Abstract
In the mammalian retina, besides the conventional rod-cone system, a melanopsin-associated photoreceptive system exists that conveys photic information for accessory visual functions such as pupillary light reflex and circadian photo-entrainment. On ablation of the melanopsin gene, retinal ganglion cells that normally express melanopsin are no longer intrinsically photosensitive. Furthermore, pupil reflex, light-induced phase delays of the circadian clock and period lengthening of the circadian rhythm in constant light are all partially impaired. Here, we investigated whether additional photoreceptive systems participate in these responses. Using mice lacking rods and cones, we measured the action spectrum for phase-shifting the circadian rhythm of locomotor behaviour. This spectrum matches that for the pupillary light reflex in mice of the same genotype, and that for the intrinsic photosensitivity of the melanopsin-expressing retinal ganglion cells. We have also generated mice lacking melanopsin coupled with disabled rod and cone phototransduction mechanisms. These animals have an intact retina but fail to show any significant pupil reflex, to entrain to light/dark cycles, and to show any masking response to light. Thus, the rod-cone and melanopsin systems together seem to provide all of the photic input for these accessory visual functions.
MeSH Terms
Animals
Circadian Rhythm/physiology
Cyclic Nucleotide-Gated Cation Channels
Darkness
Female
Gene Deletion
Ion Channels/genetics,metabolism
Light
Male
Mice
Mice, Inbred C3H
Mice, Knockout
Motor Activity/physiology
Reflex, Pupillary/physiology
Retinal Cone Photoreceptor Cells/physiology
Retinal Ganglion Cells/metabolism
Retinal Rod Photoreceptor Cells/physiology
Rod Opsins/genetics,metabolism
Vision, Ocular/physiology
Visual Perception/physiology
Chemicals
Cyclic Nucleotide-Gated Cation Channels
Ion Channels
Rod Opsins
melanopsin
Authors & Affiliations
11 authors, click to expand affiliations / ORCID
Hattar S
Howard Hughes Medical Institute and Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA.
Lucas R J
Mrosovsky N
Thompson S
Douglas R H
Hankins M W
Lem J
Biel M
Hofmann F
Foster R G
Yau K-W
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