Abstract
Migration and proliferation of smooth muscle cells (SMC) in the arterial intima are well recognized features of atherosclerosis [1] and are especially prominent features of transplant atherosclerosis [2], and of restenosis after balloon angioplasty [3,4] or coronary bypass grafting [5]. The proliferation of vascular SMC may also be important in Kaposi’s sarcoma [6] and in some types of hypertension [7–10]. In atherosclerosis and in restenosis, factors implicated in the migration and proliferation of SMC include thrombi [11–13], lipoproteins [14–16], stretch [17–21], reduced flow and shear [17–21], and loss of endothelial-derived growth inhibitors [22–26]. In addition, the SMC themselves can express mitogenic vasoconstrictors [27–29], such as angiotensin, and platelet-derived growth factors (PDGFs) [30–35]. Various PDGF dimers are also released by platelets, macrophages and endothelial cells [30–35]. The possibility of a similar role for basic fibroblast growth factor (bFGF), a heparin-binding 18 kD peptide best known for its angiogenic, neurotropic, and mesoderm-inducing effects [36–38], has only recently been considered.
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Abbreviations
- aFGF:
-
acidic fibroblast growth factor
- bFGF:
-
basic fibroblast growth factor
- EGF:
-
epidermal growth factor
- PDGF:
-
platelet-derived growth factor
- FGF-R1:
-
fibroblast growth factor receptor 1 (also known as flg)
- IGF1:
-
insulin-like growth factor-1; 3HTdR: tritiated thymidine
- SMC:
-
smooth muscle cell(s)
- TGFß:
-
transforming growth factor beta
- TNF alpha:
-
tumor necrosis factor α
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Casscells, W., Lappi, D.A., Baird, A. (1993). Basic FGF’s role in smooth muscle cell proliferation: A basis for molecular atherectomy. In: Cummins, P. (eds) Growth Factors and the Cardiovascular System. Developments in Cardiovascular Medicine, vol 147. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-3098-5_13
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