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. 2019 Nov 26;116(51):26029–26037. doi: 10.1073/pnas.1912178116

Fig. 1.

Fig. 1.

Mild hypoxic stress triggers vascular leak in spinal cord blood vessels associated with microglial clustering. Frozen sections of lumbar spinal cord taken from mice exposed to normoxia or 7-d hypoxia (8% O2) were stained for the following markers: the endothelial marker CD31 (Alexa Fluor 488) and fibrinogen (Cy-3) (A); fibrinogen (Cy-3) and Mac-1 (Alexa Fluor 488) (C); CD31 (Alexa Fluor 488), fibrinogen (abbreviated to Fbg in E) Cy-5 (blue) and Mac-1 (Cy-3) (D and E); and Mac-1 (Alexa Fluor 488) (F). (B) Quantification of the number of leaky (fibrinogen-positive) vessels/FOV. (G) Quantification of the morphological categorization of microglia under different conditions. Results are expressed as the mean ± SEM (n = 6 mice per group). *P < 0.05, **P < 0.01 vs. normoxic conditions. One-way ANOVA followed by Tukey’s multiple comparison test. Note that CMH induced transient vascular leak in spinal cord blood vessels that was associated with wrapping of Mac-1–positive microglial processes around the damaged vessel (high power images in E) and with morphological switch from ramified to activated morphology (F). (Scale bars, 50 μm; except for E, 25 μm.)