Reference : Resistance of collagenase-2 (MMP-8) deficient mice to TNF-induced lethal hepatitis
Scientific journals : Article
Life sciences : Biochemistry, biophysics & molecular biology
http://hdl.handle.net/2268/33215
Resistance of collagenase-2 (MMP-8) deficient mice to TNF-induced lethal hepatitis
English
Van Lint, Ph [ > > ]
Wielockx, B. [ > > ]
Puimege, L. [ > > ]
Noël, Agnès mailto [Université de Liège - ULg > Département des sciences biomédicales et précliniques > Biologie cellulaire et moléculaire appliquée à l'homme >]
Lopez-Otin, C. [ > > ]
Libert, C. [ > > ]
2005
Journal of Immunology
American Association of Immunologists
175
11
7642-9
Yes (verified by ORBi)
International
0022-1767
1550-6606
Baltimore
MD
[en] Acute fulminant liver failure is a serious worldwide health problem. Despite maximal supportive intensive care treatment, the disease offers a poor prognosis, with mortality rates of >80%. We have previously shown that a broad-spectrum inhibitor of matrix metalloproteinases (MMPs) confers complete protection in a mouse model of TNF-induced lethal hepatitis, thereby suggesting the possibility of protecting cancer patients against the deleterious side effects of TNF therapy. In our search for the individual matrix metalloproteinases involved, we found that the recently generated MMP-8-deficient mice are significantly protected against TNF-induced acute hepatitis. In contrast to their wild-type counterparts, MMP-8-null mice display very little hepatocyte necrosis and apoptosis, resulting in a much better survival outcome. We found that these animals clearly display impaired leukocyte influx into the liver and no release of the neutrophil-specific, LPS-induced CXC chemokine. Our findings provide evidence that MMP-8 plays an essential role in acute liver failure and might be a promising new target for the treatment for this illness.
http://hdl.handle.net/2268/33215

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