Article Summary
徐艳春,冯婕妤,胡毅倩,朱茂林,朱 煌.900 MHz手机辐射对人视网膜色素上皮细胞增殖活性及转化生长因子β2表达的影响[J].现代生物医学进展英文版,2019,19(9):1608-1612.
900 MHz手机辐射对人视网膜色素上皮细胞增殖活性及转化生长因子β2表达的影响
Effect of 900 MHz Mobile Phone Radiation on Proliferative Activity and Expression of Transforming Growth Factor-β2 in Human Retinal Pigment Epithelium
Received:September 27, 2018  Revised:October 23, 2018
DOI:10.13241/j.cnki.pmb.2019.09.002
中文关键词: 手机  辐射  人视网膜色素上皮细胞  转化生长因子β2  眼部疾病
英文关键词: Mobile  Radiation  Human retinal pigment epithelium  Transforming growths factor-β2  Ocular disease
基金项目:上海市科委基金项目(17411950200&17411950206);上海市卫生局中医药科研基金项目(2014JP015A)
Author NameAffiliationE-mail
XU Yan-chun Department of Ophthalmology, Xinhua Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200092, China poguxibao@sjtu.edu.cn 
FENG Jie-yu Department of Ophthalmology, Xinhua Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200092, China  
HU Yi-qian Department of Ophthalmology, Xinhua Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200092, China  
ZHU Mao-lin Department of Ophthalmology, Xinhua Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200092, China  
ZHU Huang Department of Ophthalmology, Xinhua Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200092, China  
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中文摘要:
      摘要 目的:研究900 MHz手机辐射对人视网膜色素上皮细胞(RPE)增殖活性及转化生长因子β2(TGF-β2)表达的影响。方法:采用体外培养的RPE细胞,给予900 MHz手机电磁辐射者处理作为辐射组,未给予辐射者作为对照组。通过CCK8法检测RPE细胞的增殖活性,Real-Time PCR法检测RPE细胞TGF-β2 mRNA的表达,ELISA法检测RPE细胞培养上清液中TGF-β2的蛋白含量。结果:与对照组相比,辐射组RPE细胞的增殖活性降低,TGF-β2 mRNA表达增加,RPE细胞培养上清中TGF-β2含量上调,且差异具有统计学意义(P<0.05)。结论:900 MHz的手机辐射可能能通过调节TGF-β2的表达和释放导致RPE细胞增殖活性降低相关的眼部疾病。
英文摘要:
      ABSTRACT Objective: To investigate the effect of 900 MHz mobile phone radiation on the proliferative activity and expression of transforming growth factor-β2(TGF-β2) in human retinal pigment epithelium (RPE). Methods: RPE cells were cultured in vitro and di- vided into two groups. The radiation group was given exposure with a 900 MHz mobile phone in call and the control group was not given any exposure. The proliferation of RPE cells was detected by the cell-counting kit-8 (CCK8) assay. The expression of TGF-β2 mRNA and protein secretion of RPE cells were measured by Real-Time quantitative polymerase chain reaction (Real-Time PCR) and Enzyme- linked immunosorbent assay (ELISA) respectively. Results: The viability of RPE cells in radiation group was lower compared to that of the control group. The level of TGF-β2 mRNA and secretion were up-regulated under the exposure in contrast with the control group(P<0.05). Conclusion: 900 MHz mobile phone radiation may have an underlying association with some eye diseases related with de- creased proliferative activity of RPE cells by regulating the expression and release of TGF-β2.
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