| Objective Skin and soft tissue expansion stimulates the proliferation of skin epidermal basal cells and increase the dermal collagen deposition and angiogenesis. To explore the contribution of bone marrow-derived stem cells (BMSCs) to the generation of "new" skin during the expansion, we used a chimeric mouse model in which the donor C57BL mice were engrafted with the bone marrow of enhanced green fluorescent protein (EGFP) transgenic mice.Methods Bone marrow-derived stem cells were collected from the tibia and femur of EGFP+ transgenic mice, and then injected into normal C57BL mice via the tail vein (Chimeric Mice). The Chimeric mice were randomized into groups A, B and C. Silicone expanders were implanted in the backs of the Group A mice and then were injected with normal saline (N.S.); silicone expanders were also implanted in the backs of the Group B mice but the expanders were not injected with N.S.; and no expanders were implanted in the Group C mice. Skin was obtained at different times (day 0,7,14,21,28 and 35). Skin Stromal-Derived Factor-1(SDF-1) expression was evaluated. The number, distribution and phenotype changes of EGFP+ cells in the skin were also evaluated by means of fluorescent microscopy.Results EGFP+ cells were present stably in the normal skin. The number of EGFP+ cells of the Group A mice changed with the tension, and reached the peak on day 21(17.1±6.7%), as compared with either Group B (5.5±1.0%) or Group C(5.1±0.9%). The SDF-1 expression in the expanded skin was significant increased (≈11-fold, p<0.01) compared to non-expanded skin on day 21. Immunofluorescence showed EGFP+ cells were converted into vascular endothelial cells, epidermal cells and spindle-shaped dermal fibroblasts.Conclusion Strain can promote the expression of SDF-1 and facilitate the differentiation and proliferation of bone marrow-derived stem cells in the expanded skin. |