Kuo Yuan1, Chun-Liang Chen, Ming T Lin. 1. Periodontics Division, Department of Dentistry, National Cheng Kung University Hospital, Tainan, Taiwan.
Abstract
OBJECTIVES: Angiogenesis is one of the most critical events in the wound healing process. Any increase in angiogenesis could result in more rapid and complete healing. A recent study found that enamel matrix derivative (EMD) could accelerate early periodontal wound healing. We wanted to clarify whether EMD caused an angiogenic effect and, thus, possibly enhanced wound healing. METHODS: We performed in vitro proliferation and chemotaxis assays on human umbilical vein endothelial cell (HUVEC) cultures, and a tissue culture assay using blood vessel fragments in fibrin gel. Collagen membranes soaked with EMD were implanted subcutaneously in mice to test the in vivo angiogenic effect. RESULTS: While there were no significant differences between the negative control and EMD groups in the proliferation assay, EMD treatment did exhibit a significantly greater dose-dependent chemotactic effect on HUVEC than control group treatments. The tissue culture in fibrin gel showed new blood vessel outgrowths in the EMD groups, but none in the negative control group. In the animal studies, significantly more endothelial cells were detected in the EMD group of mice. CONCLUSIONS: Our findings show that EMD does exhibit some angiogenic effects. However, the underlying molecules and mechanisms are still unidentified. We discuss several possibilities.
OBJECTIVES: Angiogenesis is one of the most critical events in the wound healing process. Any increase in angiogenesis could result in more rapid and complete healing. A recent study found that enamel matrix derivative (EMD) could accelerate early periodontal wound healing. We wanted to clarify whether EMD caused an angiogenic effect and, thus, possibly enhanced wound healing. METHODS: We performed in vitro proliferation and chemotaxis assays on human umbilical vein endothelial cell (HUVEC) cultures, and a tissue culture assay using blood vessel fragments in fibrin gel. Collagen membranes soaked with EMD were implanted subcutaneously in mice to test the in vivo angiogenic effect. RESULTS: While there were no significant differences between the negative control and EMD groups in the proliferation assay, EMD treatment did exhibit a significantly greater dose-dependent chemotactic effect on HUVEC than control group treatments. The tissue culture in fibrin gel showed new blood vessel outgrowths in the EMD groups, but none in the negative control group. In the animal studies, significantly more endothelial cells were detected in the EMD group of mice. CONCLUSIONS: Our findings show that EMD does exhibit some angiogenic effects. However, the underlying molecules and mechanisms are still unidentified. We discuss several possibilities.
Authors: Sofia Almqvist; Maria Werthén; Anna Johansson; Magnus S Agren; Peter Thomsen; S Petter Lyngstadaas Journal: J Mater Sci Mater Med Date: 2009-12-10 Impact factor: 3.896
Authors: Amir Haze; Angela L Taylor; Stefan Haegewald; Yoav Leiser; Boaz Shay; Eli Rosenfeld; Yael Gruenbaum-Cohen; Leah Dafni; Bernd Zimmermann; Kristiina Heikinheimo; Carolyn W Gibson; Larry W Fisher; Marian F Young; Anat Blumenfeld; Jean P Bernimoulin; Dan Deutsch Journal: J Cell Mol Med Date: 2009-02-17 Impact factor: 5.310