LSU Neuroscience Center and Departments of Ophthalmology, Louisiana State University Health Sciences Center, 2020 Gravier Street, New Orleans, LA70112-2272, USA.
J Toxicol Environ Health A. 2011;74(22-24):1460-8. doi: 10.1080/15287394.2011.618973.
A mouse- and human-brain-abundant, nuclear factor (NF)-кB-regulated, micro RNA-146a (miRNA-146a) is an important modulator of the innate immune response and inflammatory signaling in specific immunological and brain cell types. Levels of miRNA-146a are induced in human brain cells challenged with at least five different species of single- or double-stranded DNA or RNA neurotrophic viruses, suggesting a broad role for miRNA-146a in the brain's innate immune response and antiviral immunity. Upregulated miRNA-146a is also observed in pro-inflammatory cytokine-, Aβ42 peptide- and neurotoxic metal-induced, oxidatively stressed human neuronal-glial primary cell cocultures, in murine scrapie and in Alzheimer's disease (AD) brain. In AD, miRNA-146a levels are found to progressively increase with disease severity and co-localize to brain regions enriched in inflammatory neuropathology. This study provides evidence of upregulation of miRNA-146a in extremely rare (incidence 1-10 per 100 million) human prion-based neurodegenerative disorders, including sporadic Creutzfeldt-Jakob disease (sCJD) and Gerstmann-Straussler-Scheinker syndrome (GSS). The findings suggest that an upregulated miRNA-146a may be integral to innate immune or inflammatory brain cell responses in prion-mediated infections and to progressive and irreversible neurodegeneration of both the murine and human brain.
一种在鼠和人脑组织中高表达、受核因子(NF)кB 调控的 micro RNA-146a(miRNA-146a),是特定免疫细胞和脑细胞固有免疫反应及炎症信号转导的重要调节因子。在受到至少五种不同种类的单链或双链 DNA 或 RNA 神经营养病毒攻击的人脑细胞中,miRNA-146a 的水平会被诱导升高,这提示 miRNA-146a 在大脑固有免疫反应和抗病毒免疫中具有广泛作用。在促炎细胞因子、Aβ42 肽和神经毒性金属诱导的、氧化应激的人源神经元-神经胶质原代细胞共培养物、鼠朊病毒病和阿尔茨海默病(AD)脑中,也观察到上调的 miRNA-146a。在 AD 中,miRNA-146a 水平随着疾病严重程度而逐渐升高,并与富含炎症性神经病理学的大脑区域共定位。本研究为 miRNA-146a 在极为罕见的(发病率为每 1 亿人中有 1-10 例)人朊病毒相关神经退行性疾病中的上调提供了证据,包括散发性克雅氏病(sCJD)和格斯特曼-施特劳斯勒-舍因克综合征(GSS)。这些发现提示,上调的 miRNA-146a 可能是朊病毒感染固有免疫或炎症性脑细胞反应以及鼠和人脑进行性和不可逆神经退行性变所必需的。