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Alpha-v beta-3 integrin expression in normal and atherosclerotic artery
M Hoshiga1, C E Alpers, L L Smith
1Department of Pathology, University of Washington, Seattle 98195, USA.
Circulation Research
|December 1, 1995
Summary
Alpha v beta 3 integrin is highly expressed in normal and atherosclerotic arteries, particularly on endothelial cells and smooth muscle cells within plaques. This finding highlights its potential role in cardiovascular disease development.
Area of Science:
- Cardiovascular Biology
- Integrin Signaling
- Atherosclerosis Research
Background:
- Alpha v beta 3 integrin is implicated in atherosclerosis and restenosis, influencing smooth muscle cell migration and angiogenesis.
- While alpha v beta 3 ligands are present in atherosclerotic plaques, its expression at these sites remains largely uncharacterized.
Purpose of the Study:
- To investigate the expression patterns of alpha v beta 3 integrin in normal and atherosclerotic human coronary arteries.
- To determine the cellular localization of alpha v beta 3 integrin within different arterial layers and plaque components.
Main Methods:
- Immunohistochemical analysis of 36 coronary artery segments from heart transplant recipients, categorized as diffuse intimal thickening (DIT) or atherosclerotic plaques.
- Utilized monoclonal antibodies against alpha v beta 3 and cell markers for smooth muscle cells (SMCs), macrophages, and endothelial cells.
- Confirmed alpha v beta 3 presence in aortic media via immunoprecipitation and RT-PCR.
Main Results:
- High alpha v beta 3 integrin expression observed on the endothelium of both DIT and plaque arteries.
- Extensive, though less intense, alpha v beta 3 expression found in the media of both artery types.
- Intimal alpha v beta 3 expression predominantly colocalized with SMCs, with minimal association with macrophages; plaque microvessels showed prominent expression.
Conclusions:
- Alpha v beta 3 integrin is widely expressed in human coronary arteries, including atherosclerotic lesions.
- Its localization on endothelial cells, smooth muscle cells, and plaque neovasculature suggests a significant role in atherosclerosis pathogenesis.
- Further research into alpha v beta 3 integrin's function in vascular disease is warranted.