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肌萎缩侧索硬化症,脊髓前角和额叶皮质8区的基因失调:对额颞叶痴呆的影响

Amyotrophic lateral sclerosis, gene deregulation in the anterior horn of the spinal cord and frontal cortex area 8: implications in frontotemporal lobar degeneration.

作者信息

Andrés-Benito Pol, Moreno Jesús, Aso Ester, Povedano Mónica, Ferrer Isidro

机构信息

Institute of Neuropathology, Pathologic Anatomy Service, Bellvitge University Hospital, IDIBELL, Hospitalet de Llobregat, Spain.

Service of Neurology, Bellvitge University Hospital, Hospitalet de Llobregat, Spain.

出版信息

Aging (Albany NY). 2017 Mar 9;9(3):823-851. doi: 10.18632/aging.101195.

Abstract

Transcriptome arrays identifies 747 genes differentially expressed in the anterior horn of the spinal cord and 2,300 genes differentially expressed in frontal cortex area 8 in a single group of typical sALS cases without frontotemporal dementia compared with age-matched controls. Main up-regulated clusters in the anterior horn are related to inflammation and apoptosis; down-regulated clusters are linked to axoneme structures and protein synthesis. In contrast, up-regulated gene clusters in frontal cortex area 8 involve neurotransmission, synaptic proteins and vesicle trafficking, whereas main down-regulated genes cluster into oligodendrocyte function and myelin-related proteins. RT-qPCR validates the expression of 58 of 66 assessed genes from different clusters. The present results: a. reveal regional differences in de-regulated gene expression between the anterior horn of the spinal cord and frontal cortex area 8 in the same individuals suffering from sALS; b. validate and extend our knowledge about the complexity of the inflammatory response in the anterior horn of the spinal cord; and c. identify for the first time extensive gene up-regulation of neurotransmission and synaptic-related genes, together with significant down-regulation of oligodendrocyte- and myelin-related genes, as important contributors to the pathogenesis of frontal cortex alterations in the sALS/frontotemporal lobar degeneration spectrum complex at stages with no apparent cognitive impairment.

摘要

转录组阵列鉴定出,在一组无额颞叶痴呆的典型肌萎缩侧索硬化症(sALS)病例中,与年龄匹配的对照组相比,脊髓前角有747个基因差异表达,额叶皮质8区有2300个基因差异表达。脊髓前角主要上调的基因簇与炎症和细胞凋亡有关;下调的基因簇与轴丝结构和蛋白质合成有关。相比之下,额叶皮质8区上调的基因簇涉及神经传递、突触蛋白和囊泡运输,而主要下调的基因则聚集在少突胶质细胞功能和髓鞘相关蛋白方面。逆转录定量聚合酶链反应(RT-qPCR)验证了来自不同基因簇的66个评估基因中的58个基因的表达。目前的结果:a.揭示了患有sALS的同一患者脊髓前角和额叶皮质8区基因表达失调的区域差异;b.验证并扩展了我们对脊髓前角炎症反应复杂性的认识;c.首次确定神经传递和突触相关基因的广泛上调,以及少突胶质细胞和髓鞘相关基因的显著下调,是sALS/额颞叶变性谱复合体在无明显认知障碍阶段额叶皮质改变发病机制的重要因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3493/5391234/b5f8890a76a6/aging-09-823-g001.jpg

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