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组胺通过H受体调节人视网膜色素上皮细胞中的分子钟振荡

Histamine Regulates Molecular Clock Oscillations in Human Retinal Pigment Epithelial Cells H Receptors.

作者信息

Morioka Eri, Kanda Yuzuki, Koizumi Hayato, Miyamoto Tsubasa, Ikeda Masayuki

机构信息

Graduate School of Science and Engineering, University of Toyama, Toyama, Japan.

出版信息

Front Endocrinol (Lausanne). 2018 Mar 19;9:108. doi: 10.3389/fendo.2018.00108. eCollection 2018.

Abstract

Vertebrate eyes are known to contain circadian clocks, but their regulatory mechanisms remain largely unknown. To address this, we used a cell line from human retinal pigment epithelium (hRPE-YC) with stable coexpression of reporters for molecular clock oscillations () and intracellular Ca concentrations (). We observed concentration-dependent increases in cytosolic Ca concentrations after treatment with histamine (1-100 µM) and complete suppression of histamine-induced Ca mobilizations by H histamine receptor (HR) antagonist -chlorpheniramine (-CPA) in hRPE-YC cells. Consistently, real-time RT-PCR assays revealed that HR showed the highest expression among the four subtypes (H-H) of histamine receptors in hRPE-YC cells. Stimulation of hRPE-YC cells with histamine transiently increased nuclear localization of phosphorylated Ca/cAMP-response element-binding protein that regulates clock gene transcriptions. Administration of histamine also shifted the rhythms with a type-1 phase-response curve, similar to previous results with carbachol stimulations. Treatment of hRPE-YC cells with -CPA or with more specific HR antagonist, ketotifen, blocked the histamine-induced phase shifts. Furthermore, an H histamine receptor agonist, amthamine, had little effect on the rhythms. Although the function of the histaminergic system within the eye remains obscure, the present results suggest histaminergic control of the molecular clock HR in retinal pigment epithelial cells. Also, since -CPA and ketotifen have been widely used (e.g., to treat allergy and inflammation) in our daily life and thus raise a possible cause for circadian rhythm disorders by improper use of antihistamines.

摘要

脊椎动物的眼睛已知含有生物钟,但它们的调节机制在很大程度上仍不清楚。为了解决这个问题,我们使用了来自人视网膜色素上皮的细胞系(hRPE-YC),该细胞系稳定共表达分子钟振荡报告基因()和细胞内钙浓度()。我们观察到,在hRPE-YC细胞中,用组胺(1-100µM)处理后,胞质钙浓度呈浓度依赖性增加,并且组胺诱导的钙动员被H组胺受体(HR)拮抗剂氯苯那敏(-CPA)完全抑制。一致地,实时RT-PCR分析显示,HR在hRPE-YC细胞中组胺受体的四种亚型(H-H)中表达最高。用组胺刺激hRPE-YC细胞会短暂增加调节生物钟基因转录的磷酸化钙/环磷酸腺苷反应元件结合蛋白的核定位。给予组胺也会以1型相位反应曲线改变节律,这与之前用卡巴胆碱刺激的结果相似。用-CPA或更特异性的HR拮抗剂酮替芬处理hRPE-YC细胞可阻断组胺诱导的相位变化。此外,H组胺受体激动剂安他明对节律几乎没有影响。尽管眼内组胺能系统的功能仍不清楚,但目前的结果表明视网膜色素上皮细胞中分子钟HR受组胺能控制。此外,由于-CPA和酮替芬在我们的日常生活中已被广泛使用(例如,用于治疗过敏和炎症),因此不当使用抗组胺药可能会导致昼夜节律紊乱。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8608/5867311/b46c6b7eaa4a/fendo-09-00108-g001.jpg

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