Abstract | BACKGROUND & AIMS:
Keratins (Ks) 7, 8, 18 and 19 constitute important markers and modifiers of liver disease. In mice, K8 and K18 are stress inducible and a dysregulated K8 > K18 stoichiometry predisposes to formation of Mallory-Denk bodies (MDBs), i.e. aggregates characteristic of chronic liver disorders such as alcoholic liver disease (ALD). In our study, we analyse the expression and the regulation of keratins in context of human liver disease. METHODS: RESULTS: K7, K8 and K18 were 1.5- to 3-fold upregulated in livers of ALD and HCV patients with a more active disease, but not in HBV/NASH subjects, while K19 was significantly elevated in all analysed disorders. K8 and K18 expression displayed a strong correlation (r = 0.89), but dysregulated levels with the K8 > K18 state were seen in ALD. All keratins were overexpressed in subjects with moderate vs. minimal inflammation, while K7, K8 and K18 were upregulated in patients with advanced liver fibrosis. In HepG2/Hep3B cells, IL-6 treatment but not IL-1β or TNF-α significantly increased K8 and K18 expression and elevated K18 levels were seen after turpentine injection. CONCLUSIONS:
Keratins represent type II acute-phase responsive genes overexpressed in specific human liver disorders. A K8 > K18 state occurs in ALD and predisposes to MDB formation.
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Authors | Nurdan Guldiken, Valentyn Usachov, Kateryna Levada, Christian Trautwein, Marianne Ziol, Pierre Nahon, Pavel Strnad |
Journal | Liver international : official journal of the International Association for the Study of the Liver
(Liver Int)
Vol. 35
Issue 4
Pg. 1203-12
(Apr 2015)
ISSN: 1478-3231 [Electronic] United States |
PMID | 24930437
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | © 2014 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd. |
Chemical References |
- Acute-Phase Proteins
- Inflammation Mediators
- KRT18 protein, human
- KRT8 protein, human
- Keratin-18
- Keratin-8
- Krt8 protein, mouse
- RNA, Messenger
- Turpentine
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Topics |
- Acute-Phase Proteins
(genetics)
- Adult
- Aged
- Animals
- Case-Control Studies
- Chemical and Drug Induced Liver Injury
(genetics)
- Disease Models, Animal
- Female
- Hep G2 Cells
- Hepatitis B, Chronic
(genetics)
- Hepatitis C, Chronic
(genetics)
- Humans
- Inflammation Mediators
(metabolism)
- Keratin-18
(genetics)
- Keratin-8
(genetics)
- Liver
(metabolism)
- Liver Diseases
(diagnosis, genetics, metabolism)
- Liver Diseases, Alcoholic
(genetics)
- Male
- Mice, Inbred C57BL
- Middle Aged
- Non-alcoholic Fatty Liver Disease
(genetics)
- RNA, Messenger
(metabolism)
- Turpentine
- Up-Regulation
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