Quantification of total and perfused blood vessels in murine skin autografts using a fluorescent double-labeling technique
S O'Ceallaigh, SE Herrick, JE Bluff… - Plastic and …, 2006 - journals.lww.com
S O'Ceallaigh, SE Herrick, JE Bluff, DA McGrouther, MWJ Ferguson
Plastic and reconstructive surgery, 2006•journals.lww.comBackground: Two theories exist regarding the revascularization of skin autografts: direct
anastomosis between graft vessels and bed vessels, and ingrowth of bed vessels
(angiogenesis) into the graft. This study characterizes revascularization, spatially and
chronologically, in a murine skin autograft model using a double-labeling technique.
Methods: Full-thickness (1 cm 2) skin grafts were performed on adult male C57/Bl6 mice.
After 48 hours, 60 hours, 3 days, 5 days, and 14 days (n= 3 mice per time point) terminal …
anastomosis between graft vessels and bed vessels, and ingrowth of bed vessels
(angiogenesis) into the graft. This study characterizes revascularization, spatially and
chronologically, in a murine skin autograft model using a double-labeling technique.
Methods: Full-thickness (1 cm 2) skin grafts were performed on adult male C57/Bl6 mice.
After 48 hours, 60 hours, 3 days, 5 days, and 14 days (n= 3 mice per time point) terminal …
Abstract
Background:
Two theories exist regarding the revascularization of skin autografts: direct anastomosis between graft vessels and bed vessels, and ingrowth of bed vessels (angiogenesis) into the graft. This study characterizes revascularization, spatially and chronologically, in a murine skin autograft model using a double-labeling technique.
Methods:
Full-thickness (1 cm 2) skin grafts were performed on adult male C57/Bl6 mice. After 48 hours, 60 hours, 3 days, 5 days, and 14 days (n= 3 mice per time point) terminal intracardiac perfusion with a fluorescein/dextran dye demonstrated vascular filling of graft blood vessels. Fluorescence immunohistochemistry of CD31+ endothelial cells allowed counting of total vessels and fluorescein perfusion quantification of patent vessels in the lateral graft area, central graft area, graft bed, and wound margins.
Results:
Initial filling of graft vessels was seen after 48 hours. This included vessels in the papillary dermis of the graft, and there was no significant difference in the percentage of filled vessels in the deep dermis of the graft compared with the papillary dermis of the graft. A rapid increase in vessel filling was seen between 48 and 60 hours in all areas of the graft. Vessel filling occurred mainly in the central area of the graft rather than in the lateral areas.
Conclusions:
The short time course of vessel filling indicates that the initial onset of revascularization is attributable to early anastomoses between graft and bed vessels, mainly in the central area of the graft. These findings have implications for both autograft revascularization in a clinical setting and in the development of tissue-engineered skin substitutes.
Lippincott Williams & Wilkins