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作 者:宋鄂[1] 王瑜[1,2] 王秋利[3] 董宇[1] 鞠胜[4] 毕明超[1]
机构地区:[1]吉林大学第一医院眼科,长春130021 [2]南京医科大学眼科医院,210029 [3]吉林大学第四医院眼科,长春130011 [4]辽源市中医院眼科,136200
出 处:《眼科研究》2009年第1期1-4,共4页Chinese Ophthalmic Research
基 金:国家自然科学基金资助(30571992)
摘 要:目的观察缺氧、高糖及高胰岛素对视网膜Mller细胞胞浆内血管内皮生长因子(VEGF)表达的影响。方法采用组织块悬浮贴壁法原代培养兔视网膜Mller细胞,于正常和缺氧条件下分别分为对照组、高糖组、高浓度胰岛素组、高糖高浓度胰岛素组,通过AO/EB染色法观察不同缺氧时相Mller细胞的凋亡情况,免疫细胞化学染色测定各组Mller细胞胞浆内VEGF的表达。结果免疫细胞化学技术测定结果显示缺氧条件下1、2、3d各实验组与对照组相比VEGF表达量增加差异均有统计学意义(P<0.05)。缺氧2d、3d各实验组与正常条件下各实验组相比VEGF表达增加,差异均有统计学意义(P<0.05)。结论缺氧条件下高糖及高胰岛素环境刺激Mller细胞VEGF表达作用增强。Objective Retinal neovascularization is a main cause of blindness in diabetic retinopathy. Our previous study has proved the overexpression of VEGF in Maller cells in high glucose and insulin environment,but its mechanism is still unclear. This study was to investigate the change of VEGF released by cultured rabbit retinal MUller cells at high concentration glucose and high concentration insulin under hypoxia environment in vitro. Methods Rabbit' s retina was cultured by tissue suspension culture method to establish the primary culture system to obtain and identify the cultured Mailer cells by GFAP stain. Three gas incubator and low-flow sustained ventilation was used to control hypoxia environment. The cultured Mailer cells were digested by 0.25% trypsin and suspensed in H-DMEM containing 10% fetal bovine serum and then were treated under the hypoxia and further under the 50 mmol/L of glucose,4 μmol/( min·L) insulin or 50 mmol/L glucose + 4 μmol/( min·L) insulin condition respectively for 1 day,2 days and 3 days. The AO/EB stain was used to detect apoptotic Mailer cells in different time points. Immunocytochemical stain was adopted to observe the effects of hypoxia, high concentration of glucose and high concentration of insulin on expression of VEGF in the Mailer cells. Results 95% positive Maller cells for GFAP were obtained. The apoptotic Mailer cells were 20% and 32% in the 3rd and 4th days under the hypoxia. The expression of VEGF in MUller cells was significantly increased in 50 mmol/L glucose and 4 μmol/( min·L) insulin,50 mmol/L glucose + 4 μmol/ ( min·L) insulin group under the normoxia condition ( P 〈 0. 05 ,P 〈 0. 01 ). The statistically significant difference in VEGF expression was found between only hypoxic group and normal in the 2nd and 3rd day( P 〈 0. 05 ). Conclusion High concentration of glucose or high concentration of insulin can stimulate VEGF expression more obviously under the hypoxia than normoxia condition.
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