IADR Abstract Archives

Differential Angiogenesis between Skin and Gingival Fibroblasts During Wound Healing

Clinical observations and several evidences suggest that oral gingiva wounds heal faster and with less scarring than skin wounds. Objectives: We hypothesized that there are differences in angiogenesis pattern between skin and gingiva fibroblasts. Methods: Using a model of angiogenesis in vitro, we compared the angiogenic capacity of these cells and investigated the secretion of angiogenic growth factors by two types of fibroblasts during wound healing. Results: While both cell types promoted angiogenesis by means of soluble factors, injured gingiva fibroblasts showed an angiogenic capacity leading to the formation of capillary-like networks more important than their skin counterparts. Skin and gingival fibroblasts, either intact or after injury, were found to secrete a differential level of VEGF, FGF-2 and PDGF-AB. Intact gingival fibroblasts were found to secrete about 46 times more VEGF than their dermal counterparts.Interestingly, 5 hours after injury of gingival fibroblasts, VEGF level increased by 21% and returned to its initial value within the first day while no change was observed on its level in skin fibroblasts over 3 days. No change was observed in the secretion level of PDGF-AB after injury in both cell types. Major differences were observed with FGF-2 secretion level. Five hours after injury, gingival fibroblasts increased their secretion level by 115% while this increase in skin fibroblasts was of 291%. Conclusions: We demonstrate that there are site-specific differences in angiogenesis pattern between skin and gingival fibroblasts. Our work focuses on the role of mesenchyme in angiogenesis and its role in wound healing versus regeneration.
Division: Southeast Asian Division Meeting
Meeting: 2011 Southeast Asian Division Meeting (Singapore)
Location: Singapore
Year: 2011
Final Presentation ID: 123
Abstract Category|Abstract Category(s): Scientific Groups
Authors
  • Tran-hung, Lam  ( University of Medical Sciences - Vietnam, Ho Chi Minh City, N/A, Vietnam )
  • SESSION INFORMATION
    Oral Session
    Oral Communication Session 4
    10/29/2011