Min Han, Suresh Pendem, Suet Ling Teh, Dinesh K Sukumaran, Feng Wu, John X Wilson

PMID: 19840845 PMCID: PMC2818310 DOI: 10.1016/j.freeradbiomed.2009.10.034


Endothelial barrier dysfunction contributes to morbidity in sepsis. We tested the hypothesis that raising the intracellular ascorbate concentration protects the endothelial barrier from septic insult by inhibiting protein phosphatase type 2A. Monolayer cultures of microvascular endothelial cells were incubated with ascorbate, dehydroascorbic acid (DHAA), the NADPH oxidase inhibitors apocynin and diphenyliodonium, or the PP2A inhibitor okadaic acid and then were exposed to septic insult (lipopolysaccharide and interferon-gamma). Under standard culture conditions that depleted intracellular ascorbate, septic insult stimulated oxidant production and PP2A activity, dephosphorylated phosphoserine and phosphothreonine residues in the tight junction-associated protein occludin, decreased the abundance of occludin at cell borders, and increased monolayer permeability to albumin. NADPH oxidase inhibitors prevented PP2A activation and monolayer leak, showing that these changes required reactive oxygen species. Okadaic acid, at a concentration that inhibited PP2A activity and monolayer leak, prevented occludin dephosphorylation and redistribution, implicating PP2A in the response of occludin to septic insult. Incubation with ascorbate or DHAA raised intracellular ascorbate concentrations and mitigated the effects of septic insult. In conclusion, ascorbate acts within microvascular endothelial cells to inhibit septic stimulation of oxidant production by NADPH oxidase and thereby prevents PP2A activation, PP2A-dependent dephosphorylation and redistribution of occludin, and disruption of the endothelial barrier.

Keywords: Animals
Antioxidants / pharmacology
Ascorbic Acid / pharmacology*
Cells, Cultured
Endothelial Cells / drug effects*
Endothelial Cells / metabolism
Membrane Proteins / metabolism
Microvessels / cytology
Protein Phosphatase 2 / antagonists & inhibitors*
Protein Phosphatase 2 / metabolism
Sepsis / metabolism*