Our recent studies have examined circadian photoreception in mice with
hereditary retinal disorders (rd/rd and rds/rds). Despite the loss of
visual function in these mice, circadian responses to light remain un
affected. Using c-fos expression within the suprachiasmatic nuclei (SC
N) as a marker of neural activation of the circadian entrainment pathw
ay, we have found identical levels of Fos in the SCN of rd/rd and +/mice in response to retinal illumination. On the basis of action spect
rum studies, and measurements of photopigment retinoids using high-pre
ssure liquid chromatography, we believe that the photopigment mediatin
g circadian responses to light is based upon an opsin, and that 11-cis
-retinaldehyde is the photopigment chromophore. Preliminary measuremen
ts of mouse rod opsin, blue cone, and green-red cone opsin messenger R
NA in retinally degenerate mice suggest that none of these opsins is e
xclusively used to mediate circadian responses to light. Collectively,
our data suggest that circadian photoreception can be maintained by a
very small number of rod or cone cells without outer segments, or, al
ternatively, is performed by an unrecognized class of photoreceptive c
ell within the mammalian retina.