基于ribotag的RNA分析揭示了自身免疫性脑脊髓炎中少突胶质细胞谱系特异性炎症:对发病机制的影响。

IF 9.3 1区 医学 Q1 IMMUNOLOGY
Yuhang Wang, Sudeep Ghimire, Ashutosh Mangalam, Zizhen Kang
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引用次数: 0

摘要

少突胶质谱系细胞(OLCs)是髓鞘形成、再髓鞘形成和神经元代谢支持所必需的,但最近的证据表明它们也在神经炎症中发挥积极作用。本研究旨在通过基于ribotag的RNA测序,确定实验性自身免疫性脑脊髓炎(EAE)发病期间OLCs的炎症翻译组,EAE是一种广泛应用于多发性硬化症(MS)的模型。我们将RiboTag小鼠与Olig2-Cre小鼠杂交,在OLCs中获得HA标记的核糖体蛋白Rpl22的菌株特异性表达,从而能够从这些细胞中分离出核糖体相关mRNA,并使用HA珠进行测序。与对照组相比,EAE OLCs中有1556个基因上调,683个基因下调。基因富集揭示了免疫相关通路的升高,包括细胞因子信号、干扰素反应和抗原呈递,而下调的基因与髓鞘形成和神经元发育有关。值得注意的是,在OLCs中检测到细胞因子/趋化因子及其受体的显著表达。进一步的研究集中在IFNGR和IFNAR在EAE发病机制中的作用。OLCs中的IFN-γ信号通过增强抗原加工、递呈和趋化因子的产生(如Ccl2、Ccl7),加剧了EAE的发病机制。相比之下,IFN-β信号似乎不那么关键。这些发现强调了OLCs在EAE中的炎症作用,表明OLCs是缓解MS及相关疾病神经炎症的潜在治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
RiboTag-based RNA profiling uncovers oligodendroglial lineage-specific inflammation in autoimmune encephalomyelitis: implications for pathogenesis.

Oligodendroglial lineage cells (OLCs) are essential for myelination, remyelination and neuronal metabolic support, but recent evidence suggests they also play active roles in neuroinflammation. This study aimed to identify the inflammatory translatome of OLCs during the onset of experimental autoimmune encephalomyelitis (EAE), a widely used model for Multiple Sclerosis (MS), using RiboTag-based RNA sequencing. We crossed RiboTag mice with Olig2-Cre mice to obtain strain-specific expression of HA-tagged ribosomal protein Rpl22 in OLCs, enabling the isolation of ribosome-associated mRNA from these cells for sequencing by using HA beads. Compared to controls, 1,556 genes were upregulated and 683 were downregulated in EAE OLCs. Gene enrichment revealed elevated immune-related pathways, including cytokine signaling, interferon responses and antigen presentation, whereas downregulated genes were associated with myelination and neuronal development. Notably, significant expression of cytokines/chemokines and their receptors was detected in OLCs. Further investigations focused on the role of IFNGR and IFNAR in EAE pathogenesis. IFN-γ signaling in OLCs exacerbated EAE pathogenesis by enhancing antigen processing, presentation, and chemokine production (e.g., Ccl2, Ccl7). In contrast, IFN-β signaling appeared less critical. These findings highlight the inflammatory role of OLCs in EAE, suggesting OLCs as a potential therapeutic target for mitigating neuroinflammation in MS and related disorders.

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来源期刊
Journal of Neuroinflammation
Journal of Neuroinflammation 医学-神经科学
CiteScore
15.90
自引率
3.20%
发文量
276
审稿时长
1 months
期刊介绍: The Journal of Neuroinflammation is a peer-reviewed, open access publication that emphasizes the interaction between the immune system, particularly the innate immune system, and the nervous system. It covers various aspects, including the involvement of CNS immune mediators like microglia and astrocytes, the cytokines and chemokines they produce, and the influence of peripheral neuro-immune interactions, T cells, monocytes, complement proteins, acute phase proteins, oxidative injury, and related molecular processes. Neuroinflammation is a rapidly expanding field that has significantly enhanced our knowledge of chronic neurological diseases. It attracts researchers from diverse disciplines such as pathology, biochemistry, molecular biology, genetics, clinical medicine, and epidemiology. Substantial contributions to this field have been made through studies involving populations, patients, postmortem tissues, animal models, and in vitro systems. The Journal of Neuroinflammation consolidates research that centers around common pathogenic processes. It serves as a platform for integrative reviews and commentaries in this field.
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