Figure 1
Figure 1. MC-specific deletion of HS. Pdgfrb Cre line specificity detected by ROSA26 eYFP expression (A) and (B) in embryonic skin (n = 2). Colabeling of embryonic hindbrains of Pdgfrb Cre ROSA26 EYFP at E10.5 with isolectin B4 (red, C) revealed PC-specific expression of eYFP (green, C,D); n = 4. Sections of E13.5 embryos were stained with an antibody directed against the HS chain (green), NG2 (red), and 4,6-diamidino-2-phenylindole. Vascular smooth muscle cells (vSMCs) of the dorsal aorta (E,F) have strongly reduced HS deposition with residual HS on the outermost layer of vSMCs in EXT1MCko embryos (arrow, F). Immunostaining revealed loss of HS in vSMCs and PCs of EXT1MCko (F,H), whereas HS is strongly expressed in control littermates (E,G) and localized at the abluminal surface of MCs. High magnification imaging of capillaries in the embryonic skin (I-L) showed colocalization of HS and NG2 in control sections (arrows, I.J), whereas NG2-positive cells in EXT1MCko sections lack HS (arrows, K,L).

MC-specific deletion of HS.Pdgfrb Cre line specificity detected by ROSA26 eYFP expression (A) and (B) in embryonic skin (n = 2). Colabeling of embryonic hindbrains of Pdgfrb Cre ROSA26 EYFP at E10.5 with isolectin B4 (red, C) revealed PC-specific expression of eYFP (green, C,D); n = 4. Sections of E13.5 embryos were stained with an antibody directed against the HS chain (green), NG2 (red), and 4,6-diamidino-2-phenylindole. Vascular smooth muscle cells (vSMCs) of the dorsal aorta (E,F) have strongly reduced HS deposition with residual HS on the outermost layer of vSMCs in EXT1MCko embryos (arrow, F). Immunostaining revealed loss of HS in vSMCs and PCs of EXT1MCko (F,H), whereas HS is strongly expressed in control littermates (E,G) and localized at the abluminal surface of MCs. High magnification imaging of capillaries in the embryonic skin (I-L) showed colocalization of HS and NG2 in control sections (arrows, I.J), whereas NG2-positive cells in EXT1MCko sections lack HS (arrows, K,L).

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