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作 者:朱子诚[1] 张金嵩[1] 籍雪颖[1] 王应飞[1] 陈悦[1] 李秀娟[1]
出 处:《中华眼科杂志》2007年第12期1125-1129,共5页Chinese Journal of Ophthalmology
摘 要:目的探讨豚鼠巩膜成纤维细胞中信号转导及转录活化因子3(STAT3)在胰岛素样生长因子1(IGF-1)诱导中的激活状态及其对细胞的生存及转化作用,明确在模拟近视巩膜细胞中是否存在组成性激活的STAT3信号通路。方法选用也是近视因子的IGF-1刺激豚鼠巩膜成纤维细胞后,免疫化学染色法检测细胞中STAT3及磷酸化STAT3(P-STAT3)蛋白的表达情况,RT-PCR法检测STAT3mRNA的表达;MTT法检测细胞增殖情况。结果细胞免疫化学法显示IGF-1诱导豚鼠巩膜成纤维细胞中存在激活的STAT3信号转导通路,通路蛋白STAT3、P-STAT3在细胞中均有表达(t=-6.925,-10.179,P〈0.01);半定量RT-PCR结果表明,STAT3mRNA在细胞中也存在过表达(t=9.363,P〈0.01),MTT法显示IGF-1具有促豚鼠巩膜成纤维细胞增殖作用(P〈0.05)。结论IGF-1能诱导体外培养的豚鼠巩膜成纤维细胞中STAT3信号通路的激活,提示STAT3信号通路可能在近视及巩膜重塑发生、发展中起重要作用。Objective To investigate the expression of signal transducers and activators of transcription 3 (STAT3) in sclera fibroblast of guinea pigs for understanding whether STAT3 signaling transduction pathway induced by the insulin-like growth factor-1 (IGF-1) was constitutively activated. Methods Immunocytochemical staining was used to determine the protein levels of STAT3 and P-STAT3 ( activated STAT3 ) in scleral fibroblasts. RT-PCR was used to detect the mRNA of STAT3. The effects of IGF-1 on scleral fibroblast proliferation were measured by MTr assay. Results Immunocytochemical staining and RT-PCR revealed that STAT3 protein and mRNA were over-expressed in the cells which contained constitutively activated STAT3 signaling transduction pathway (t = -6. 925, - 10. 179 and 9. 363 ; P 〈 0. 001 ). The results of MTT showed that IGF-1 induced fibroblasts proliferation significantly at concentrations of 0. 5, 1.0, 10. 0 μg/L ( P 〈 0. 05 ). Conclusion STAT3 signaling transduction pathway is constitutively activated in the treated scleral cells by IGF-1, suggesting that STAT3 signaling transduction pathway may play a critical role in the occurrence of myopia and sclera remodeling.
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