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载脂蛋白E基因敲除小鼠动脉粥样硬化病变定量的实际评估

Practical assessment of the quantification of atherosclerotic lesions in apoE⁻/⁻ mice.

作者信息

Lin Yan, Bai Liang, Chen Yulong, Zhu Ninghong, Bai Yanping, Li Qianwei, Zhao Sihai, Fan Jianglin, Liu Enqi

机构信息

Laboratory Animal Center, School of Medicine, Xi'an Jiaotong University, Xi'an, Shaanxi 710061, P.R. China.

Shaanxi Key Laboratory of Ischemic Cardiovascular Disease, Institute of Basic and Translational Medicine, Xi'an Medical University, Xi'an, Shaanxi 710021, P.R. China.

出版信息

Mol Med Rep. 2015 Oct;12(4):5298-306. doi: 10.3892/mmr.2015.4084. Epub 2015 Jul 16.

Abstract

Genetic manipulations have enabled the mouse to be widely used as an animal model for investigating the mechanisms of human atherosclerotic disease. However, there is no standard method for quantifying atherosclerotic lesions among different laboratories. The present study introduces a thorough and precise quantitative assessment of atherosclerotic lesions in mice. In the present study, 6‑week‑old apoE‑/‑ mice were fed either a chow diet or a high‑fat diet (HFD) for 12 weeks. Plasma lipid levels were measured every four weeks. Aortic atherosclerotic lesions were quantified and analyzed using an image analysis system. The aortic tree was isolated and stained with Oil Red O to measure the gross lesion area. The heart was removed and divided into sequential cross sections, which were then assessed for microscopic intimal lesions in the aortic root as follows: (1) Elastic van Gieson staining was performed to determine the area of the atherosclerotic lesion; (2) cross sections were stained with hematoxylin and eosin for histological analysis; and (3) cross sections were stained with Oil Red O and immunohistochemical staining for quantitative analysis of the cellular components within the lesions. ApoE‑/‑ mice fed with either the chow diet or HFD developed severe atherosclerosis in the aortic root, however, there were few lesions in the remainder of the aortic tree. Compared with the control group, the HFD apoE‑/‑ mice had increased plasma lipid levels and increases in the gross lesion area in the aortic tree, the microscopic lesion area in the aortic root and the number of macrophages, vascular smooth muscle cells and neutral lipids present within the lesions. HFD feeding in the apoE‑/‑ mice accelerated the development of atherosclerosis. The quantitative method described in the present study may be used to assist in future investigations of atherosclerosis in mice.

摘要

基因操作使得小鼠能够广泛用作研究人类动脉粥样硬化疾病机制的动物模型。然而,不同实验室之间尚无量化动脉粥样硬化病变的标准方法。本研究引入了一种对小鼠动脉粥样硬化病变进行全面且精确的定量评估方法。在本研究中,6周龄的载脂蛋白E基因敲除(apoE⁻/⁻)小鼠被喂食普通饮食或高脂饮食(HFD)12周。每四周测量一次血浆脂质水平。使用图像分析系统对主动脉粥样硬化病变进行量化和分析。分离主动脉树并用油红O染色以测量大体病变面积。取出心脏并切成连续的横截面,然后对主动脉根部的微观内膜病变进行如下评估:(1)进行弹性范吉森染色以确定动脉粥样硬化病变的面积;(2)横截面用苏木精和伊红染色进行组织学分析;(3)横截面用油红O和免疫组织化学染色对病变内的细胞成分进行定量分析。喂食普通饮食或HFD的apoE⁻/⁻小鼠在主动脉根部出现了严重的动脉粥样硬化,然而,主动脉树的其余部分几乎没有病变。与对照组相比,HFD喂养的apoE⁻/⁻小鼠血浆脂质水平升高,主动脉树的大体病变面积、主动脉根部的微观病变面积以及病变内巨噬细胞、血管平滑肌细胞和中性脂质的数量均增加。apoE⁻/⁻小鼠喂食HFD加速了动脉粥样硬化的发展。本研究中描述的定量方法可用于辅助未来对小鼠动脉粥样硬化的研究。

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