Topic
Pinealocyte
About: Pinealocyte is a research topic. Over the lifetime, 1605 publications have been published within this topic receiving 55609 citations.
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TL;DR: The notion that melatonin signaling may be important for the regulation of clock gene expression in the inner or ganglion cells layer, but not in photoreceptors is supported.
Abstract: Previous studies have shown that retinal melatonin plays an important role in the regulation of retinal daily and circadian rhythms. Melatonin exerts its influence by binding to G-protein coupled receptors named melatonin receptor type 1 and type 2 and both receptors are present in the mouse retina. Earlier studies have shown that clock genes are rhythmically expressed in the mouse retina and melatonin signaling may be implicated in the modulation of clock gene expression in this tissue. In this study we determined the daily and circadian expression patterns of Per1, Per2, Bmal1, Dbp, Nampt and c-fos in the retina and in the photoreceptor layer (using laser capture microdissection) in C3H-f+/+ and in melatonin receptors of knockout (MT1 and MT2) of the same genetic background using real-time quantitative RT-PCR. Our data indicated that clock and clock-controlled genes are rhythmically expressed in the retina and in the photoreceptor layer. Removal of melatonin signaling significantly affected the pattern of expression in the retina whereas in the photoreceptor layer only the Bmal1 circadian pattern of expression was affected by melatonin signaling removal. In conclusion, our data further support the notion that melatonin signaling may be important for the regulation of clock gene expression in the inner or ganglion cells layer, but not in photoreceptors.
56 citations
TL;DR: The ultrastructure of pinealocytes of the mole-rat (Spalax ehrenbergi), a blind subterranean mammal living in complete darkness, was examined and compared with pinealocyte of other mammals.
Abstract: The ultrastructure of pinealocytes of the mole-rat (Spalax ehrenbergi), a blind subterranean mammal living in complete darkness, was examined and compared with pinealocytes of other mammals. Two different populations of pinealocytes (I and II) were observed. They differed in general aspect, in location and especially in their content of cell organelles involved in synthetic processes. Mitochondria, ribosomes, granular endoplasmic reticulum, lysosomes, lipid inclusions and glycogen granules were present in the perikarya of pinealocytes of both populations. In the pinealocyte of population I some granular vesicles were occasionally observed in the cell body. Their presumed origin from the Golgi apparatus could not be clearly demonstrated. In the perikaryon of this pinealocyte, concentrations of ribosomes and of cisternae of the granular endoplasmic reticulum were constantly observed. These concentrations may indicate an intensive synthetic activity. Pinealocytes of population II were characterized by accumulations of proteinaceous material in some cisternae of the granular endoplasmic reticulum and between the two layers of the nuclear membrane. The origin of these peculiar elements is discussed.
55 citations
TL;DR: It is hypothesized that rather than the peripheral circulatory melatonin circadian rhythm serving as the light/dark signal, it is the melatonin rhythm in CSF of the third ventricle that serves this purpose.
55 citations
TL;DR: Data suggested that GL enhanced chick pinealocytes and retinal cells to express AANAT mRNA and to secrete MT, which may be depended on promoting c‐Fos expression and cell proliferation.
Abstract: The goal of this study is to investigate the effects of various monochromatic lights on plasma melatonin (MT) levels and the expression of arylalkylamine N-acetyltransferase (AANAT) mRNA in the pineal gland and retina. A total of 160 newly hatched (posthatching day 1, P1) broilers, including intact, sham-operated, and pinealectomized groups were exposed to blue light (BL), green light (GL), red light (RL), and white light (WL) by light emitting diode (LED) system for short term (24 hr) or long term (2 weeks), separately. For intact and sham-operated birds, the plasma MT level exhibited marked circadian rhythms at P7 and P14 regardless of short-term and long-term exposure to four monochromatic lights. However, WL and BL showed a faint suppression of MT secretion in contrast to GL and RL at either light or dark time points, with the following rank order: GL < RL < WL < BL. Larger circadian amplitude of MT levels was observed in GL group versus BL group (at P14: 87.70 pg/mL vs. 19.85 pg/mL, respectively). Pinealectomy disturbed the MT rhythm under different light colors, especially in RL. Additionally, consistent with the alteration of plasma MT levels, we observed increased AANAT mRNA expression and immunoreactive cell numbers of proliferating cell nuclear antigen (PCNA) and c-Fos in the pineal gland or retina in GL than that of BL, whereas 5-HT immunoreactive cell number was significantly decreased in GL. These data suggested that GL enhanced chick pinealocytes and retinal cells to express AANAT mRNA and to secrete MT, which may be depended on promoting c-Fos expression and cell proliferation.
55 citations
TL;DR: One miRNA (miR182) was identified that targeted the 3'-untranslated region (3'-UTR) of Clock, a key component of clock genes, and played a crucial role in regulating CLOCK expression after oxygen-glucose deprivation in primarily cultured pinealocytes.
55 citations