Abstract

Many aspects of retinal photoreceptor function and physiology are regulated by the circadian clocks in these cells. It is well established that light is the primary stimulus that entrains these clocks; yet, the biochemical cascade(s) mediating light’s effects on these clocks remains unknown. This deficiency represents a significant gap in our fundamental understanding of photoreceptor signaling cascades and their functions. In this study, we utilized re-aggregated spheroid cultures prepared from embryonic chick retina to determine if activation of phospholipase C in photoreceptors in the absence of light can phase shift the melatonin secretion rhythms of these cells in a manner similar to that induced by light. We show that spheroid cultures rhythmically secrete melatonin and that these melatonin rhythms can be dynamically phase shifted by exposing the cultures to an appropriately timed light pulse. Importantly, we show that activation of phospholipase C using m-3M3FBS in the absence of light induces a phase delay in photoreceptor melatonin rhythms that mirrors that induced by light. The implication of this finding is that the light signaling cascade that entrains photoreceptor melatonin rhythms involves activation of phospholipase C.

Highlights

  • Vertebrate retinal photoreceptor physiology is intimately linked to their circadian clocks [1,2,3,4,5]

  • To identify differentiated rod and cone cells in our cultures, we stained the re-aggregated retinal cultures that had been produced from embryonic day 6 (E6) chicken retinas with antibodies directed against photoreceptor rod and cone visual pigments [33,41] and visinin, a conespecific Ca2+-binding protein expressed in chicken photoreceptors [42]

  • We demonstrate that the photoreceptors in re-aggregated, spheroid cultures prepared from embryonic chicken retinas exhibit circadian melatonin secretion rhythms that can be dynamically phase shifted by light

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Summary

Introduction

Vertebrate retinal photoreceptor physiology is intimately linked to their circadian clocks [1,2,3,4,5]. The results of this study showed that the heterotrimeric G-protein G11 is able to interact with pinopsin, the pineal opsin protein expressed in these cells, in a light- and GTP-dependent manner, and that selective activation of G11 in the absence of light induces phase shifts in the oscillators in these cells that resemble those induced by light. These authors showed that G11 is expressed in chicken retinal photoreceptors, that this protein is associated with rhodopsin in the dark, and that it dissociates from light-activated rhodopsin in a GTP-dependent manner. G11 immunoreactivity has been observed in the retinal photoreceptors of mice and cows [18]

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