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. Author manuscript; available in PMC: 2017 Jan 1.
Published in final edited form as: Microcirculation. 2016 Jan;23(1):75–87. doi: 10.1111/micc.12261

Figure 5.

Figure 5

Immunofluorescence staining reveals an increase in monocyte and macrophage recruitment to ligated tissue and an increase in proliferating cells in ligated tissue. A,B.) Confocal micrographs show an increase in CX3CR1-eGFP+ cells (green) in ligated tissue when compared to sham tissue. C.) Quantification of eGFP+ cells per FOV reveals an increase in eGFP+ cells in ligated tissue (p-value < 0.001, Student’s t-test). Three mice were used and four FOVs were quantified. D,E.) Confocal micrographs show an increase in CD68+ cells (blue) in ligated tissue when compared to sham tissue. F.) Quantification of CD68+ cells per FOV reveals an increase in CD68+ cells in ligated tissue in the distal region (p-value<0.01, Two-way ANOVA). Three mice were used and four FOVs were quantified. G,H.) Confocal micrographs show an increase in CD206+ cells (green) in ligated tissue when compared to sham tissue. I.) Quantification of CD206+ cells per FOV reveals an increase in CD206+ cells in ligated tissue in the distal region (p-value<0.001, Student’s t-test). Three mice were used and four FOVs were quantified. J,K.) Confocal micrographs show an increase in Ki-67+ cells (blue) in ligated tissue when compared to sham tissue. L.) Quantification of Ki-67+ cells per FOV reveals an increase in Ki-67+ cells in ligated tissue in the distal region (p-value<0.001, Student’s t-test). Three mice were used and four FOVs were quantified. Scale bars = 50 µm. Data presented are mean + standard deviation for all graphs.