Figure 5.
Pericytes and microglial cells were present within glomeruloid bodies in the E15.5 Tfpi−/−brain. (A) Immunofluorescence of brain vasculature from littermates stained for PDGFR-β (red) and thrombomodulin (green), with DAPI-stained nuclei (blue). Occasional pericytes (red) were present along vasculature within the Tfpi+/+ brain parenchyma. The glomeruloid bodies within the Tfpi−/− embryo had numerous pericytes associated with the aggregated endothelial cells (scale bars, 10 µm). (B) Immunofluorescence of brain vasculature from littermates stained for ionized calcium-binding adapter molecule 1 (IBA1; red/yellow) and thrombomodulin (green), with DAPI-stained nuclei (blue). IBA1-expressing microglial cells were associated with endothelial cells in Tfpi+/+ and Tfpi−/− embryos, with no discernible differences between genotypes (scale bars, 10 µm).

Pericytes and microglial cells were present within glomeruloid bodies in the E15.5 Tfpi−/−brain. (A) Immunofluorescence of brain vasculature from littermates stained for PDGFR-β (red) and thrombomodulin (green), with DAPI-stained nuclei (blue). Occasional pericytes (red) were present along vasculature within the Tfpi+/+ brain parenchyma. The glomeruloid bodies within the Tfpi−/− embryo had numerous pericytes associated with the aggregated endothelial cells (scale bars, 10 µm). (B) Immunofluorescence of brain vasculature from littermates stained for ionized calcium-binding adapter molecule 1 (IBA1; red/yellow) and thrombomodulin (green), with DAPI-stained nuclei (blue). IBA1-expressing microglial cells were associated with endothelial cells in Tfpi+/+ and Tfpi−/− embryos, with no discernible differences between genotypes (scale bars, 10 µm).

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