Research Article

Human Neutrophil Defensins Disrupt Liver Interendothelial Junctions and Aggravate Sepsis

Figure 7

Genetic deficiency of NLRP3 or caspase-1 abrogated the damaging effects caused by high dose of HNP-1 during sepsis progression. Nlrp3-/- mice and Casp1-/- mice were intraperitoneally administered a high dose of HNP-1 (10 mg/kg body weight), a low dose of HNP-1 (0.5 mg/kg body weight), or PBS 6 hours after CLP. (a, b) Survival of Nlrp3-/- mice (a) and Casp1-/- mice (b) over time was monitored. In (a), mice for the high-dose group, and mice for the low-dose group and for the PBS group. In (b), mice for each group. (c, d) Representative images (c) and comparisons of VE-cadherin abundance (d) in the liver of Casp1-/- mice administered a high dose of HNP-1 or PBS at 48 hours after CLP is shown. The results presented are the of 3 mice in each group. Scale bars, 50 μm.
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