saw no evidence of Strych‐sensitive events in ipRGCs. Based on these results, it is clear that SCN‐projecting RGCs can respond to light both via an intrinsic melanopsin‐based signaling cascade and via a synaptic pathway driven by classical rod and/or cone photoreceptors. It remains to be determined how the ipRGCs integrate these temporally distinct inputs to generate the signals that mediate circadian photoentrainment and other non‐visual responses to light.