Repopulation of dentin surfaces by periodontal ligament cells and endothelial cells. Effect of basic fibroblast growth factor

• Published in: Journal of periodontology (1970) Vol. 60; no. 6; p. 293
• Main Authors: Terranova, V P, Odziemiec, C, Tweden, K S, Spadone, D P
• Format: Journal Article
• Language: English
• Published: United States 01.06.1989
• Subjects: Cell Division - drug effects; Cell Movement - drug effects; Cells, Cultured; Chemotaxis - drug effects; Citrates - pharmacology; Citric Acid; Dentin - drug effects; Dentin - physiology; DNA - biosynthesis; Endothelium, Vascular - cytology; Fibroblast Growth Factors - pharmacology; Fibronectins - pharmacology; Humans; Microbial Collagenase - pharmacology; Mitogens; Periodontal Ligament - cytology; Tetracycline - pharmacology
• ISSN: 0022-3492
• DOI: 10.1902/jop.1989.60.6.293

The regeneration of connective tissue attachment is a major goal of clinical periodontics. Recent investigations on biochemically mediated periodontal regeneration have attempted to define the various biological response modifiers which may provide a mechanism for periodontal regeneration. Fibronectin and endothelial cell growth factor have been shown to selectively enhance periodontal ligament (PDL) cell adhesion, migration, and proliferation. In addition, dentin preconditioned with tetracycline HCl (TTC) or citric acid (CA) supports PDL cell adhesion, presumably by exposing collagen fibers. We have now extended these studies to include basic fibroblast growth factor (b-FGF) as a potential meditor of periodontal regeneration. Using AFSCM (assays for specific cell migration), b-FGF in concentrations as low as 10 ng per dentin block significantly stimulated PDL cell chemotaxis, while the antibody against b-FGF inhibited both the chemotactic and proliferative characteristics of the mitogen. We also found that 5 ng and above of b-FGF per dentin block significantly stimulated human endothelial cell migration and proliferation. Using 125I-b-FGF, we demonstrated that the factor binds to native dentin. This binding was increased when the dentin blocks were preconditioned by TTC or CA and reduced when the dentin was subsequently treated with collagenase. 125I-b-FGF also bound with moderate affinity to a type I collagen affinity column whereas the binding to a hydroxylapatite affinity column was negligible. The combination of FN and b-FGF was a marginally more potent chemo-attractant than b-FGF alone for PDL cells.