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* These authors contributed equally
This protocol provides a comprehensive methodology for the quantitative analysis of atherosclerotic plaques to facilitate more in-depth research into the mechanisms and progression of atherosclerosis.
Atherosclerosis, a leading cause of cardiovascular diseases, necessitates a detailed examination of lesion development and progression. This study introduces a comprehensive protocol for the isolation and histological analysis of aortic arch and root lesions in a widely used atherosclerotic mouse model, low-density lipoprotein receptor knock-out (Ldlr-/-) mice. The aortic arch and root are key sites for atherosclerotic lesions, and their examination is critical for assessing the onset, progression, or regression of atherosclerosis, predicting cardiovascular event risks, and identifying potential therapeutic targets. This protocol outlines methods for quantifying atherosclerotic burden in the aortic arch and root, including tissue isolation, fixation, Oil Red O staining, aortic root sectioning, Hematoxylin and Eosin (HE) staining, Verhoeff-Van Gieson (VVG) staining, and image analysis. Oil Red O staining measures plaque area in the aortic arch, evaluating the severity of atherosclerosis, while HE staining of the aortic root reveals plaque components such as the lipid core and fibrous cap, facilitating the assessment of plaque stability and rupture risk. VVG staining can stain collagen fibers within tissues, providing further insights into plaque composition and related information. This thorough analysis offers valuable insights into the mechanisms of lesion development and may guide the creation of novel therapeutic strategies for preventing and treating atherosclerosis.
Cardiovascular diseases, particularly atherosclerosis, have emerged as a significant health burden and a primary cause of death worldwide1,2. Atherosclerosis is a chronic progressive inflammatory disease characterized by the gradual accumulation of lipids and the formation of plaques in the arterial wall, ultimately leading to the narrowing of the arterial lumen and potentially to the rupture of plaques, triggering acute cardiovascular events such as myocardial infarction and stroke1,2,3. Given its profound impact on ....
All animal protocols used in this study were approved by the Ethics Review Committee for Animal Experimentation of the Shanghai University of Sport.
1. Preparation of reagents and dissection tools
The representative results demonstrate the application of the isolation and analysis technique for aortic arch and root lesions in an atherosclerotic mouse model. These results provide clear evidence of the technique's ability to identify and characterize atherosclerotic lesions. For example, histological images with specific stains (e.g., Oil Red O) highlight lipid accumulation, while hematoxylin and eosin (H&E) staining reveals the overall morphology of the atherosclerotic lesions, including the structure of th.......
Here, we provide detailed information on the methods of aortic sampling in Ldlr knockout mice and quantitative analysis of plaques.
The precision of the dissection procedure is the biggest technical challenge to in vivo aortic stripping in the mouse model of atherosclerosis. Based on our experience, the key points are as follows: (1) use PBS to wash out all the blood in the artery to increase the comparison between aortic arch branches and perivascular fat. (2) Be patient. Due to the .......
Nothing to declare.
This work was supported by Shanghai Frontiers Science Research Base of Exercise and Metabolic Health, the research program of exercise and public health (0831) in Shanghai University of Sport, Shanghai higher education young teachers training funding program (A2-0213-22-0058-5), and Shanghai Municipal Science and Technology Committee of Shanghai outstanding academic leaders plan (21XD1403200) for Longhua Liu.
....Name | Company | Catalog Number | Comments |
Adhesion microscope slides(25×75mm) | CITOTEST | Cat# 80312-3161 | |
Embedding cassette | CITOTEST | Cat# 80106-1100-16 | |
Eosin Staining Solution | Beyotime | Cat# C0109 | |
Ethanol | Sinopharm Chemical Reagent Co. | Cat# 10009218 | |
Hematoxylin Staining Solution | Beyotime | Cat# C0107 | |
Low-profile disposable blades | Leica | Cat# 14035838925 | |
Microscope cover glass(24×50mm) | CITOTEST | Cat# 10212450C | |
Neutral Balsam Mounting Medium | Sango Biotech | Cat# E675007-0100 | |
Oil red o powder | Sigma-Aldrich | Cat# 1320-06-5 | |
paraffin with ceresin | Sinopharm Chemical Reagent Co. | Cat# 69019461 | |
Paraformaldehyde | Servicebio | Cat# G1101 | |
Phosphate Buffered Saline (PBS, Powder) | Servicebio | Cat# G0002-2L | |
Ponceau S Staining Solution | EveryLab | Cat# FM024 | |
Victoria Blue’B | Aladdin | Cat# 2580-56-5 | |
Xylene | Sigma-Aldrich | Cat# 104-81-4 |
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