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阿尔茨海默病进展过程中 miRNA 网络的改变。

Alteration of the microRNA network during the progression of Alzheimer's disease.

机构信息

VIB Center for the Biology of Disease, Leuven, Belgium; Center for Human Genetics, Leuven Institute for Neurodegenerative Disorders (LIND) University Hospitals Leuven, and University of Leuven, O&N4, Herestraat, Leuven, Belgium.

出版信息

EMBO Mol Med. 2013 Oct;5(10):1613-34. doi: 10.1002/emmm.201201974. Epub 2013 Sep 9.

Abstract

An overview of miRNAs altered in Alzheimer's disease (AD) was established by profiling the hippocampus of a cohort of 41 late-onset AD (LOAD) patients and 23 controls, showing deregulation of 35 miRNAs. Profiling of miRNAs in the prefrontal cortex of a second independent cohort of 49 patients grouped by Braak stages revealed 41 deregulated miRNAs. We focused on miR-132-3p which is strongly altered in both brain areas. Downregulation of this miRNA occurs already at Braak stages III and IV, before loss of neuron-specific miRNAs. Next-generation sequencing confirmed a strong decrease of miR-132-3p and of three family-related miRNAs encoded by the same miRNA cluster on chromosome 17. Deregulation of miR-132-3p in AD brain appears to occur mainly in neurons displaying Tau hyper-phosphorylation. We provide evidence that miR-132-3p may contribute to disease progression through aberrant regulation of mRNA targets in the Tau network. The transcription factor (TF) FOXO1a appears to be a key target of miR-132-3p in this pathway.

摘要

通过对 41 名晚发性阿尔茨海默病(AD)患者和 23 名对照者的海马体进行分析,建立了 AD 中改变的 miRNA 概述,显示 35 种 miRNA 失调。对第二个独立队列的 49 名患者的前额叶皮层进行 miRNA 分析,这些患者按 Braak 分期分组,发现 41 种 miRNA 失调。我们重点研究了 miR-132-3p,它在两个脑区都有明显改变。这种 miRNA 的下调在 Braak 分期 III 和 IV 就已经发生,早于神经元特异性 miRNA 的丧失。下一代测序证实 miR-132-3p 及其三个家族相关 miRNA 的强烈减少,这些 miRNA 由 17 号染色体上的同一个 miRNA 簇编码。AD 大脑中 miR-132-3p 的失调似乎主要发生在显示 Tau 过度磷酸化的神经元中。我们提供的证据表明,miR-132-3p 可能通过对 Tau 网络中的 mRNA 靶标异常调节,导致疾病进展。转录因子(TF)FOXO1a 似乎是这条通路中 miR-132-3p 的关键靶标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3a8/3799583/f7586745257f/emmm0005-1613-f1.jpg

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