CIBERNED (Network Centre for Biomedical Research of Neurodegenerative Diseases), Institute Carlos III, Ministry of Health, Madrid, Spain.
Department of Neurology, University Medical School, Göttingen, Germany.
J Mol Neurosci. 2017 Oct;63(2):206-215. doi: 10.1007/s12031-017-0971-4. Epub 2017 Sep 5.
The present study analyzes by RT-qPCR the expression of microRNA (miRNA)-27a-3p, miRNA-124-3p, miRNA-132-3p, and miRNA-143-3p in the locus coeruleus (LC), entorhinal cortex (EC), CA1 region of the hippocampus (CA1), and dentate gyrus (DG) of middle-aged (MA) individuals with no brain lesions and of cases at Braak and Braak stages I-II and II-IV of neurofibrillary tangle (NFT) pathology. The most affected region is the LC in which miRNA-27a-3p, miRNA-124-3p, and miRNA-143-3p show a trend to increase at stages I-II and are significantly up-regulated at stages III-IV when compared with MA. Only miRNA-143-3p is up-regulated in the EC at stages III-IV when compared with MA and with stages I-II. No modifications in the expression levels of miRNA-27a-3p, miRNA-124-3p, miRNA-132-3p, and miRNA-143-3p are found in CA1 at any stage, whereas miRNA-124-3p is significantly down-regulated in DG at stages I-II. Accompanying in situ hybridization reveals miRNA-27a-3p, miRNA-124-3p, and miRNA-143-3 localization in neurons, indicating that changes in miRNA expression are not a direct effect of changes in the numbers of neurons and glial cells. Present observations show for the first time important miRNA de-regulation in the LC at the first stages of NFT. Since the LC is the main noradrenergic input to the cerebral cortex, key regulator of mood and depression, and one of the first nuclei affected in aging and Alzheimer's disease (AD), these findings provide insights for additional study of the LC in aging and AD.
本研究通过 RT-qPCR 分析了无脑病变的中年个体(MA)和神经纤维缠结(NFT)病理 Braak 和 Braak I-II 期及 II-IV 期病例蓝斑(LC)、内嗅皮层(EC)、海马 CA1 区(CA1)和齿状回(DG)中 microRNA(miRNA)-27a-3p、miRNA-124-3p、miRNA-132-3p 和 miRNA-143-3p 的表达。受影响最严重的区域是 LC,其中 miRNA-27a-3p、miRNA-124-3p 和 miRNA-143-3p 在 I-II 期呈上升趋势,与 MA 相比,在 III-IV 期显著上调。只有 miRNA-143-3p 在 EC 中在 III-IV 期与 MA 和 I-II 期相比上调。在任何阶段,miRNA-27a-3p、miRNA-124-3p、miRNA-132-3p 和 miRNA-143-3p 的表达水平在 CA1 中均未发生变化,而 miRNA-124-3p 在 DG 中在 I-II 期显著下调。伴随的原位杂交显示 miRNA-27a-3p、miRNA-124-3p 和 miRNA-143-3p 在神经元中的定位,表明 miRNA 表达的变化不是神经元和神经胶质细胞数量变化的直接影响。目前的观察结果首次显示 NFT 早期 LC 中重要的 miRNA 失调。由于 LC 是大脑皮层的主要去甲肾上腺素能输入,是情绪和抑郁的关键调节剂,也是衰老和阿尔茨海默病(AD)中最早受影响的核之一,这些发现为 LC 在衰老和 AD 中的进一步研究提供了依据。