首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Microarray expression analysis of the early N-methy-N-nitrosourea-induced retinal degeneration in rat.
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Microarray expression analysis of the early N-methy-N-nitrosourea-induced retinal degeneration in rat.

机译:早期N-甲基-N-亚硝基脲诱导的大鼠视网膜变性的微阵列表达分析。

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The study was undertaken to investigate the gene expressions in N-methy-N-nitrosourea (MNU)-induced rat retinal degeneration (RD) by performing microarray analysis of retinal RNA at 12h. All rats were randomly divided into a normal group, a 12h model group and a 24h model group. Rats in the two model groups received a single intraperitoneal injection of 40 mg/kg body weight of MNU, while those in the normal group were injected with equivalent volume of physiological saline. After 12h and 24h of the injection, rats in each respective group were sacrificed, respectively. One eye of each animal was used for hematoxylin and erosin (H&E) staining, and fresh retinas of the other eye of each animal in the both normal group and 12h model group were used to extract total RNA, which was analyzed by microarray and real time RT-PCR. Retinal histological alteration was found in the 24h model group. There were 75 genes differently expressed (ratio > or =2.0), including 64 genes up-regulated and 11 genes down-regulated. Seven genes were assayed by real time RT-PCR and demonstrated the same alteration tendency as in microarray analysis. These genes that expressed differently mainly involved signal transduction, development, immune and defense, and apoptosis, etc. The major pathways were MAP-kinase signaling pathways, Toll-like receptor signaling pathway and apoptosis pathway involved. The results suggest that there are significant changes of gene expression in the early stage of MNU-induced RD. These microarray results provide clues to understand the molecular pathways underlying photoreceptor degeneration and indicate directions for future studies.
机译:通过在12h进行视网膜RNA微阵列分析,研究了N-甲基-N-亚硝基脲(MNU)诱导的大鼠视网膜变性(RD)中的基因表达。将所有大鼠随机分为正常组,12h模型组和24h模型组。两个模型组的大鼠腹膜内注射40 mg / kg体重的MNU,而正常组的大鼠则注射等体积的生理盐水。注射12小时和24小时后,分别处死每组中的大鼠。将每只动物的一只眼睛用于苏木精和曙红(H&E)染色,并且在正常组和12h模型组中,每只动物的另一只眼睛的新鲜视网膜用于提取总RNA,并通过微阵列和实时分析RT-PCR。在24h模型组中发现视网膜组织学改变。有75种不同表达的基因(比率>或= 2.0),包括上调的64个基因和下调的11个基因。通过实时RT-PCR测定了七个基因,并证明了与微阵列分析相同的改变趋势。这些表达不同的基因主要涉及信号转导,发育,免疫和防御以及凋亡等。主要途径涉及MAP激酶信号转导通路,Toll样受体信号转导通路和凋亡通路。结果表明,在MNU诱导的RD的早期,基因表达发生了显着变化。这些微阵列结果提供线索,以了解光感受器退化的分子途径,并为今后的研究指明方向。

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