Intestinal barrier disruption has been implicated in several intestinal and systemic disorders including alcoholic liver disease (ALD). Using monolayers of intestinal (Caco-2) cells, we showed that ethanol (EtOH) disrupts the barrier integrity via destabilization of the cytoskeleton. Because proinflammatory conditions are associated with activation of NF-kappa B (NF-kappa B), we hypothesized that EtOH induces disruption of cytoskeletal assembly and barrier integrity by activating NF-kappa B. Parental cells were pretreated with pharmacological modulators of NF-kappa B. Other cells were stably transfected with a dominant negative mutant for the NF-kappa B inhibitor, I-kappa B alpha. Monolayers of each cell type were exposed to EtOH and we then monitored monolayer barrier integrity (permeability); cytoskeletal stability and molecular dynamics (confocal microscopy and irnmunoblotting); intracellular levels of the I-kappa B alpha (immunoblotting); subcellular distribution and activity of NF-kappa B (immunoblotting and sensitive ELISA); and intracellular alterations in the 43 kDa protein of the actin cytoskeleton, polymerized F-actin, and monomeric G-actin (SDS-PAGE fractionation). EtOH caused destabilizing alterations, including I-kappa B alpha. degradation, NF-kappa B nuclear translocation, NF-kappa B subunit (p50 and p65) activation, actin disassembly (up arrow G-, down arrow F-), actin cytoskeleton instability, and barrier disruption. Inhibitors of NF-kappa B and stabilizersof I-kappa B alpha(e.g.,MG-132, lactacystin,etc) prevented NF-kappa B activation while protecting against EtOH-induced injury. In transfected I-kappa B alpha mutant clones, stabilization Of I-kappa B alpha to inactivate NF-kappa B protected against all measures of EtOH-induced injury. Our data support several novel mechanisms where NF-kappa B can affect the molecular dynamics of the F-actin cytoskeleton and intestinal barrier integrity under conditions of EtOH injury. (1) EtOH induces disruption of the F-actin cytoskeleton and of intestinal barrier integrity, in part, through I-kappa B alpha degradation and NF-kappa B activation; (2) The mechanism underlying this pathophysiological effect of the NF-kappa B appears to involve instability of the assembly of the subunit components of actin network. (c) 2007 Elsevier Inc. All rights reserved.