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Effects of supplemental erythropoietin on its receptor expression and signal transduction pathways in rat model of retinal detachment

机译:补充促红细胞生成素对其大鼠视网膜脱离模型受体表达和信号转导通路的影响

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Purpose: The aim of this study was to investigate the effects of supplemental erythropoietin (EPO) on its receptor (EPOR) and signal transduction pathways in rat model of retinal detachment (RD). Methods: To investigate the effect of EPO on EPOR expression in RD rats 100, 200 or 400ng EPO was injected into the vitreous cavity immediately after RD model was induced. Western blot and immunohistochemistry analyses were performed to measure EPOR expression. To investigate the effect of EPO on signal transduction pathways in RD rats single dose of 400ng EPO was injected into the vitreous cavity immediately after RD model was induced. The total and phosphorylated levels of JAK2, Akt, ERK-1/2, STAT5 and NF-κB were assessed by western blot. Results: Western blot analysis showed that, compared with the normal control group, EPOR expression in the neurosensory retina was significantly increased in experimental RD groups (P<0.05), but the differences were not significant between experimental RD groups (P>0.05). Immunohistochemical examination indicated that EPOR staining on retinas became strongly positive 3 days after RD, with no significant difference in staining intensities between the treatment groups. Phosphorylated levels of JAK2, Akt, ERK-1/2, STAT5, and NF-κB were enhanced 3 days after RD, but only JAK2, Akt, and ERK-1/2 phosphorylation was further enhanced by 400ng EPO treatment (P<0.05). Conclusions: Supplementary EPO cannot affect EPOR expression in detached retina, but EPO may activate both PI-3K/Akt and MAPK/ERK-1/2 signal transduction pathways in RD model.
机译:目的:本研究的目的是研究补充性促红细胞生成素(EPO)对其大鼠视网膜脱离(RD)模型中其受体(EPOR)和信号转导途径的影响。方法:为了研究EPO对RD大鼠EPOR表达的影响,在RD模型诱导后,立即将100、200或400ng EPO注入玻璃体腔。进行蛋白质印迹和免疫组化分析以测量EPOR表达。为了研究EPO对RD大鼠信号转导途径的影响,在诱导RD模型后立即将400ng EPO单剂量注入玻璃体腔。通过蛋白质印迹法评估JAK2,Akt,ERK-1 / 2,STAT5和NF-κB的总磷酸化水平。结果:Western blot分析显示,与正常对照组相比,实验RD组神经感觉视网膜的EPOR表达明显升高(P <0.05),但实验RD组之间无显着差异(P> 0.05)。免疫组织化学检查显示,RD后3天视网膜上的EPOR染色变为强阳性,治疗组之间的染色强度无显着差异。 RD后3天,JAK2,Akt,ERK-1 / 2,STAT5和NF-κB的磷酸化水平升高,但400ng EPO处理仅进一步增强了JAK2,Akt和ERK-1 / 2的磷酸化(P <0.05 )。结论:补充EPO不能影响视网膜脱离的EPOR表达,但EPO可以激活RD模型的PI-3K / Akt和MAPK / ERK-1 / 2信号转导通路。

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