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Published online before print September 20, 2007
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From the Institute for Radiological Imaging Science* and the Departments of Pathology¶ and Vascular and Transplantation Surgery,
Wonkwang University School of Medicine, Jeonbuk, Korea; the Department of Vascular Surgery,
Good Gang-An Hospital, Pusan, Korea; the Biomedical Research Center and Department of Biological Sciences,|| Korea Advanced Institute of Science and Technology, Daejeon, Korea; and the Department of Molecular and Cellular Biology,
Harvard University, Cambridge, Massachusetts
The present study examined the effects of cartilage oligometric matrix protein angiopoietin-1 (COMP-Ang1) on the revascularization of mice skin grafts. Full-thickness skin grafts were autotransferred into BALB/c mice. The donor grafts were soaked in COMP-Ang1 protein (50 µg/ml, n = 10) or in bovine serum albumin (BSA) (50 µg/ml, n = 10) dissolved in 1 ml of sterile, phosphate-buffered saline for 5 minutes before transfer. Revascularization of the grafts was monitored using an intravital microscope on postoperative days 3, 4, and 5. Morphological and immunohistochemical analyses were performed to evaluate platelet-endothelial cell adhesion molecule-1 and survivin expression and apoptotic signal in the transplanted grafts. Grafts soaked in COMP-Ang1 (COMP-Ang1 group) showed significantly increased revascularization compared with grafts soaked in BSA (BSA group) on intravital microscopy and platelet-endothelial cell adhesion molecule-1 staining. The COMP-Ang1 group showed a significant increase of survivin expression in the endothelial cells and a reduction of apoptotic signal in comparison to the BSA group. Therefore, we believe that COMP-Ang1 provides the therapeutic benefit of enhancing the survival of vascular endothelial cells during transplantation of skin graft.
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