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Basic fibroblast growth factor mediates carotid plaque instability through metalloproteinase-2 and -9 expression
P Sapienza1, L di Marzo, V Borrelli
1Department of Surgery 'Pietro Valdoni', University of Rome 'La Sapienza', Rome, Italy.
Summary
Basic fibroblast growth factor (bFGF) is linked to carotid plaque instability. Higher bFGF and matrix metalloproteinase (MMP) levels in soft plaques suggest bFGF regulates MMPs, contributing to plaque instability.
Area of Science:
- Cardiovascular Research
- Biomedical Science
- Molecular Biology
Background:
- Carotid plaque instability is a significant risk factor for stroke.
- The role of basic fibroblast growth factor (bFGF) in modulating matrix metalloproteinases (MMPs) within carotid plaques remains incompletely understood.
Purpose of the Study:
- To investigate the potential role of bFGF in carotid plaque instability.
- To determine if bFGF regulates the expression and activity of MMPs in carotid plaques.
Main Methods:
- Analysis of carotid endarterectomy specimens from 40 patients, classified as soft or hard plaques.
- Measurement of serum bFGF, MMP-2, and MMP-9 levels pre- and post-operatively.
- In vitro studies using human umbilical artery smooth muscle cells (HUASMC) to assess bFGF's influence on MMP activity, production, and expression.
Main Results:
- Soft plaques exhibited significantly higher preoperative serum bFGF levels compared to hard plaques.
- Elevated serum levels and increased activity, production, and expression of MMP-2 and MMP-9 were observed in patients with soft plaques.
- In vitro experiments confirmed that bFGF directly influences the activity, production, and expression of MMP-2 and MMP-9 in HUASMC.
Conclusions:
- Basic fibroblast growth factor (bFGF) plays a crucial role in carotid plaque instability.
- bFGF appears to regulate the activity, production, and expression of matrix metalloproteinases (MMPs).
- This regulation by bFGF disrupts the normal physiological balance within carotid plaques, contributing to instability.