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转铁蛋白受体 2 突变小鼠的大脑转录组紊乱支持铁过载疾病中大脑变化的情况,包括与长时程抑郁和长时程增强相关的影响。

Brain transcriptome perturbations in the transferrin receptor 2 mutant mouse support the case for brain changes in iron loading disorders, including effects relating to long-term depression and long-term potentiation.

机构信息

School of Biomedical Sciences and Pharmacy, The University of Newcastle, Callaghan, NSW, Australia.

出版信息

Neuroscience. 2013 Apr 3;235:119-28. doi: 10.1016/j.neuroscience.2013.01.014. Epub 2013 Jan 16.

Abstract

Iron abnormalities within the brain are associated with several rare but severe neurodegenerative conditions. There is growing evidence that more common systemic iron loading disorders such as hemochromatosis can also have important effects on the brain. To identify features that are common across different forms of hemochromatosis, we used microarray and real-time reverse transcription polymerase chain reaction (RT-PCR) to assess brain transcriptome profiles of transferrin receptor 2 mutant mice (Tfr2(mut)), a model of a rare type of hereditary hemochromatosis, relative to wildtype control mice. The results were compared with our previous findings in dietary iron-supplemented wildtype mice and Hfe(-/-) mice, a model of a common type of hereditary hemochromatosis. For transcripts showing significant changes relative to controls across all three models, there was perfect (100%) directional concordance (i.e. transcripts were increased in all models or decreased in all models). Comparison of the two models of hereditary hemochromatosis, which showed more pronounced changes than the dietary iron-supplemented mice, revealed numerous common molecular effects. Pathway analyses highlighted changes for genes relating to long-term depression (6.8-fold enrichment, p=5.4×10(-7)) and, to a lesser extent, long-term potentiation (3.7-fold enrichment, p=0.01), with generalized reductions in transcription of key genes from these pathways, which are involved in modulating synaptic strength and efficacy and are essential for memory and learning. The agreement across the models suggests the findings are robust and strengthens previous evidence that iron loading disorders affect the brain. Perturbations of brain phenomena such as long-term depression and long-term potentiation might partly explain neurologic symptoms reported for some hemochromatosis patients.

摘要

脑内铁异常与几种罕见但严重的神经退行性疾病有关。越来越多的证据表明,更为常见的全身性铁负荷失调,如血色病,也会对大脑产生重要影响。为了确定不同类型血色病共有的特征,我们使用微阵列和实时逆转录聚合酶链反应(RT-PCR)来评估转铁蛋白受体 2 突变(Tfr2(mut))小鼠,一种罕见遗传性血色病的模型,与野生型对照小鼠的脑转录组谱。将结果与我们之前在饮食铁补充野生型小鼠和 Hfe(-/-)小鼠(一种常见遗传性血色病的模型)中的发现进行比较。对于与所有三种模型对照相比有显著变化的转录物,有完美(100%)的方向性一致性(即所有模型中都增加或所有模型中都减少)。对两种遗传性血色病模型的比较表明,与饮食铁补充小鼠相比,这两种模型显示出更明显的变化,揭示了许多共同的分子效应。途径分析突出了与长时程抑制(6.8 倍富集,p=5.4×10(-7))和在较小程度上与长时程增强(3.7 倍富集,p=0.01)相关的基因的变化,这些基因涉及调节突触强度和效能,对记忆和学习至关重要。模型之间的一致性表明这些发现是可靠的,并加强了之前的证据,即铁负荷失调会影响大脑。脑现象如长时程抑制和长时程增强的紊乱可能部分解释了一些血色病患者报告的神经症状。

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