Hepatocyte apoptosis is tumor promoting in murine nonalcoholic steatohepatitis
Jazyk angličtina Země Velká Británie, Anglie Médium electronic
Typ dokumentu časopisecké články, Research Support, N.I.H., Extramural, práce podpořená grantem
Grantová podpora
P30 DK084567
NIDDK NIH HHS - United States
R01 DK041876
NIDDK NIH HHS - United States
PubMed
32015322
PubMed Central
PMC6997423
DOI
10.1038/s41419-020-2283-9
PII: 10.1038/s41419-020-2283-9
Knihovny.cz E-zdroje
- MeSH
- apoptóza * MeSH
- dieta škodlivé účinky MeSH
- hepatitida patologie MeSH
- hepatocyty metabolismus patologie MeSH
- jaterní cirhóza patologie MeSH
- játra zranění patologie MeSH
- karcinogeneze * MeSH
- modely nemocí na zvířatech MeSH
- myši inbrední C57BL MeSH
- myši knockoutované MeSH
- myši MeSH
- nádory jater patologie MeSH
- nealkoholová steatóza jater etiologie patologie MeSH
- obezita etiologie patologie MeSH
- proliferace buněk MeSH
- protein MCL-1 nedostatek MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Research Support, N.I.H., Extramural MeSH
- Názvy látek
- Mcl1 protein, mouse MeSH Prohlížeč
- protein MCL-1 MeSH
Nonalcoholic fatty liver disease is the most common chronic liver disease and may progress to nonalcoholic steatohepatitis (NASH) and hepatocellular carcinoma (HCC). The molecular determinants of this pathogenic progression, however, remain largely undefined. Since liver tumorigenesis is driven by apoptosis, we examined the effect of overt hepatocyte apoptosis in a mouse model of NASH using mice lacking myeloid cell leukemia 1 (Mcl1), a pro-survival member of the BCL-2 protein family. Hepatocyte-specific Mcl1 knockout (Mcl1∆hep) mice and control littermates were fed chow or FFC (high saturated fat, fructose, and cholesterol) diet, which induces NASH, for 4 and 10 months. Thereafter, liver injury, inflammation, fibrosis, and tumor development were evaluated biochemically and histologically. Mcl1∆hep mice fed with the FFC diet for 4 months displayed a marked increase in liver injury, hepatocyte apoptosis, hepatocyte proliferation, macrophage-associated liver inflammation, and pericellular fibrosis in contrast to chow-fed Mcl1∆hep and FFC diet-fed Mcl1-expressing littermates. After 10 months of feeding, 78% of FFC diet-fed Mcl1∆hep mice developed liver tumors compared to 38% of chow-fed mice of the same genotype. Tumors in FFC diet-fed Mcl1∆hep mice were characterized by cytologic atypia, altered liver architecture, immunopositivity for glutamine synthetase, and histologically qualified as HCC. In conclusion, this study provides evidence that excessive hepatocyte apoptosis exacerbates the NASH phenotype with enhancement of tumorigenesis in mice.
Department of Chemistry and Biochemistry Mendel University in Brno Brno Czech Republic
Division of Chronic Inflammation and Cancer German Cancer Research Center Heidelberg Germany
Division of Gastroenterology and Hepatology Mayo Clinic Rochester MN USA
Institute of Molecular Cancer Research University Zurich Zurich Switzerland
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