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MicroRNAs underlying memory deficits in neurodegenerative disorders

机译:MicroRNA在神经变性障碍中的内存缺陷

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摘要

Neurodegenerative disorders are defined by neuronal loss and often associated with dementia. Understanding the multifactorial nature of cognitive decline is of particular interest. Cell loss is certainly a possibility but also an early imbalance in the complex gene networks involved in learning and memory. The small (similar to 22 nt) non-coding microRNAs play a major role in gene expression regulation and have been linked to neuronal survival and cognition. Interestingly, changes in microRNA signatures are associated with neurodegenerative disorders. In this review, we explore the role of three microRNAs, namely miR-132, miR-124 and miR-34, which are dysregulated in major neurodegenerative diseases such as Alzheimer's disease, Parkinson's disease and Huntington's disease. Interestingly, these microRNAs have been associated with both memory impairment and neuronal survival, providing a potential common molecular mechanism contributing to dementia. (C) 2016 Elsevier Inc All rights reserved.
机译:神经变性障碍由神经元损失定义,通常与痴呆症相关。了解认知下降的多因素性质是特别令人感兴趣的。细胞损失肯定是一种可能性,但也是在学习和记忆中涉及的复杂基因网络中的早期不平衡。小(类似于22nt)非编码微大罗斯在基因表达调节中起主要作用,并且已与神经元生存和认知有关。有趣的是,MicroRNA签名的变化与神经变性障碍有关。在这篇综述中,我们探讨了三个MicroRNA的作用,即miR-132,miR-124和miR-34,其在主要神经变性疾病中具有吸诵,例如阿尔茨海默病,帕金森病和亨廷顿氏病。有趣的是,这些MicroRNAS与内存损伤和神经元生存期有关,提供潜在的常见分子机制,有助于痴呆。 (c)2016 Elsevier Inc版权所有。

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