西式饮食可增加淀粉样变性小鼠模型的脑代谢和适应性免疫反应。

IF 9.3 1区 医学 Q1 IMMUNOLOGY
Marilena Poxleitner, Sabrina H L Hoffmann, Georgy Berezhnoy, Tudor M Ionescu, Irene Gonzalez-Menendez, Florian C Maier, Dominik Seyfried, Walter Ehrlichmann, Leticia Quintanilla-Martinez, Andreas M Schmid, Gerald Reischl, Christoph Trautwein, Andreas Maurer, Bernd J Pichler, Kristina Herfert, Nicolas Beziere
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引用次数: 0

摘要

饮食引起的体重增加是全球日益关注的健康问题。饮食引起的变化往往伴随着改变全身功能的低度代谢炎症,可能也会导致神经退行性疾病的进展。本研究旨在对阿尔茨海默病 APPPS1 小鼠模型大脑中饮食诱导的代谢和炎症效应进行非侵入性研究。在野生型和 APPPS1 小鼠体内使用[18F]FDG、[18F]FTHA 和 [18F]GE-180 进行 PET 成像。体外流式细胞术和大脑组织学补充了体内研究结果。肝脏中的 1H-磁共振波谱、血浆代谢组学和白色脂肪组织的流式细胞术被用来确认外周的元炎症状况。我们发现APPPS1小鼠在摄入西方饮食后,葡萄糖和脂肪酸代谢紊乱,神经胶质依赖性神经炎症只发生了很小的区域性变化。进一步的体内外研究发现,西方饮食喂养的小鼠大脑中有细胞毒性 T 细胞参与,血浆代谢组也受到破坏。1H-试剂共振光谱和免疫学结果显示,肝脏和脂肪组织中存在饮食依赖性炎症样失衡。我们的多模态成像研究强调了脑-肝-脂肪轴和适应性免疫系统在阿尔茨海默病淀粉样蛋白模型脑平衡破坏中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Western diet increases brain metabolism and adaptive immune responses in a mouse model of amyloidosis.

Diet-induced increase in body weight is a growing health concern worldwide. Often accompanied by a low-grade metabolic inflammation that changes systemic functions, diet-induced alterations may contribute to neurodegenerative disorder progression as well. This study aims to non-invasively investigate diet-induced metabolic and inflammatory effects in the brain of an APPPS1 mouse model of Alzheimer's disease. [18F]FDG, [18F]FTHA, and [18F]GE-180 were used for in vivo PET imaging in wild-type and APPPS1 mice. Ex vivo flow cytometry and histology in brains complemented the in vivo findings. 1H- magnetic resonance spectroscopy in the liver, plasma metabolomics and flow cytometry of the white adipose tissue were used to confirm metaflammatory condition in the periphery. We found disrupted glucose and fatty acid metabolism after Western diet consumption, with only small regional changes in glial-dependent neuroinflammation in the brains of APPPS1 mice. Further ex vivo investigations revealed cytotoxic T cell involvement in the brains of Western diet-fed mice and a disrupted plasma metabolome. 1H-magentic resonance spectroscopy and immunological results revealed diet-dependent inflammatory-like misbalance in livers and fatty tissue. Our multimodal imaging study highlights the role of the brain-liver-fat axis and the adaptive immune system in the disruption of brain homeostasis in amyloid models of Alzheimer's disease.

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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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