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细胞因子刺激的人皮质类器官中诱导的神经炎症的分子特征

Molecular Signature of Neuroinflammation Induced in Cytokine-Stimulated Human Cortical Spheroids.

作者信息

De Kleijn Kim M A, Straasheijm Kirsten R, Zuure Wieteke A, Martens Gerard J M

机构信息

Donders Centre for Neuroscience (DCN), Department of Molecular Animal Physiology, Faculty of Science, Donders Institute for Brain, Cognition and Behavior, Radboud University, 6525 GA Nijmegen, The Netherlands.

NeuroDrug Research Ltd., 6525 ED Nijmegen, The Netherlands.

出版信息

Biomedicines. 2022 Apr 29;10(5):1025. doi: 10.3390/biomedicines10051025.

Abstract

Crucial in the pathogenesis of neurodegenerative diseases is the process of neuroinflammation that is often linked to the pro-inflammatory cytokines Tumor necrosis factor alpha (TNFα) and Interleukin-1beta (IL-1β). Human cortical spheroids (hCSs) constitute a valuable tool to study the molecular mechanisms underlying neurological diseases in a complex three-dimensional context. We recently designed a protocol to generate hCSs comprising all major brain cell types. Here we stimulate these hCSs for three time periods with TNFα and with IL-1β. Transcriptomic analysis reveals that the main process induced in the TNFα- as well as in the IL-1β-stimulated hCSs is neuroinflammation. Central in the neuroinflammatory response are endothelial cells, microglia and astrocytes, and dysregulated genes encoding cytokines, chemokines and their receptors, and downstream NFκB- and STAT-pathway components. Furthermore, we observe sets of neuroinflammation-related genes that are specifically modulated in the TNFα-stimulated and in the IL-1β-stimulated hCSs. Together, our results help to molecularly understand human neuroinflammation and thus a key mechanism of neurodegeneration.

摘要

神经炎症过程在神经退行性疾病的发病机制中至关重要,该过程通常与促炎细胞因子肿瘤坏死因子α(TNFα)和白细胞介素-1β(IL-1β)相关。人类皮质类器官(hCSs)是在复杂的三维环境中研究神经疾病潜在分子机制的宝贵工具。我们最近设计了一种方案来生成包含所有主要脑细胞类型的hCSs。在此,我们用TNFα和IL-1β对这些hCSs进行三个时间段的刺激。转录组分析表明,在TNFα刺激的hCSs以及IL-1β刺激的hCSs中诱导的主要过程是神经炎症。神经炎症反应的核心是内皮细胞、小胶质细胞和星形胶质细胞,以及编码细胞因子、趋化因子及其受体以及下游NFκB和STAT信号通路成分的失调基因。此外,我们观察到在TNFα刺激的hCSs和IL-1β刺激的hCSs中特异性调节的一组神经炎症相关基因。总之,我们的结果有助于从分子层面理解人类神经炎症,从而理解神经退行性变的关键机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2c8/9138619/8a9965588a3e/biomedicines-10-01025-g001.jpg

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