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. Author manuscript; available in PMC: 2020 Nov 1.
Published in final edited form as: Hypertension. 2019 Sep 23;74(5):1113–1123. doi: 10.1161/HYPERTENSIONAHA.119.13469

Figure 4.

Figure 4.

A-B) Representative quantification (A) of renal cross sections showing co-immunoreactivity for M2 macrophages (MRC1, green), VEGFA (red), and DAPI (blue) from normal, CKD, and CKD ELP-VEGF pigs after 14 weeks of observation (n=6–7/group). B) Quantification of mean fluorescence intensity of VEGF staining in M1 and M2 macrophages. C) Representative magnified renal cross section showing glomerular cells displaying co-immunoreactivity of MRC1, VEGFA and DAPI (n=6–7/group) treated with ELP-VEGF therapy. Normal kidneys showed dispersed VEGF staining, which was attenuated in CKD. After ELP-VEGF therapy in CKD, significantly increased VEGF expression was observed predominantly inside of M2 macrophages. Although representative glomeruli are shown here, accumulation of VEGF-expressing M2 macrophages after ELP-VEGF therapy was also observed in the peritubular spaces. Scale bar: 20 μm. *p<0.05 vs. CKD M1 and CKD ELP VEGF M1; † p<0.05 vs. CKD M2 (Single way ANOVA, Tukey).