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机构地区:[1]河南省立眼科医院(河南省眼科研究所),河南省郑州市450000 [2]郑州人民医院眼科,河南省郑州市450003 [3]西安市第九医院眼科,陕西省西安市710054
出 处:《眼科新进展》2017年第6期511-514,共4页Recent Advances in Ophthalmology
基 金:陕西省自然科学基础研究计划面上项目(编号:2016JM8018)~~
摘 要:目的研究脂联素(adiponectin,APN)对体外培养的猴脉络膜/视网膜内皮细胞(RF/6A)增殖、迁移和管腔形成的影响,探讨APN对脉络膜和视网膜新生血管的抑制作用。方法取体外培养的生长良好的RF/6A细胞用于实验,将细胞随机分为对照组、不同浓度重组APN组(5 pg·mL^(-1)、50 pg·mL^(-1)、500 pg·mL^(-1)预处理1 h)。培养24 h后采用MTT法检测细胞增殖,细胞划痕法检测细胞迁移,基质胶(Matrigel)法检测管腔形成。结果不同浓度重组APN组24 h的细胞增殖均弱于对照组(均为P<0.05),不同浓度重组APN组细胞24 h的迁移面积均小于对照组(均为P<0.05),不同浓度重组APN组管腔形成数均明显少于对照组(均为P<0.05),且细胞增殖、迁移和管腔形成均随着重组APN浓度的升高而降低。结论 APN能够明显抑制RF/6A细胞的血管生成过程,提示APN对于脉络膜和视网膜新生血管具有一定的保护作用。Objective To investigate the effects of adiponectin (APN) on prolif- eration, migration and tube formation of RF/6A cells, and explore the effects of APN on choroidal and retinal angiogenesis. Methods Well cultured RF/6A cells were random- ly divided into the control group and three groups with different concentrations of re- combinant adiponectin (5 pg mL-1 ,50 pg mL-1 ,500 pg mL-1 ) for 1 hour. After 24 hours, cell proliferation, migration and tube formation were detected by MTT assay, wound scratch assay and seeding cells in matrigel, respectively. Resuits The cell pro- liferation in all APN groups was weaker than that of control group ( P 〈 0.05 ), the cell migration area (pixels) of all APN groups was significantly smaller than that of the con- trol group (P 〈 0.05 ), and the number of tube formation of all APN groups was signifi- cantly less than the control group (P 〈 0.05 ). Cell proliferation, migration and tube for- mation decreased along with the increase of APN concentration. Conclusion APN can obviously inhibit the angiogenesis process of RF/6A cells. This inhibitive effect indicates the protective role of APN in choroidal and retinal angiogenesis.
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