Chaudhuri Amrita Datta, Yelamanchili Sowmya V, Fox Howard S
Department of Pharmacology and Experimental Neuroscience, University of Nebraska Medical Center, Omaha, Nebraska, United States of America.
PLoS One. 2013 Nov 11;8(11):e79579. doi: 10.1371/journal.pone.0079579. eCollection 2013.
Aberrant expression of microRNAs (miRs) has been implicated in the pathogenesis of several neurodegenerative disorders. In HIV-associated neurocognitive disorders (HAND), miR-142 was found to be upregulated in neurons and myeloid cells in the brain. We investigated the downstream effects of chronic miR-142 upregulation in neuronal cells by comparing gene expression in stable clones of the human neuroblastoma cell line BE(2)M17 expressing miR-142 to controls. Microarray analysis revealed that miR-142 expression led to a reduction in monoamine oxidase (MAO) A mRNA, which was validated by qRT-PCR. In addition to the mRNA, the MAOA protein level and enzyme activity were also reduced. Examination of primary human neurons revealed that miR-142 expression indeed resulted in a downregulation of MAOA protein level. Although MAOA is not a direct target of miR-142, SIRT1, a key transcriptional upregulator of MAOA is, thus miR-142 downregulation of MAOA expression is indirect. MiR-142 induced decrease in MAOA expression and activity may contribute to the changes in dopaminergic neurotransmission reported in HAND.
微小RNA(miR)的异常表达与多种神经退行性疾病的发病机制有关。在与HIV相关的神经认知障碍(HAND)中,发现大脑中的神经元和髓样细胞中miR-142上调。我们通过比较表达miR-142的人神经母细胞瘤细胞系BE(2)M17稳定克隆与对照中的基因表达,研究了神经元细胞中慢性miR-142上调的下游效应。微阵列分析显示,miR-142表达导致单胺氧化酶(MAO)A mRNA减少,这通过qRT-PCR得到验证。除了mRNA,MAOA蛋白水平和酶活性也降低。对原代人神经元的检测表明,miR-142表达确实导致MAOA蛋白水平下调。虽然MAOA不是miR-142的直接靶点,但MAOA的关键转录上调因子SIRT1是,因此miR-142对MAOA表达的下调是间接的。miR-142诱导的MAOA表达和活性降低可能导致HAND中报道的多巴胺能神经传递变化。