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A MicroRNA-BDNF Negative Feedback Signaling Loop in Brain: Implications for Alzheimer's Disease

机译:脑中的MicroRNA-BDNF负反馈信号回路:对阿尔茨海默氏病的影响

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MicroRNAs (miRNAs) are small non-coding RNAs that regulate gene expression posttranscriptionally by interfering with translation of their target mRNAs. Typically, miRNAs bind to the 3' UTRs of mRNAs to induce repression or degradation. Neurotrophins are growth factors in brain required for neuronal survival, synapse formation, and plasticity mechanisms. Neurotrophins are not only regulated by miRNAs, but they in turn regulate miRNA expression. Accumulating data indicate there is a regulatory negative feedback loop between one ubiquitous neurotrophin, brain-derived neurotrophic factor (BDNF), and miRNAs. That is, while BDNF treatment stimulates neuronal miRNA expression, miRNAs generally function to inhibit expression of BDNF. This negative feedback loop is maintained in a state of equilibrium in normal cells. However, in Alzheimer's Disease (AD), a progressive neurodegenerative disorder resulting in memory loss and eventually dementia that is characterized by reduced levels of BDNF in brain, the balance between BDNF and miRNA is shifted toward inhibitory control by miRNAs. Here, we will briefly review the evidence for a positive action of BDNF on miRNA expression and a negative action of miRNAs on BDNF. We propose that the reduction in BDNF that occurs in the AD brain is the result of two independent mechanisms: 1) a failure in the proteolytic conversion of BDNF precursor protein to its functional mature form, and 2) inhibition of BDNF gene expression by miRNAs. The role of miRNAs in BDNF regulation should be considered when developing BDNF-based therapeutic treatments for AD.
机译:MicroRNA(miRNA)是小的非编码RNA,可通过干扰其靶mRNA的翻译来调节转录后的基因表达。通常,miRNA与mRNA的3'UTR结合以诱导阻遏或降解。神经营养蛋白是大脑中神经元生存,突触形成和可塑性机制所需的生长因子。神经营养蛋白不仅受miRNA调节,而且反过来又调节miRNA的表达。越来越多的数据表明,一种普遍存在的神经营养蛋白,脑源性神经营养因子(BDNF)和miRNA之间存在调节性负反馈回路。即,虽然BDNF治疗刺激神经元miRNA表达,但是miRNA通常起到抑制BDNF表达的作用。该负反馈回路在正常细胞中保持平衡状态。然而,在阿尔茨海默氏病(AD)中,进行性神经退行性疾病导致记忆力丧失,最终导致痴呆,其特征是脑中BDNF水平降低,因此BDNF和miRNA之间的平衡已朝着miRNA的抑制控制转移。在这里,我们将简要回顾BDNF对miRNA表达的正作用和miRNA对BDNF负作用的证据。我们提出,AD脑中BDNF的降低是两个独立机制的结果:1)BDNF前体蛋白向其功能成熟形式的蛋白水解转化失败,以及2)miRNA抑制BDNF基因表达。在开发基于BDNF的AD治疗方法时,应考虑miRNA在BDNF调节中的作用。

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