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作 者:韩小霞[1] 惠延年[1] 宋虎平[1] 王海涛[2] 张自峰[1]
机构地区:[1]第四军医大学西京医院眼科全军眼科研究所,中国陕西省西安市710032 [2]第四军医大学西京医院血液科,中国陕西省西安市710032
出 处:《国际眼科杂志》2006年第3期596-598,共3页International Eye Science
摘 要:目的:观察曲安奈德(TA)对高浓度葡萄糖条件下体外培养人视网膜色素上皮(hRPE)细胞细胞间黏附分子-1(I-CAM-1)表达的影响。方法:用MTT方法检测不同浓度(0.01,0.10和1.00g/L)的TA对hRPE细胞增生的影响,用免疫荧光法检测加用和未加用0.10g/LTA的30.0mmol/L葡萄糖作用1,2和3d后hRPE细胞表面ICAM-1的表达强度。结果:在0.01~1.00g/L浓度TA的作用下,hRPE细胞生长受到抑制,呈剂量依赖性和时间依从性。加用0.10g/LTA的30.0mmol/L葡萄糖作用1,2和3d后,hRPE细胞表面荧光染色密度分别比未加用TA的30.0mmol/L葡萄糖作用下荧光着色减弱20%,25%和50%,有统计学显著性差异(P<0.05)。结论:TA可以抑制体外高浓度葡萄糖培养的hRPE细胞的增生,也抑制高糖作用下hRPE细胞表面的ICAM-1表达。AIM: To investigate the effects of triamcinolone acetonide (TA)on the expression of intercelluar adhesion molecule-1 ( I- CAM-I) of human retinal pigment epithelial (hRPE) cells cultured with high glucose in vitro. METHODS: The effect of TA at various concentrations (0.01, 0.10 or 1.00g/L) on the proliferation of hRPE cells was detected by methyl thiazolyl tetrazolial (MTr) assay. The expression of ICAM-1 of hRPE cells cultured with 30.0mmol/L of glucose with or without 0.1g/L of TA for 1, 2, and 3d was measured with immunofluorescence staining. RESULTS: At the concentrations of 0.01, 0.10, or 1.00g/L of TA inhibited the growth of hRPE cells in a dose-dependent manner (P〈0.05, compared with the control), and the fluorescence staining density on the cell membrane of hRPE cells cultured with 0.1g/L of TA and with 30.0mmol/L of glucose for 1, 2 and 3d was decreased by 20%, 25%, and 50% of that without TA in 30.0mmol/L of glucose, respectively. The difference between the two groups was statistically significant (P〈0.05). CONCLUSION: TA can inhibit the growth of hRPE cells in vitro with high glucose, hRPE cells cultured with high glucose can enhance expression of ICAM-1 of the cells and that can be inhibited by TA. It is suggested that TA may interrupt pathological reaction of diabetic retinopathy by inhibiting expression of ICAM-I of hRPE cells.
关 键 词:人视网膜色素上皮细胞 高浓度葡萄糖糖 细胞间黏附分子-1 曲安奈德
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