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Calcium Imaging Reveals a Network of Intrinsically Light-Sensitive Inner-Retinal Neurons

Background: Mice lacking rod and cone photoreceptors (rd/rd cl) are still able to regulate a range of responses to light, including circadian photoentrainment, the pupillary light reflex, and suppression of pineal melatonin by light. These data are consistent with the presence of a novel inner-retin...

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Bibliographic Details
Published in:Current biology 2003-08, Vol.13 (15), p.1290-1298
Main Authors: Sekaran, Sumathi, Foster, Russell G., Lucas, Robert J., Hankins, Mark W.
Format: Article
Language:English
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Summary:Background: Mice lacking rod and cone photoreceptors (rd/rd cl) are still able to regulate a range of responses to light, including circadian photoentrainment, the pupillary light reflex, and suppression of pineal melatonin by light. These data are consistent with the presence of a novel inner-retinal photoreceptor mediating non-image-forming irradiance detection. Results: We have examined the nature and extent of intrinsic light sensitivity in rd/rd cl retinae by monitoring the effect of light stimulation (470 nm) on intracellular Ca2+ via FURA-2 imaging. Using this approach, which does not rely on pharmacological or surgical isolation of ganglion cells from the rod and cone photoreceptors, we identified a population of light-sensitive neurons in the ganglion cell layer (GCL). Retinal illumination induced an increase of intracellular Ca2+ in ∼2.7% of the neurons. The light-evoked Ca2+ fluxes were dependent on the intensity and duration of the light stimulus. The light-responsive units formed an extensive network that could be uncoupled by application of the gap junction blocker carbenoxolone. Three types of light-evoked Ca2+ influx were observed: sustained, transient, and repetitive, which are suggestive of distinct functional classes of GCL photoreceptors. Conclusions: Collectively, our data reveal a heterogeneous syncytium of intrinsically photosensitive neurons in the GCL coupled to a secondary population of light-driven cells, in the absence of rod and cone inputs.
ISSN:0960-9822
1879-0445
DOI:10.1016/S0960-9822(03)00510-4