Research Article

hnRNPA2/B1 Ameliorates LPS-Induced Endothelial Injury through NF-κB Pathway and VE-Cadherin/β-Catenin Signaling Modulation In Vitro

Figure 2

Effect of hnRNPA2/B1 on endothelial permeability in HUVECs. HUVECs were transfected with hnRNPA2/B1 siRNA/negative control (NC) siRNA or pcDNA3.1(-)-Myc-6His/pcDNA3.1(-)-hnRNPA2/B1-Myc-6His plasmid for 36 h and then stimulated with 1 μg/mL LPS for different lengths of time. The hnRNPA2/B1 knockdown efficiency was determined by qRT-PCR (a) and Western blotting (b, c). The hnRNPA2/B1 overexpression efficiency was determined by Western blotting (d, e). (f, h) TEER values were measured every 2 h for 24 h of LPS stimulation. (g, i) Endothelial permeability was determined by FITC-dextran flux analysis 12 h after LPS administration. Data are expressed as (), vs. Negative control (siRNA/plasmid) , # vs. Negative control .
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