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Isolation, Processing and Analysis of Murine Gingival Cells
Published on: July 2, 2013
CD40 mediated activation of gingival and periodontal ligament fibroblasts
G D Sempowski1, P R Chess, A J Moretti
1Department of Microbiology and Immunology, University of Rochester Cancer Center, NY, USA.
Insights
CD40 is expressed on periodontal fibroblasts and its levels increase during inflammation. This interaction stimulates the production of interleukin-6 (IL-6), a key inflammatory cytokine.
Area of Science:
- Immunology
- Cell Biology
- Periodontal Medicine
Background:
- CD40 is a transmembrane protein crucial for B lymphocyte regulation.
- Its function in fibroblasts, particularly periodontal fibroblasts, was previously unknown.
- CD40 signaling is initiated by its ligand (CD40L) found on activated immune cells.
Purpose of the Study:
- To investigate the functional role of CD40 expression in periodontal fibroblasts.
- To determine if CD40 is involved in the inflammatory processes within periodontal tissues.
- To explore the signaling pathways activated by CD40 engagement in these cells.
Main Methods:
- Cultured periodontal ligament (PDL) and gingival fibroblasts were analyzed for CD40 expression.
- Interferon gamma (IFNγ) was used to modulate CD40 expression.
- Immunohistochemistry was employed to detect CD40 in gingival tissues.
- Western blot analysis assessed tyrosine phosphorylation upon CD40 triggering.
- Interleukin-6 (IL-6) production was measured following CD40 engagement.
Main Results:
- Constitutive CD40 expression was observed in both PDL and gingival fibroblasts, with higher levels in gingival cells.
- IFNγ significantly upregulated CD40 expression in both fibroblast types.
- CD40 expression was markedly increased in inflamed gingival tissue compared to normal tissue.
- CD40 engagement induced tyrosine phosphorylation and IL-6 production in gingival fibroblasts.
Conclusions:
- CD40 is an active signaling molecule in periodontal fibroblasts.
- The CD40/CD40L pathway can activate periodontal fibroblasts.
- This interaction promotes the synthesis of the pro-inflammatory cytokine IL-6, implicating CD40 in periodontal inflammation.
Abstract:
CD40 is a 50 kDa transmembrane protein important for regulating B lymphocyte proliferation and differentiation. This novel activation antigen is primarily expressed by hematopoietic cells including B lymphocytes, follicular dendritic cells, and monocytes. Recently, human fibroblasts from a variety of tissues were shown to display CD40; however, its function was unknown. Cellular responses mediated by CD40 are naturally triggered by its counter-receptor, the CD40 ligand, which is displayed on activated T cells, mast cells, eosinophils, basophils, and B lineage cells. This study investigated the functional significance of CD40 expression on periodontal fibroblasts, in the context of periodontal inflammation. The experiments reported herein demonstrate constitutive CD40 expression on cultured periodontal ligament (PDL) and gingival fibroblasts. Interestingly, cells of gingival origin displayed up to 13-fold higher constitutive levels of CD40, versus fibroblasts from PDL. Interferon gamma (IFN gamma) treatment enhanced CD40 expression on PDL and gingival fibroblasts, with up to 61-fold induction of expression. Immunohistochemical staining was used to detect CD40 on fibroblastic cells in both normal and acutely inflamed gingival tissue. Expression of CD40 in inflamed tissue was significantly higher than in uninflamed tissue. Western blot analysis of anti-CD40 triggered cells revealed the induction of tyrosine phosphorylation on a 50 kDa protein in PDL and gingival fibroblasts. These results indicate that CD40 is an active signaling conduit in periodontal fibroblasts. This concept was further substantiated by the fact that CD40 engagement stimulated interleukin 6 (IL-6) production by gingival fibroblasts, but not periodontal ligament fibroblasts. Overall, these results demonstrate that CD40 on periodontal fibroblasts may functionally interact with CD40L-expressing cells. This CD40/CD40L interaction can stimulate fibroblast activation and synthesis of the proinflammatory cytokine IL-6.
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