The Circadian Clock in the Retinal Pigment Epithelium Controls the Diurnal Rhythm of Phagocytic Activity

• Authors: Christopher DeVera, Morehouse School of Medicine; Jendayi Dixon, Emory University; Micah A. Chrenek, Emory University; Kenkichi Baba, Morehouse School of Medicine; Yun Z. Le, University of Oklahoma; Paul Iuvone, Emory University; Gianluca Tosini, Emory University
• Journal Title: International Journal of Molecular Sciences
• Volume: Volume 23, Number 10
• Publisher: MDPI | 2022-05-01
• Type of Work: Article | Final Publisher PDF
• Publisher DOI: http://doi.org/10.3390/ijms23105302
• Subjects: Health Sciences, Toxicology; Health Sciences, Pharmacology; Health Sciences, Opthamology
• Keywords: Science & Technology; Life Sciences & Biomedicine; Physical Sciences; Biochemistry & Molecular Biology; Chemistry, Multidisciplinary; Chemistry; retinal pigment epithelium; retina; phagocytosis; aging; circadian clocks; Bmal1; transcriptome; Photoreceptor outer segments; Gene BMAL1; Turnover; Expression; Component

Abstract

The diurnal peak of phagocytosis by the retinal pigment epithelium (RPE) of photoreceptor outer segments (POS) is under circadian control and believed that this process involves interactions from the retina and RPE. Previous studies have demonstrated that a functional circadian clock exists within multiple retinal cell types and RPE. Thereby, the aim of this study was to determine whether the clock in the retina or RPE controls the diurnal phagocytic peak and whether disruption of the circadian clock in the RPE would affect cellular function and the viability during aging. To that, we generated and validated an RPE tissue-specific KO of the essential clock gene, Bmal1, and then determined the daily rhythm in phagocytic activity by the RPE in mice lacking a functional circadian clock in the retina or RPE. Then, using electroretinography, spectral domain-optical coherence tomography, and optomotor response of visual function we determined the effect of Bmal1 removal in young (6 months) and old (18 months) mice. RPE morphology and lipofuscin accumulation was determined in young and old mice. Our data shows that the clock in the RPE, rather than the retina clock, controls the diurnal phagocytic peak. Surprisingly, absence of a functional RPE clock and phagocytic peak does not result in any detectable age-related degenerative phenotype in the retina or RPE. Thus, our results demonstrate that the circadian clock in the RPE controls the daily peak of phagocytic activity. However, the absence of the clock in the RPE does not result in deterioration of photoreceptors or the RPE during aging.