摘要
背景:阿尔茨海默病(AD)是痴呆的最常见原因。作为一种异源性疾病,有几种临床和病理生物学定义的亚型具有不同的分子特征。神经炎症促成了 AD 发病机制,然而,它在 AD 异质性中所起的作用尚不清楚。目的:我们旨在说明神经炎症在 AD 异质性中的作用。 方法:进行基于转录组学、miRNOmics 和蛋白质组学的综合网络分析,以说明 AD 的异质性特征。构建并分析了组合功能网络和假设网络,以探索神经炎症在 AD 异质性中所起的作用。 结果:星形胶质细胞、小胶质细胞、“M2 巨噬细胞-神经元”和“小胶质细胞-神经元”显示以细胞和空间特异性方式富含神经炎症相关功能术语。小胶质细胞和神经元可以通过三种不同的方式相互作用,包括通过中间细胞的间接相互作用、通过可溶性因子的间接相互作用以及建立局部和功能不同信号的直接相互作用,所有这些都用于控制不同的生物过程。联合网络分析展示了神经炎症在“AD 假设网络”中的关键作用。 结论:AD异质性可能是由参与神经炎症的异质细胞和空间特异性分子特征之间的串扰引起的。
关键词: 神经炎症、异质性、阿尔茨海默病、组合网络、串扰、假设网络。
Current Alzheimer Research
Title:Systematic Characterization of Heterogeneity Caused by Neuroinflammation in Alzheimer’s Disease Based on Integrative Network Analysis
Volume: 18 Issue: 13
关键词: 神经炎症、异质性、阿尔茨海默病、组合网络、串扰、假设网络。
摘要: Background: Background: Alzheimer’s disease (AD) is the most common cause of dementia. As a heterogenous disease, there are several clinically and pathobiological defined subtypes with different molecular signatures. Neuroinflammation contributed to AD pathogenesis, however, the roles it played in the heterogeneity of AD was unclear.
Objective:We aimed to illustrate the roles neuroinflammation played in the heterogeneity of AD.
Method:An integrative network analysis based on transcriptomics, miRNOmics, and proteomics was performed to illustrate the heterogeneous characters of AD. Combined-functional-networks and hypothesis- network were constructed and analyzed to explore the roles neuroinflammation played in AD heterogeneity.
Results: Astrocytes, microglia, ‘M2 macrophage-Neuron’, and ‘Microglia- Neuron’ were shown to be enriched in neuroinflammation related functional terms in a cell- and spatial-specific way. The microglia and neurons could interact with each other in three different ways including indirect interactions via intermediate cells, indirect interactions via soluble factors, and direct interactions established localized and functionally distinct signaling, all of which were used to control different biological processes. The combined network analyses exhibited the key roles neuroinflammation plays in the ‘AD hypothesis network’.
Conclusion: The AD heterogeneity may be caused by the heterogeneous cells involved in neuroinflammation and the crosstalks between spatial-specific molecular signatures.
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Cite this article as:
Systematic Characterization of Heterogeneity Caused by Neuroinflammation in Alzheimer’s Disease Based on Integrative Network Analysis, Current Alzheimer Research 2021; 18 (13) . https://dx.doi.org/10.2174/1567205019666211216104449
DOI https://dx.doi.org/10.2174/1567205019666211216104449 |
Print ISSN 1567-2050 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-5828 |
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