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. 2019 Aug;189(8):1664–1679. doi: 10.1016/j.ajpath.2019.04.014

Figure 7.

Figure 7

Restoration of endothelial forkhead box protein M1 (Foxm1) expression in Hif1af/f/Tie2Cre+ (CKO) mice normalizes endothelial cell (EC) proliferation. A: Representative micrographs of immunostaining of lung sections. At 12 hours after cecal ligation and puncture (CLP), Hif1af/f/Tie2Cre+ mice were administered intravenously with liposome/Foxm1 plasmid DNA (CKO + Foxm1) or vector (CKO + Vector). Wild-type (WT) mice were also administered with vector. At 72 hours after CLP, mouse lungs were collected. Cryosections were immunostained with anti–5-bromo-2-deoxyuridine (BrdU) (green) and anti-CD31/anti–von Willebrand factor (vWF; red) antibodies. Nuclei were counterstained with DAPI (blue). B: Quantification of BrdU-positive ECs and non-ECs. C and D: Real-time quantitative RT-PCR analysis of expression of genes regulating cell cycle progression. Data are expressed as means ± SD (BD). ∗∗P < 0.01, ∗∗∗P < 0.001 (t-test). Scale bar = 50 μm (A).