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作 者:龚爱红[1] 刘志宏[1] 严青[1] 张庆峰[1] 张志远[2] 王光俊[3]
机构地区:[1]宁夏医科大学公共卫生学院,宁夏银川750004 [2]宁夏医科大学总医院医院感染科,750004 [3]宁夏银川市疾病预防控制中心传染病与免疫规划科,750001
出 处:《中国职业医学》2013年第5期398-402,共5页China Occupational Medicine
基 金:宁夏医科大学"博士学位建设学科"开放课题(KF2010-01);宁夏高等学校科学技术研究重点项目(NGY2012048);宁夏回族自治区卫生厅科研项目(2012011)
摘 要:目的探讨三磷酸肌醇受体Ⅲ型(IP3RⅢ)DNA甲基化对硫酸铍(BeSO4)致人胚肺成纤维细胞(MRC-5细胞)损伤的影响。方法建立离体细胞培养实验模型,以终浓度分别为1.0、10.0、100.0μmol/L的BeSO4染毒MRC-5细胞24 h(设为低、中、高剂量染毒组),对照组不使用BeSO4染毒。采用巢式降落式甲基化特异性聚合酶链式反应(PCR)法检测IP3RⅢDNA甲基化的变化,实时定量PCR检测IP3RⅢmRNA的表达,激光共聚焦显微镜检测细胞钙离子浓度([Ca2+]i)。结果高剂量组IP3RⅢDNA甲基化值分别低于对照组、低剂量组和中剂量组[(0.26±0.07)vs(0.48±0.02)、(0.44±0.04)、(0.37±0.03),P<0.01,P<0.01,P<0.05];低、中、高剂量组IP3RⅢmRNA表达量均高于对照组[(0.35±0.08)、(0.31±0.05)、(0.71±0.09)vs(0.03±0.01),P<0.01],高剂量组IP3RⅢmRNA表达量分别高于低、中剂量组[(0.71±0.09)vs(0.35±0.08)、(0.31±0.05),P<0.01];高剂量组细胞内[Ca2+]i平均荧光强度高于对照组[(6 171.66±601.72)vs(3 618.33±559.26),P<0.05]。结论 IP3RⅢDNA低甲基化致细胞内IP3RⅢmRNA表达增加,[Ca2+]i增加,可能是BeSO4致MRC-5细胞损伤的重要机制之一。Objective To explore the effects of inositol trisphosphate receptor Ⅲ ( IP3 R Ⅲ ) methylation in the injury of human embryonic hmg fibrobiast ( MRC-5 cell) induced by beryllium sulfate ( BeSOg ). Methods Experimental model of cell culture in vitro was established, MRC-5 cells were exposed to final concentrations of 0. 0, 1.0, 10. 0, 100. 0 μmol/L of BeSO4 for 24 hours (control-, low-, medium- and high- dose groups). DNA methylation status of IP3RⅢ was detected by nMS-polymerase chain reaction (PCR) , the expression of IP3RⅢ mRNA was detected by real-time PCR, intracellular cytoplasmic free Ca2+ concentration ([ Ca2+]i) was detected by laser scanning confocal microscope. Results IP3RⅢ DNA methylation values in high dose group were lower than those in the control, low dose and medium dose groups [ (0. 26 ±0.07) vs (0.48±0.02), (0. 44±0.04), (0.37±0.03), P〈0.01, P〈0.01, P〈0.05]. IP3R~[ mRNA expression in low, medium and high dose groups were higher than those of the control [ ( 0. 35 ±0.08 ) , ( 0. 31 ±0. 05 ) , ( 0. 71 ±0. 09) vs (0. 03 ±0. 01 ), P 〈0. 01 ]. IP3RⅢ mRNA expression in high dose group was higher than those in low and medium dose groups [ (0. 71 ±0. 09) vs (0. 35 ±0. 08 ), (0. 31 ±0. 05 ), P 〈 0. 01 1. [ Ca2 + ] i mean fluorescence intensity in high dose group was higher than that of the control group [ (6 171.66 ±601.72) vs (3 618.33 ±559. 26), P 〈 0. 05 ]. Conclusion The hypomethylation of IP3R Ⅲ DNA methylation which results in the increase of the intracellular IP3R ⅢmRNA expression and [ Ca2+] i concentrations by BeSO4 may be one important mechanism of MRC-5 injury.
关 键 词:三磷酸肌醇受体 DNA甲基化 硫酸铍 人胚肺成纤维细胞
分 类 号:R114[医药卫生—卫生毒理学] R135.1[医药卫生—公共卫生与预防医学]
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