Practical assessment of the quantification of atherosclerotic lesions in apoE-/- mice

被引:30
|
作者
Lin, Yan [1 ,2 ]
Bai, Liang [1 ,2 ]
Chen, Yulong [3 ]
Zhu, Ninghong [1 ,2 ]
Bai, Yanping [1 ,2 ]
Li, Qianwei [1 ,2 ]
Zhao, Sihai [1 ,2 ]
Fan, Jianglin [4 ]
Liu, Enqi [1 ,2 ,3 ]
机构
[1] Xi An Jiao Tong Univ, Sch Med, Lab Anim Ctr, Xian 710061, Shaanxi, Peoples R China
[2] Xi An Jiao Tong Univ, Res Inst Atherosclerot Dis, Xian 710061, Shaanxi, Peoples R China
[3] Xian Med Univ, Inst Basic & Translat Med, Shaanxi Key Lab Ischem Cardiovasc Dis, Xian 710021, Shaanxi, Peoples R China
[4] Univ Yamanashi, Interdisciplinary Grad Sch Med & Engn, Dept Mol Pathol, Yamanashi 4093898, Japan
基金
中国国家自然科学基金;
关键词
aorta; atherosclerosis; morphometry; mouse; E KNOCKOUT MICE; E-DEFICIENT MICE; MOUSE MODELS; HYDROGEN-SULFIDE; APOLIPOPROTEIN; PROGRESSION; RABBITS; MODIFIERS; CELLS;
D O I
10.3892/mmr.2015.4084
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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 0 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.
引用
收藏
页码:5298 / 5306
页数:9
相关论文
共 50 条
  • [41] Severity of atherosclerotic lesions in ApoE-/- mice assessed by noninvasive in vivo high resolution magnetic resonance microscopy
    Aguinaldo, JGS
    Choudhury, RP
    Rong, JX
    Yodice, C
    Fallon, JT
    Fisher, EA
    Fayad, ZA
    CIRCULATION, 2000, 102 (18) : 459 - 459
  • [42] Elucidating the mechanisms of formononetin in modulating atherosclerotic plaque formation in ApoE-/- mice
    Ying He
    Youde Cai
    Dingling Wei
    Liping Cao
    Qiansong He
    Yazhou Zhang
    BMC Cardiovascular Disorders, 24
  • [43] EFFECTS OF FCγRIIIA ON AORTIC ATHEROSCLEROTIC PLAQUE DESTABILISATION IN APOE-/- MICE
    Huang, Ye
    Yin, Huijun
    HEART, 2012, 98 : E70 - E71
  • [44] In vivo fluorescence-mediated tomography demonstrates atorvastatin promoted reduction of macrophages in atherosclerotic lesions of apoE-/-mice
    Larmann, J.
    Frenzel, T.
    Schmitz, M.
    Hahnenkamp, A.
    Demmer, P.
    Immenschuh, S.
    Tietge, U. J. F.
    Bremer, C.
    Theilmeier, G.
    EUROPEAN HEART JOURNAL, 2012, 33 : 407 - 407
  • [45] Iron Chelation by Desferrioxamine Inhibits Atherosclerotic Lesion Development in Apoe-/- Mice
    Zhang, Wei-Jian
    Wei, Hao
    Frei, Balz
    FREE RADICAL BIOLOGY AND MEDICINE, 2008, 45 : S151 - S152
  • [46] Brief Report: Increased Apoptosis in Advanced Atherosclerotic Lesions of Apoe-/- Mice Lacking Macrophage Bcl-2
    Thorp, Edward
    Li, Yankun
    Bao, Liping
    Yao, Pin Mei
    Kuriakose, George
    Rong, James
    Fisher, Edward A.
    Tabas, Ira
    ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2009, 29 (02) : 169 - U44
  • [47] Pharmacological depletion of serotonin promotes atherosclerotic plaque formation in apoE-/- mice
    Rami, M.
    Ring, L.
    Horckmans, M.
    Duchene, J.
    Megens, R.
    Soehnlein, O.
    Steffens, S.
    CARDIOVASCULAR RESEARCH, 2016, 111 : S55 - S55
  • [48] Proteomic and metabolomic analysis of atherosclerotic aortas derived from APOE-/- MICE
    Mayr, M.
    Chung, Y.
    Mayr, U.
    Troy, H.
    Griffiths, J.
    Xu, Q.
    MOLECULAR & CELLULAR PROTEOMICS, 2005, 4 (08) : S174 - S174
  • [49] Characterisation of an atherosclerotic microcalcification model using ApoE-/- mice and PET/CT
    MacAskill, Mark G.
    McDougald, Wendy
    Alcaide-Corral, Carlos
    Newby, David E.
    Tavares, Adriana A. S.
    Hadoke, Patrick W. F.
    Wu, Junxi
    IJC HEART & VASCULATURE, 2020, 31
  • [50] Oral Polystyrene Consumption Potentiates Atherosclerotic Lesion Formation in ApoE-/- Mice
    Zhao, Jingjing
    Gomes, Daniel
    Yuan, Fangping
    Feng, Jing
    Zhang, Xiang
    O'Toole, Timothy E.
    CIRCULATION RESEARCH, 2024, 134 (09) : 1228 - 1230