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超声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海马的蛋白质组学变化。

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

机构信息

Department of Neurology, Xuan Wu Hospital, Capital Medical University, Beijing, China.

School of Biological Science and Medical Engineering, Beihang University, Beijing, China.

出版信息

Immun Inflamm Dis. 2024 Nov;12(11):e70061. doi: 10.1002/iid3.70061.

Abstract

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.

摘要

背景

先前的研究已经报道了超声刺激在治疗阿尔茨海默病(AD)中的有效性,但潜在机制仍不清楚。本研究旨在探讨超声刺激对不同表型小胶质细胞比例和功能以及炎症因子水平的影响,并揭示超声刺激治疗后小鼠海马中的蛋白质组分子变化,以期揭示潜在的新分子机制。

方法

采用超声刺激每天刺激海马 30 分钟,连续刺激 5 天,对超声刺激治疗组进行刺激。采用免疫荧光染色法测量淀粉样斑块沉积。采用免疫荧光双重染色标记 M1 和 M2 型小胶质细胞,并计算其比例。采用 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的分子变化。

结果

超声刺激治疗降低了淀粉样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 型小胶质细胞的比例降低了 14%,M2 型小胶质细胞的比例增加了 12%。超声刺激治疗组抗炎因子 IL-10 的浓度明显升高。蛋白质组学分析显示,超声刺激治疗组和 AD 组之间有 753 个差异表达蛋白,其中大多数富集在线粒体氧化磷酸化途径中。此外,超声刺激治疗后细胞色素 c 氧化酶(参与氧化磷酸化)的活性增加。

结论

超声刺激影响小胶质细胞极化,减少 APP/PS1 小鼠的淀粉样斑块负荷,增强抗炎因子水平。蛋白质组学分析揭示了超声刺激治疗后海马蛋白的分子变化。超声刺激诱导小胶质细胞极化调节的机制可能与线粒体氧化磷酸化的变化有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/752c/11590030/344d86ad49b0/IID3-12-e70061-g002.jpg

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