Vascular Biology |
From the Department of Internal Medicine II (M.C.I., E.G.-S., A.H., S.R.-M., I.K., H.D.G., I.M.L.), Division of Cardiology, University of Vienna, Vienna, Austria, and the Scripps Research Institute (R.R.S.), La Jolla, Calif.
Correspondence to Irene M. Lang, MD, Department of Internal Medicine II, Division of Cardiology, University of Vienna, Austria, Währinger Gürtel 18-20, 1090 Vienna, Austria. E-mail irene.lang{at}univie.ac.at
AbstractRecent information indicates that platelet-derived endothelial cell growth factor (PD-ECGF), a 45-kDa angiogenic protein, is expressed in the endothelium of various tissues and that its level of expression is correlated with the number of microvessels in human tumors. Because the formation of neovessels is also thought to play a role in atherosclerotic vascular remodeling, we analyzed PD-ECGF expression in fresh, coronary plaque tissues obtained by directional coronary atherectomy. Specimens from 31 patients were collected and analyzed by reverse transcriptionpolymerase chain reaction, histochemical staining, immunohistochemistry, and in situ hybridization with the use of PD-ECGFspecific primers and probes. Lesional vascular remodeling was assessed by intravascular ultrasound. PD-ECGF immunoreactivity and mRNA were found in plaque macrophages, endothelial cells of plaque neovessels, and stellate smooth muscle cells of 20 atherectomy specimens (64.5%). PD-ECGF immunoreactivity was correlated with the number of lesional microvessels and mast cells. Double-staining experiments revealed a close spatial proximity of PD-ECGFpositive cells and mast cells. Furthermore, the numbers of microvessels and mast cells were significantly higher in lesions lacking compensatory enlargement. The data indicate that PD-ECGF is expressed within cells of the atherosclerotic plaque and may be involved in driving angiogenesis in concert with mast cells.
Key Words: atherosclerosis angiogenesis endothelium platelet-derived factors growth substances
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