Divergent roles of endothelial NF-kappa B in multiple organ injury and bacterial clearance in mouse models of sepsis

作者：Ye Xiaobing; Ding Jianqiang; Zhou Xiaozhou; Chen Guoqian; Liu Shu Fang^*

来源：Journal of Experimental Medicine, 2008, 205(6): 1303-1315.

DOI：10.1084/jem.20071393

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.

• 出版日期2008-6-9
• 单位河北医科大学