Journal: Antioxidants
Article Title: Aldo-Keto Reductase 1C15 Characterization and Protection in Ischemic Brain Injury
doi: 10.3390/antiox12040909
Figure Lengend Snippet: AKR1C15 expression in rat primary CNS cell cultures before and after OGD. AKR1C15 mRNA in primary rat CNS cell cultures was determined by real-time PCR. ( A ) Baseline AKR1C15 expression levels compared to TAT-AKR1C15 plasmid (Biomatik). Data are mean ± SD. n = 6–9 independent experiments. One-way ANOVA followed by Tukey’s multiple comparison. *, *** p < 0.05, 0.001 vs. Neuron. ns: not significant. Cell cultures were then subjected to OGD/reoxygenation, and AKR1C15 mRNA expressions were detected at 2, 8, and 24 h after reoxygenation in cultured ( B ) neurons (1 h OGD), ( C ) OPCs (90 min OGD), ( D ) astrocytes (4 h OGD), ( E ) BMVECs (12 h OGD), and ( F ) microglia (90 min OGD). Data are mean ± SD. n = 4–9 independent experiments. One-way ANOVA followed by Tukey’s multiple comparison. *, **, *** p < 0.05, 0.01, 0.001 vs. Ctrl. OGD: oxygen–glucose deprivation. BMVEC: brain microvascular endothelial cell. OPC: oligodendrocyte precursor cell.
Article Snippet: Primary rat brain microvascular endothelial cells (BMVECs) were purchased from Cell Applications (San Diego, CA, USA) and were maintained in rat brain endothelial cell growth medium consisting of basal medium and appropriate growth factors (Cell Applications, San Diego, CA, USA).
Techniques: Expressing, Real-time Polymerase Chain Reaction, Plasmid Preparation, Comparison, Cell Culture