超声波刺激调节小胶质细胞 M1/M2 极化并影响阿尔茨海默病小鼠模型的海马蛋白质组变化

IF 3.1 4区 医学 Q3 IMMUNOLOGY
Xinliang Lu, Wenxian Sun, Li Leng, Yuting Yang, Shuting Gong, Qi Zou, Haijun Niu, Cuibai Wei
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引用次数: 0

摘要

背景:已有研究报道了超声刺激治疗阿尔茨海默病(AD)的有效性,但其潜在机制仍不清楚。本研究探讨了超声刺激对不同表型小胶质细胞的比例和功能以及炎症因子水平的影响。此外,研究还揭示了超声刺激治疗后小鼠海马蛋白质组分子的变化,旨在发现潜在的新分子机制:方法:采用超声波刺激海马,超声波刺激组每天刺激海马30分钟,连续5天。采用免疫荧光染色法测量淀粉样斑块沉积。用免疫荧光双重染色法标记 M1 和 M2 型小胶质细胞,并计算其比例。使用 ELISA 试剂盒测定 Aβ42、IL-10 和 TNF-α 的水平。采用定量蛋白质组学方法探讨海马蛋白质的分子变化:结果:超声刺激治疗降低了淀粉样蛋白斑块的平均荧光强度和Aβ42的浓度。与AD组相比,超声刺激使M1小胶质细胞的比例减少了14%,M2小胶质细胞的比例增加了12%。超声刺激组中抗炎因子IL-10的浓度显著增加。蛋白质组学分析显示,超声刺激处理组和 AD 组之间有 753 个不同表达的蛋白质,其中大部分富集在线粒体的氧化磷酸化途径中。此外,参与氧化磷酸化的细胞色素c氧化酶的活性在超声刺激处理后也有所增加:结论:超声波刺激可影响 APP/PS1 小鼠的小胶质细胞极化,减少淀粉样斑块负荷,提高抗炎因子水平。蛋白质组学分析揭示了超声刺激治疗后海马蛋白质的分子变化。超声刺激诱导的小胶质细胞极化调节机制可能与线粒体氧化磷酸化的变化有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Ultrasound Stimulation Modulates Microglia M1/M2 Polarization and Affects Hippocampal Proteomic Changes in a Mouse Model of Alzheimer's Disease

Ultrasound Stimulation Modulates Microglia M1/M2 Polarization and Affects Hippocampal Proteomic Changes in a Mouse Model of Alzheimer's Disease

Background

The effectiveness of ultrasound stimulation in treating Alzheimer's disease (AD) has been reported in previous studies, but the underlying mechanisms remain unclear. This study investigated the effects of ultrasound stimulation on the proportion and function of microglia of different phenotypes, as well as on the levels of inflammatory factors. Additionally, it revealed the alterations in proteomic molecules in the mouse hippocampus following ultrasound stimulation treatment, aiming to uncover potential new molecular mechanisms.

Methods

Ultrasound stimulation was used to stimulate the hippocampus for 30 min per day for 5 days in the ultrasound stimulation-treated group. Amyloid plaque deposition was measured using immunofluorescence staining. M1 and M2 type microglia were labeled using immunofluorescent double staining, and the ratio was calculated. The levels of Aβ42, IL-10, and TNF-α were determined using ELISA kits. The quantitative proteomics method was employed to explore molecular changes in hippocampal proteins.

Results

Ultrasound stimulation treatment reduced the average fluorescence intensity of amyloid plaques and the concentration of Aβ42. Compared to the AD group, ultrasound stimulation resulted in a 14% reduction in the proportion of M1 microglia and a 12% increase in the proportion of M2 microglia. The concentration of the anti-inflammatory factor IL-10 was significantly increased in the ultrasound stimulation-treated group. Proteomics analysis revealed 753 differentially expressed proteins between the ultrasound stimulation-treated and AD groups, with most being enriched in the oxidative phosphorylation pathway of mitochondria. Additionally, the activity of cytochrome c oxidase, involved in oxidative phosphorylation, was increased after ultrasound stimulation treatment.

Conclusions

Ultrasound stimulation affects microglial polarization, reduces amyloid plaque load, and enhances levels of anti-inflammatory factors in APP/PS1 mice. Proteomics analysis reveals molecular changes in hippocampal proteins after ultrasound stimulation treatment. The mechanism behind ultrasound stimulation-induced modulation of microglial polarization may be related to changes in mitochondrial oxidative phosphorylation.

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来源期刊
Immunity, Inflammation and Disease
Immunity, Inflammation and Disease Medicine-Immunology and Allergy
CiteScore
3.60
自引率
0.00%
发文量
146
审稿时长
8 weeks
期刊介绍: Immunity, Inflammation and Disease is a peer-reviewed, open access, interdisciplinary journal providing rapid publication of research across the broad field of immunology. Immunity, Inflammation and Disease gives rapid consideration to papers in all areas of clinical and basic research. The journal is indexed in Medline and the Science Citation Index Expanded (part of Web of Science), among others. It welcomes original work that enhances the understanding of immunology in areas including: • cellular and molecular immunology • clinical immunology • allergy • immunochemistry • immunogenetics • immune signalling • immune development • imaging • mathematical modelling • autoimmunity • transplantation immunology • cancer immunology
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