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首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Transient forebrain ischemia alters the mRNA expression of methyl DNA-binding factors in the adult rat hippocampus.
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Transient forebrain ischemia alters the mRNA expression of methyl DNA-binding factors in the adult rat hippocampus.

机译:短暂性前脑缺血会改变成年大鼠海马中甲基DNA结合因子的mRNA表达。

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摘要

We have examined how transient cerebral ischemia affects the mRNA expression of a family of methyl CpG-binding domain (MBD)-containing factors in the rat hippocampus. Our results show that each member of this family is affected by cerebral ischemia challenge, but with differing patterns of responsiveness. At 3, 6 and 12 h following reperfusion, MeCP2 and MBD1 expression is maintained at control levels throughout the hippocampus. At 24 h, MeCP2 and MBD1 are induced in both the CA1 and CA3 subfields. This delayed pattern of induction is in contrast to the responses of MBD2 and MBD3. Both MBD2 and MBD3 display significant changes in expression at early times following reperfusion, although their changes are opposite in direction. MBD2 expression is induced throughout the hippocampal formation at 6 h, and remains elevated at 12 and 24 h. MBD3 expression decreases as early as 3 h following insult in the CA3 and dentate gyrus, and the decreased expression remains in the vulnerable CA1 subfield at 6, 12, and 24 h.Taken together, these results are the first to illustrate that the expression of methyl DNA-binding factors are affected by challenges to the brain, and they also illustrate that each methyl DNA-binding factor responds differently to cerebral ischemic challenge. As each of these family members is associated either directly or indirectly with the inhibition of gene transcription, our results suggest that following cerebral ischemia the normal pattern of transcriptional inhibition provided by these factors may be altered in the hippocampus.
机译:我们已经检查了短暂性脑缺血如何影响大鼠海马中的一个包含甲基CpG结合域(MBD)的因子家族的mRNA表达。我们的结果表明,该家族的每个成员都受到脑缺血攻击的影响,但反应方式不同。在再灌注后3、6和12小时,整个海马体中的MeCP2和MBD1表达维持在对照水平。在24小时时,在CA1和CA3子域中都感应到MeCP2和MBD1。这种延迟的感应模式与MBD2和MBD3的响应相反。尽管MBD2和MBD3的方向相反,但它们在再灌注后的早期都显示出明显的表达变化。 MBD2表达在6 h诱导整个海马形成,并在12和24 h保持升高。在侵害CA3和齿状回后3小时,MBD3的表达降低,而在6、12和24 h脆弱的CA1子域中仍保留了降低的表达。这些结果首次证明了甲基DNA结合因子受大脑挑战的影响,它们还说明每种甲基DNA结合因子对脑缺血挑战的反应不同。由于这些家族成员中的每一个都直接或间接与基因转录的抑制有关,因此我们的结果表明,在脑缺血后,这些因子提供的转录抑制的正常模式可能会在海马中发生改变。

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