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SHR Neuro Krebs Kardio Lipid Stoffw Microb

Loebermann, M; Sombetzki, M; Langner, C; Fuchsbichler, A; Gumhold, J; Silbert, D; Riebold, D; Holtfreter, M; Fickert, P; Nizze, H; Trauner, M; Reisinger, EC.
Imbalance of pro- and antifibrogenic genes and bile duct injury in murine Schistosoma mansoni infection-induced liver fibrosis.
Trop Med Int Health. 2009; 14(11):1418-1425 Doi: 10.1111/j.1365-3156.2009.02387.x [OPEN ACCESS]
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Co-Autor*innen der Med Uni Graz
Fickert Peter
Langner Cord
Silbert-Wagner Dagmar
Sommer Judith
Trauner Michael
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Abstract:
The murine model of Schistosoma mansoni infection is characterized by strong fibrosis and little hepatocellular injury. The objective of this study was to evaluate the potential link between hepatic schistosomiasis and bile duct injury in relation to the expression of profibrotic cytokines and fibrosis-related genes. Hepatic schistosomiasis was induced via percutaneous infection of mice with 50 S. mansoni cercariae. Markers of fibrosis including matrixmetalloproteinases (MMPs) and tissue-inhibitors of metalloproteinases (TIMPs), as well as markers of bile duct injury (keratin-19, VCAM-1) were studied during 24 weeks after infection by RT-PCR and immunohistochemistry. Liver biochemistry revealed no differences in serum transaminase and alkaline phosphatase levels in infected and uninfected mice. Total liver hydroxyproline content was increased 5-fold (P < 0.05) after infection. Gene expression analysis revealed MMP-2 (12-fold, P < 0.05) and TIMP-1 (48-fold, P < 0.05) up-regulation after infection. The balance of MMP and TIMP was shifted towards TIMP. Bile ducts were engulfed by adjacent granulomas resulting in ductular proliferation (keratin-19). VCAM-1 expression and inflammatory infiltrates were reduced. This study demonstrates that schistosomiasis is associated with (i) an imbalance of MMP-2 and TIMP-1 as key players of fibrogenesis and (ii) with secondary bile duct alterations leading to ductular proliferation possibly contributing to fibrosis.
Find related publications in this database (using NLM MeSH Indexing)
Alkaline Phosphatase - metabolism
Animals -
Bile Duct Diseases - metabolism
Biological Markers - metabolism
Cytokines - metabolism
Keratin-19 - metabolism
Liver Cirrhosis - enzymology Liver Cirrhosis - genetics
Metalloproteases - analysis Metalloproteases - metabolism
Mice -
Models, Animal -
Reverse Transcriptase Polymerase Chain Reaction -
Schistosoma mansoni - genetics
Schistosomiasis mansoni - genetics
Tissue Inhibitor of Metalloproteinases - analysis Tissue Inhibitor of Metalloproteinases - genetics
Transaminases - metabolism
Vascular Cell Adhesion Molecule-1 - genetics

Find related publications in this database (Keywords)
bile duct
fibrosis
liver
injury
schistosomiasis
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