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皮质神经毒性星形胶质细胞具有早期肌萎缩侧索硬化症病理学和 miR-146a 缺陷,复制症状性 SOD1G93A 小鼠模型的神经胶质标志物。

Cortical Neurotoxic Astrocytes with Early ALS Pathology and miR-146a Deficit Replicate Gliosis Markers of Symptomatic SOD1G93A Mouse Model.

机构信息

Research Institute for Medicines (iMed.ULisboa), Faculty of Pharmacy, Universidade de Lisboa, Av. Professor Gama Pinto, 1649-003, Lisbon, Portugal.

Unit of Neurosciences, the Institute for Molecular Medicine, Universidade de Lisboa, Lisbon, Portugal.

出版信息

Mol Neurobiol. 2019 Mar;56(3):2137-2158. doi: 10.1007/s12035-018-1220-8. Epub 2018 Jul 11.

Abstract

Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease characterized by motor neuron (MN) loss. Recent evidences highlight astrocytes as important players in MN death, but the mechanism-based neurotoxicity is still unknown. It is also unclear whether activation of astrocytes in ALS occurs differently in the cerebral cortex and spinal cord. We investigated glial and neuronal alterations in the cortex of SOD1G93A (mSOD1) mice in pre-symptomatic and symptomatic stages. We also characterized astrocytes isolated from the cortex of 7-day-old mSOD1 mice for their aberrancy and MN-induced degenerative effects. In the early stage, we identified a reduction of cell proliferation, NF-kB expression, and of vimentin and micro(miR)-146a expression, suggesting a restrained cortical inflammatory status. However, increased NF-kB expression, cell proliferation, and gene expression of HMGB1, connexin 43 and S100B were distinctive of the symptomatic stage, together with MN loss, downregulated unfold protein response, and decreased expression of synaptic proteins, together with that of miR-125b, miR-21, miR-146a, GFAP, and glutamate transporters. Astrocytes cultured for 13 days in vitro showed comparable NF-kB expression and cell proliferation increase, as well as similar microRNA and gene/protein expression profiles (decreased miR-21, miR-146a, GLT-1 and GFAP, and upregulated HMGB1, S100B and connexin-43), thus sustaining astrocytes as the major contributors of cortical homeostasis deregulation in the symptomatic stage. These reactive astrocytes reduced neurite length and synaptophysin expression in NSC-34/hSOD1WT MN-like cells, and induced mitochondria dysfunction, PSD-95 downregulation, metalloproteinase-9 activation, and late apoptosis in NSC-34/hSOD1G93A cells. Data indicate that astrocytes in mSOD1 mice model acquire early phenotypic aberrancies and highlight downregulated miR-146a as a biomarker and drug target in ALS.

摘要

肌萎缩侧索硬化症(ALS)是一种致命的神经退行性疾病,其特征是运动神经元(MN)丧失。最近的证据强调了星形胶质细胞作为 MN 死亡的重要参与者,但基于机制的神经毒性仍然未知。目前也不清楚 ALS 中星形胶质细胞的激活是否在大脑皮层和脊髓中存在不同。我们研究了 SOD1G93A(mSOD1)小鼠皮层中的神经胶质和神经元变化,这些小鼠处于前症状和症状阶段。我们还对来自 7 天大的 mSOD1 小鼠皮层的星形胶质细胞进行了表型鉴定及其对 MN 诱导的退行性变化的影响。在早期阶段,我们发现细胞增殖、NF-kB 表达以及波形蛋白和 micro(miR)-146a 表达减少,表明皮质炎症状态受到抑制。然而,在症状期,NF-kB 表达、细胞增殖、HMGB1、连接蛋白 43 和 S100B 的基因表达增加,同时伴有 MN 丢失、未折叠蛋白反应下调以及突触蛋白表达减少,包括 miR-125b、miR-21、miR-146a、GFAP 和谷氨酸转运体。体外培养 13 天的星形胶质细胞表现出相似的 NF-kB 表达和细胞增殖增加,以及相似的 microRNA 和基因/蛋白表达谱(下调 miR-21、miR-146a、GLT-1 和 GFAP,上调 HMGB1、S100B 和连接蛋白 43),因此星形胶质细胞是症状期皮层内环境失调的主要贡献者。这些反应性星形胶质细胞减少 NSC-34/hSOD1WT MN 样细胞的轴突长度和突触小体蛋白表达,并诱导 NSC-34/hSOD1G93A 细胞中线粒体功能障碍、PSD-95 下调、金属蛋白酶 9 激活和晚期凋亡。数据表明,mSOD1 小鼠模型中的星形胶质细胞获得了早期表型异常,并强调下调的 miR-146a 作为 ALS 的生物标志物和药物靶点。

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