Figure 1
Figure 1. BMDCs do not differentiate into endothelial cells in dorsal excisional wounds. (A) The procedure for the dorsal excisional wound model combined with the GFP-bone marrow chimeric experiment. (B-H) Sectional immunohistochemistry for indicated antibodies. Grids in panels B through D indicate the fields in panels F through H, respectively. None of the CD31+ vascular endothelium is stained for GFP. (E,I) Whole-mount immunohistochemistry for indicated antibodies. A grid in panel E indicates the field in panel I. (J-K) Sectional immunohistochemistry for the tissues 7 days after wounding in Flk-1+/EGFP mice (J) or LysM-Cre/Flox-CAT-EGFP mice (K). GFP was detected only in endothelial cells of Flk-1+/EGFP mice and myeloid cells of LysM-Cre/Flox-CAT-EGFP mice. (L) FACS analysis for dissociated cells in wound tissues (day 7) of mice reconstituted with GFP+ bone marrow cells. None of GFP+ cells is positive for vascular endothelial-cadherin, and most GFP+ cells are positive for CD45. Bars represent 50 μm.

BMDCs do not differentiate into endothelial cells in dorsal excisional wounds. (A) The procedure for the dorsal excisional wound model combined with the GFP-bone marrow chimeric experiment. (B-H) Sectional immunohistochemistry for indicated antibodies. Grids in panels B through D indicate the fields in panels F through H, respectively. None of the CD31+ vascular endothelium is stained for GFP. (E,I) Whole-mount immunohistochemistry for indicated antibodies. A grid in panel E indicates the field in panel I. (J-K) Sectional immunohistochemistry for the tissues 7 days after wounding in Flk-1+/EGFP mice (J) or LysM-Cre/Flox-CAT-EGFP mice (K). GFP was detected only in endothelial cells of Flk-1+/EGFP mice and myeloid cells of LysM-Cre/Flox-CAT-EGFP mice. (L) FACS analysis for dissociated cells in wound tissues (day 7) of mice reconstituted with GFP+ bone marrow cells. None of GFP+ cells is positive for vascular endothelial-cadherin, and most GFP+ cells are positive for CD45. Bars represent 50 μm.

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