Journal
CRITICAL CARE MEDICINE
Volume 37, Issue 5, Pages 1729-1734Publisher
LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/CCM.0b013e31819dee81
Keywords
signal transducer and activator of transcription-3; liver; animal models; janus kinase; signal transduction; cytokines
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Funding
- NIGMS [5R01 GM059930-08, 5T32GM007612-30]
- Stavropoulos Sepsis Research Program
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Objective: Sepsis impairs the activation of the interleukin (IL)-6 dependent transcription factor signal transducer and activator of transcription (STAT)-3. However, the molecular basis for depressed functionality has not been characterized. In this study, we test the hypothesis that altered signal transduction results from a change in the activation state of one or more of the components of the intracellular IL-6-linked pathway. Design: Randomized prospective experimental study. Setting: University medical laboratory. Subjects: Male, 6-8-week-old C57/BI6 mice. Interventions: Cecal ligation and single puncture (CLP) or cecal ligation and double puncture (2CLP) was used to model mild and fulminant sepsis, respectively. Sham-operated and unoperated animals served as controls. All animals were fluid resuscitated at the time of surgery and every 24 hours thereafter. Surviving animals were euthanized at 3, 6, 16, 24, 48, and 72 hours; blood samples were obtained and liver tissue was harvested. Measurements and Main Results: Serum IL-6 levels were elevated in both CLP and 2CLP relative to controls. STAT-3 DNA binding activity and nuclear phosphorylated-STAT-3 levels were elevated in CLP but decreased abruptly 24 hours after 2CLP. This 2CLP-induced alteration was associated with attenuated phosphorylation of the key transcellular glycoprotein (gp) 130. Abundance and phosphorylation of the other key component of IL-6 signal transduction pathway, janus kinase-1, was unchanged following either CLP or 2CLP. 2CLP also did not cause disassociation of the gp130-janus kinase-1 complex. Conclusions: Impaired gp130 phosphorylation may be responsible for IL-6 hyporesponsiveness during sepsis. (Crit Care Med 2009; 37:1729-1734)
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