Journal
JOURNAL OF EXPERIMENTAL MEDICINE
Volume 205, Issue 6, Pages 1303-1315Publisher
ROCKEFELLER UNIV PRESS
DOI: 10.1084/jem.20071393
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- PHS HHS [NIGMS 063907] Funding Source: Medline
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To define the roles of endothelial-intrinsic nuclear factor kappa B (NF-kappa B) activity in host defense and multiple organ injury in response to sepsis, we generated double transgenic (TG) mice (EC-rtTA/I-kappa B alpha mt) that conditionally overexpress a degradation-resistant form of the NF-kappa B inhibitor I-kappa B alpha (I-kappa B alpha mt) selectively on vascular endothelium. The EC-rtTA/I-kappa B alpha mt mice had no basal, but a relatively high level of doxycycline-inducible, I-kappa B alpha mt expression. I-kappa B alpha mt expression was detected in endothelial cells, but not in fibroblasts, macrophages, and whole blood cells, confirming that transgene expression was restricted to the endothelium. When subjected to endotoxemia, EC-rtTA/I-kappa B alpha mt mice showed endothelial-selective blockade of NF-kappa B activation, repressed expression of multiple endothelial adhesion molecules, reduced neutrophil infiltration into multiple organs, decreased endothelial permeability, ameliorated multiple organ injury, reduced systemic hypotension, and abrogated intravascular coagulation. When subjected to cecal ligation and puncture-induced sepsis, the TG mice had less severe multiple organ injury and improved survival compared with wild-type (WT) mice. WT and EC-rtTA/I-kappa B alpha mt mice had comparable capacity to clear three different pathogenic bacteria. Our data demonstrate that endothelial NF-kappa B activity is an essential mediator of septic multiple organ inflammation and injury but plays little role in the host defense response to eradicate invading pathogenic bacteria.
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