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Circadian control of photoreceptor outer segment membrane turnover in mice genetically incapable of melatonin synthesis

Published online by Cambridge University Press:  01 September 1999

MICHAEL S. GRACE
Affiliation:
National Science Foundation Science and Technology Center for Biological Timing, and Department of Biology, Gilmer Hall, University of Virginia, Charlottesville
ATSUHIKO CHIBA
Affiliation:
National Science Foundation Science and Technology Center for Biological Timing, and Department of Biology, Gilmer Hall, University of Virginia, Charlottesville Permanent address: Life Science Institute, Sophia University, Tokyo, Japan.
MICHAEL MENAKER
Affiliation:
National Science Foundation Science and Technology Center for Biological Timing, and Department of Biology, Gilmer Hall, University of Virginia, Charlottesville

Abstract

Vertebrate retinal photoreceptors periodically shed membrane from their outer segment distal tips; this material is phagocytosed and degraded by the retinal pigmented epithelium. Both a circadian oscillator and the daily light–dark cycle affect disk shedding, and the effects of both may be mediated by melatonin. To clarify melatonin's role in this process, we asked whether endogenous melatonin is required for rhythmic disk shedding in mouse retina. We analyzed disk shedding in two mouse strains: C3H, which produce melatonin in retina and pineal under the control of circadian oscillators, and C57BL/6, which do not produce melatonin. In cyclic light, both strains exhibited a robust cycle of disk phagosome content in the pigmented epithelium. Peak shedding occurred just after dawn, and trough levels occurred during the middle of the dark phase. In constant darkness, mice exhibited circadian rhythms of locomotor activity, the characteristics of which were similar between strains. Both strains also exhibited rhythmic disk shedding in constant darkness, although amplitudes of the rhythms were damped. Exogenous melatonin delivered once per day failed to reestablish high-amplitude cyclic shedding in mice held in constant darkness. Our results show that, while disk shedding in cyclic light is robustly rhythmic, neither rhythmic production of melatonin nor the circadian oscillator responsible for rhythmic locomotor activity is sufficient to drive high-amplitude rhythmic shedding in constant darkness. More importantly, melatonin is required neither for cyclic changes in the rate of disk shedding in cyclic light, nor for the circadian rhythm of disk shedding in constant darkness.

Type
Research Article
Copyright
© 1999 Cambridge University Press

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