Ke Yan, Li Wentao, Tan Zhiqun, Yang Zhikuan
Aier School of Ophthalmology, Central South University, Changsha, Hunan Province, China; Institute for Memory Impairments and Neurological Disorders, University of California, Irvine, CA 92697, USA.
Aier School of Ophthalmology, Central South University, Changsha, Hunan Province, China; Institute for Memory Impairments and Neurological Disorders, University of California, Irvine, CA 92697, USA; Huizhou Third People's Hospital, Guangzhou Medical University, Huizhou, Guangdong Province, China.
Biochem Biophys Res Commun. 2017 May 6;486(3):686-692. doi: 10.1016/j.bbrc.2017.03.099. Epub 2017 Mar 20.
Dopamine is known to play an important role in the pathophysiological process of myopia development relevant to the ambient lighting, but it is still poorly understood about how lighting regulates dopamine and its interaction with dopamine receptors to mediate the pathogenic signal transduction leading to alterations of ocular globe and the pathogenesis of myopia. Many studies have highlighted changes of ocular dopamine amount in response to different lighting conditions, but little attention has been paid to the dopamine receptors during these processes. Here we examined the effects of different lighting exposures on the expression of dopamine receptors in rat R28 retinal precursor cells. R28 cells normally grown in dark were exposed to a low (10 lux) or high (500 lux) intensity of a source of LED white light (5000 K-6000 K) for 12 h and total RNA was isolated either immediately or after certain time continuous growing in dark. Both conventional and real-time RT-PCR were performed to determine the expression of all five different dopamine receptors in cells after treatments. While the transcripts of dopamine D2, D3, and D4 receptors were not detected in the total RNA preparations of all the cells, those of D1 and D5 receptors (DRD1 and DRD5) were induced by lighting in contrast to the dark control. Elevated levels of DRD1 and DRD5 mRNA returned back close to the original levels once the cells were maintained in dark after light exposures. Immunofluorescence microscopy using a specific antibody confirmed an increase in the immunoreactivity of DRD1 in the cells exposed to 500 lux lighting versus dark control. Notably, treatments of R28 cells with nanomolar dosages of dopamine (0-500 nM) directly downregulated expression of both DRD1 and DRD5, whereas haloperidol (0-50 nM), a DRD2 antagonist, significantly induced expression of DRD1. These results suggest that dopamine receptors in the retinal cells might actively respond to the environmental lighting to act as an important player in the activation of the dopaminergic system in the ocular structures relevant to the lighting-induced pathogenic development of myopia.
已知多巴胺在与环境光照相关的近视发展病理生理过程中发挥重要作用,但关于光照如何调节多巴胺及其与多巴胺受体的相互作用以介导导致眼球改变和近视发病机制的致病信号转导,仍知之甚少。许多研究强调了不同光照条件下眼内多巴胺量的变化,但在这些过程中对多巴胺受体的关注较少。在此,我们研究了不同光照暴露对大鼠R28视网膜前体细胞中多巴胺受体表达的影响。将通常在黑暗中生长的R28细胞暴露于低强度(10勒克斯)或高强度(500勒克斯)的LED白光源(5000K - 6000K)下12小时,然后立即或在黑暗中连续生长一段时间后分离总RNA。采用传统RT-PCR和实时RT-PCR来确定处理后细胞中所有五种不同多巴胺受体的表达。虽然在所有细胞的总RNA制剂中未检测到多巴胺D2、D3和D4受体的转录本,但与黑暗对照相比,D1和D5受体(DRD1和DRD5)的转录本在光照下被诱导。一旦细胞在光照后维持在黑暗中,DRD1和DRD5 mRNA的升高水平就会恢复到接近原始水平。使用特异性抗体的免疫荧光显微镜检查证实,与黑暗对照相比,暴露于500勒克斯光照的细胞中DRD1的免疫反应性增加。值得注意的是,用纳摩尔剂量的多巴胺(0 - 500 nM)处理R28细胞会直接下调DRD1和DRD5的表达,而DRD2拮抗剂氟哌啶醇(0 - 50 nM)则显著诱导DRD1的表达。这些结果表明,视网膜细胞中的多巴胺受体可能会积极响应环境光照,在与光照诱导的近视发病相关的眼结构中多巴胺能系统的激活中发挥重要作用。