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Expansion of Human Peripheral Blood γδ T Cells using Zoledronate
Published on: September 9, 2011
Antigen-presenting-cell function of interferon gamma-treated human gingival fibroblasts
Y Shimabukuro1, S Murakami, H Okada
1Department of Periodontology and Endodontology, Osaka University Faculty of Dentistry, Japan.
Journal of Periodontal Research
|April 1, 1996
Summary
Human gingival fibroblasts (HGF) stimulated with IFN-gamma express HLA-DR but cannot activate naive T cells due to lack of CD80. However, these cells can stimulate primed T cells, suggesting a role in periodontal inflammation.
Area of Science:
- Immunology
- Cell Biology
- Periodontology
Background:
- Human gingival fibroblasts (HGF) are crucial in periodontal tissues.
- Antigen-presenting cells (APCs) play a key role in initiating immune responses.
- Interferon-gamma (IFN-gamma) is a cytokine involved in immune regulation.
Purpose of the Study:
- To investigate the antigen-presenting cell (APC) functions of human gingival fibroblasts (HGF) upon stimulation with IFN-gamma.
- To determine if IFN-gamma-treated HGF can stimulate T cell proliferation.
- To explore the potential role of HGF in immune responses within periodontal lesions.
Main Methods:
- Human gingival fibroblasts (HGF) were stimulated with IFN-gamma.
- Expression of HLA-DR and ICAM-1 on HGF was analyzed.
- T cell proliferation assays were performed using allo-reactive peripheral blood T cells (PBT) and primed CD4+ T cells.
- Detection of IL-1, PGE2, and CD80 expression on HGF.
- IFN-gamma mRNA levels in inflamed gingival tissue were measured.
Main Results:
- IFN-gamma stimulation induced HLA-DR and ICAM-1 expression on HGF, mimicking APC phenotype.
- IFN-gamma-treated HGF failed to induce proliferation of unprimed allo-reactive PBT.
- Lack of CD80 expression on IFN-gamma-treated HGF may explain their inability to stimulate naive T cells.
- IFN-gamma-treated HGF induced proliferation of primed allo-reactive CD4+ T cells in a HLA-DR-dependent manner.
- High levels of IFN-gamma mRNA were detected in inflamed gingival tissue.
Conclusions:
- IFN-gamma-stimulated HGF exhibit some APC characteristics but are ineffective at activating naive T cells.
- The absence of CD80 on IFN-gamma-treated HGF likely contributes to their limited APC function.
- IFN-gamma-treated HGF can stimulate pre-activated T cells, suggesting a role in modulating immune responses in periodontal inflammation.
- Locally secreted IFN-gamma may influence HGF function in inflammatory periodontal lesions.

