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首页> 外文期刊>Japanese Journal of Ophthalmology >Involvement of the Rho/Rho kinase signaling pathway in platelet-derived growth factor BB-induced vascular endothelial growth factor expression in diabetic rat retina.
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Involvement of the Rho/Rho kinase signaling pathway in platelet-derived growth factor BB-induced vascular endothelial growth factor expression in diabetic rat retina.

机译:Rho / Rho激酶信号转导通路参与糖尿病大鼠视网膜中血小板衍生的生长因子BB诱导的血管内皮生长因子的表达。

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PURPOSE: To examine the role played by the Rho/Rho kinase pathway in the platelet-derived growth factor BB (PDGF-BB)-induced expression of vascular endothelial growth factor (VEGF) in the diabetic rat retina. METHODS: Male Sprague-Dawley rats were made diabetic by a single intraperitoneal injection of streptozotocin. Diabetic rats and PDGF-BB-exposed primary cultured porcine retinal pericyte cells (PRPCs) were treated with fluvastatin, an HMG-CoA reductase inhibitor, and fasudil, a selective Rho kinase inhibitor. The retinal expression of VEGF was determined by reverse transcriptase-polymerase chain reaction (RT-PCR). The mRNA expression of VEGF and the activation of Rho A were studied by Northern and Western blot analyses. RESULTS: RT-PCR showed that in rats that were diabetic for 4 weeks VEGF mRNA expression levels were 1.8-fold those in control rats. This enhanced expression was blocked by treatment with fluvastatin or fasudil. Exposure of PRPCs to PDGF-BB increased their VEGF mRNA expression threefold, and fluvastatin suppressed this effect. Fluvastatin also suppressed the PDGF-BB-induced activation of Rho GTPase in PRPCs. CONCLUSIONS: The Rho/Rho kinase pathway may be involved in the upregulation of VEGF expression in the diabetic retina, suggesting that fasudil might be useful for the prevention of diabetic retinopathy.
机译:目的:探讨Rho / Rho激酶途径在糖尿病大鼠视网膜中血小板衍生的生长因子BB(PDGF-BB)诱导的血管内皮生长因子(VEGF)表达中的作用。方法:通过腹膜内注射链脲佐菌素使雄性Sprague-Dawley大鼠成为糖尿病。用HMG-CoA还原酶抑制剂氟伐他汀和选择性Rho激酶抑制剂法舒地尔对糖尿病大鼠和暴露于PDGF-BB的原代培养的猪视网膜视网膜周细胞(PRPC)进行处理。通过逆转录酶-聚合酶链反应(RT-PCR)确定VEGF的视网膜表达。通过Northern和Western印迹分析研究VEGF的mRNA表达和Rho A的激活。结果:RT-PCR显示,糖尿病大鼠在4周内VEGF mRNA的表达水平是对照组的1.8倍。这种增强的表达被氟伐他汀或法舒地尔治疗所阻断。将PRPC暴露于PDGF-BB可使其VEGF mRNA表达增加三倍,而氟伐他汀可抑制该作用。氟伐他汀还抑制了PDGF-BB诱导的PRPC中Rho GTPase的活化。结论:Rho / Rho激酶途径可能参与了糖尿病视网膜VEGF表达的上调,提示法舒地尔可能对糖尿病视网膜病变的预防具有重要意义。

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