Identification of an optimal concentration of platelet gel for promoting angiogenesis in human endothelial cells

Transfusion. 2009 Apr;49(4):771-8. doi: 10.1111/j.1537-2995.2008.02033.x. Epub 2008 Dec 23.

Abstract

Background: Numerous studies have supported the use of topical blood components to improve wound healing and tissue regeneration. Platelet gel (PG), a hemocomponent obtained from mix of activated platelets (PLTs) and cryoprecipitate, is currently being used clinically in an attempt to improve tissue healing. The present study sought to define the most effective PG concentration to promote angiogenesis in vitro.

Study design and methods: The effects of PG-released supernatant at different concentrations on human endothelial cells were studied using different in vitro assays (proliferation, migration, invasion, cord formation, and wound healing).

Results: The concentration of PG-released supernatant had a significant influence on the angiogenic potential of endothelial cells. The optimal concentration for the stimulation of angiogenesis was 1.5 x 10(6) PLTs per microL in most of the in vitro experiments used in this study. Lower or higher concentrations of PG displayed a lower angiogenic potential.

Conclusion: An optimal concentration of PG to promote angiogenesis in human endothelial cells was identified. Excessively high PG concentrations may inhibit the angiogenic process, thereby being counterproductive for wound healing in a clinical setting.

Publication types

  • Evaluation Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blood Platelets / chemistry
  • Blood Platelets / metabolism
  • Blood Platelets / physiology*
  • Cell Adhesion / drug effects
  • Cell Culture Techniques
  • Cell Movement / drug effects
  • Cell Proliferation / drug effects
  • Cells, Cultured
  • Culture Media, Conditioned / metabolism
  • Culture Media, Conditioned / pharmacology
  • Endothelial Cells / drug effects*
  • Endothelial Cells / physiology
  • Gels / pharmacology*
  • Humans
  • Male
  • Mice
  • NIH 3T3 Cells
  • Neovascularization, Physiologic / drug effects*
  • Osmolar Concentration

Substances

  • Culture Media, Conditioned
  • Gels