4.8 Article

NF-κB activation, rather than TNF, mediates hepatic inflammation in a murine dietary model of steatohepatitis

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GASTROENTEROLOGY
卷 129, 期 5, 页码 1663-1674

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W B SAUNDERS CO-ELSEVIER INC
DOI: 10.1053/j.gastro.2005.09.004

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Background& Aims: We explored the roles of nuclear factor-kappa B (NF-kappa B) and tumor necrosis factor (TNF) alpha (TNF-alpha) as mediators of inflammation in a nutritional model of steatohepatitis. Methods: Wild-type (wt), TNF null (-/-), and TNF receptor (R)-1-/- mice were fed a methionine- and choline-deficient (MCD) diet for up to 5 weeks. Liver injury (serum alanine aminotransferase [ALT]), hepatic inflammation, triglycerides, and lipid peroxide levels were determined. Hepatic NF-kappa B activation and expression of TNF and intercellular adhesion molecule-1 (ICAM-1) were assayed. Results: Irrespective of genotype, MCD diet-fed mice developed hepatic lipid peroxidation and serum ALT elevation; at day 10, livers from wt, TNF-/-, and TNFR-1-/- mice showed equivalent steatohepatitis. NF-kappa B/DNA binding was enhanced in hepatic nuclear fractions from MCD diet-fed wt mice compared with dietary controls; there were corresponding increases of ICAM-1 and TNF messenger RNA (mRNA). Likewise, NF-kappa B activation and ICAM-1 expression were enhanced by MCD dietary feeding in TNF-/- and TNFR-1-/- mice compared with respective controls. To establish whether NF-kappa B is a primary mediator of inflammation in experimental steatohepatitis, we overexpressed a mutant, nondegradable I kappa B (mI kappa B), delivered by adenovirus in vivo. As expected, hepatic mI kappa B expression reduced NF-kappa B/DNA binding induced by MCD dietary feeding, with resultant abrogation of ICAM-1 and TNF synthesis. Such blockade of NF-kappa B transcriptional activation substantially protected against development of steatohepatitis, with significant reductions in liver injury and hepatic inflammation. Conclusions: In the MCD dietary model of steatohepatitis, NF-kappa B is activated early and is an important proinflammatory mediator of lesion development, but steatohepatitis occurs independently of TNF synthesis and TNFR-1 activation.

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