Fig. 2From: KLF4 alleviates cerebral vascular injury by ameliorating vascular endothelial inflammation and regulating tight junction protein expression following ischemic strokeIncreased expression of three cell adhesion molecules and KLF4 following focal cerebral ischemia. a Images show IF staining for three cell adhesion molecules (E-selectin, VCAM-1, and ICAM-1) and KLF4 in ischemic hemisphere from sham-operated mice (S, control) or mice at day 1, 2, 4, 7, and 14 post-ischemia. Scale bar = 100 μm. b Quantification of E-selectin, VCAM-1 and ICAM-1, and KLF4 expressions. Results are expressed as the mean ± standard deviation of the number of positive events per field of view (n = 6 per experimental group). Note that cerebral ischemia induced a strong increase in the expression of all the three cell adhesion molecules in both ischemic penumbra and core, reaching a peak at day 2 and then declining at day 4. While in the ischemic penumbra, the number of KLF4-positive events increased slightly during the first 2 days post-ischemia, but then increased significantly by day 4, and reached a maximum between 7 and 14 days post-ischemia. However, in the ischemic core, the number of KLF4-positive events increased markedly during the first 2 days post-ischemia, before declining at day 4. *P < 0.05, **P < 0.01, ***P < 0.001 compared with controlBack to article page