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Effects of basic fibroblast growth factor on human gingival epithelial cells
Shin-ichi Takayama1, Joji Yoshida, Hiroyuki Hirano
1Department of Periodontology, Division of Oral Biology and Disease Control, Osaka University Graduate School of Dentistry, Suita, Osaka, Japan.
Journal of Periodontology
|January 28, 2003
Summary
Basic fibroblast growth factor (FGF-2) is present in gingival epithelium intercellular spaces and promotes gingival epithelial cell proliferation. This growth factor
Area of Science:
- Cell Biology
- Tissue Engineering
- Biochemistry
Background:
- Previous studies demonstrated basic fibroblast growth factor (FGF-2) impacts periodontal ligament (PDL) cell proliferation and extracellular matrix production.
- This research investigates FGF-2 expression within gingival epithelium (GE) and its influence on GE cell proliferation.
Purpose of the Study:
- To determine the expression and localization of FGF-2 in human gingival epithelium.
- To investigate the proliferative effects of FGF-2 on gingival epithelial cells in vitro.
Main Methods:
- Human GE cells were isolated and analyzed for FGF-2 and FGF receptor (FGFR) mRNA expression via RT-PCR.
- Immunohistochemistry using a novel anti-FGF-2 antibody (BF-2) was employed to detect FGF-2 distribution in gingival tissues.
- GE cell proliferation was assessed by measuring [3H]-thymidine uptake in response to FGF-2 stimulation.
Main Results:
- GE cells expressed FGFR-1, -2, -3, and -4 mRNA but not FGF-2 mRNA.
- FGF-2 was localized to intercellular spaces of the gingival epithelium, sensitive to heparitinase treatment.
- FGF-2 significantly enhanced GE cell proliferation in vitro, an effect inhibited by fetal calf serum, contrasting with synergistic enhancement in PDL cells.
Conclusions:
- FGF-2 is localized in gingival epithelial intercellular spaces, likely bound by heparan sulfate.
- FGF-2 may regulate GE cell growth and differentiation through specific cell-type receptors.
- FGF-2 exhibits cell-type specific differential effects on proliferation, notably contrasting GE and PDL cells.