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GDF11 induces mild hepatic fibrosis independent of metabolic health
J. Frohlich, K. Kovacovicova, T. Mazza, MR. Emma, D. Cabibi, M. Foti, C. Sobolewski, JA. Oben, M. Peyrou, F. Villarroya, M. Soresi, R. Rezzani, M. Cervello, F. Bonomini, A. Alisi, M. Vinciguerra
Language English Country United States
Document type Journal Article, Research Support, Non-U.S. Gov't
NLK
Free Medical Journals
from 2009
Freely Accessible Science Journals
from 2009-01-01
PubMed Central
from 2009
Europe PubMed Central
from 2009
Open Access Digital Library
from 2009-01-01
PubMed
33126224
DOI
10.18632/aging.104182
Knihovny.cz E-resources
- MeSH
- Cell Line MeSH
- Adult MeSH
- Liver Cirrhosis, Experimental chemically induced metabolism pathology MeSH
- Liver Cirrhosis diagnosis etiology genetics metabolism MeSH
- Hepatic Stellate Cells metabolism pathology MeSH
- Liver metabolism pathology MeSH
- Bone Morphogenetic Proteins genetics metabolism toxicity MeSH
- Middle Aged MeSH
- Humans MeSH
- Obesity, Morbid complications diagnosis MeSH
- Mice, Inbred C57BL MeSH
- Non-alcoholic Fatty Liver Disease diagnosis etiology genetics metabolism MeSH
- Disease Progression MeSH
- Growth Differentiation Factors genetics metabolism toxicity MeSH
- Signal Transduction MeSH
- Case-Control Studies MeSH
- Animals MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
BACKGROUND & AIMS: Growth Differentiation Factor 11 (GDF11) is an anti-aging factor, yet its role in liver diseases is not established. We evaluated the role of GDF11 in healthy conditions and in the transition from non-alcoholic fatty liver disease (NAFLD) to non-alcoholic steatohepatitis (NASH). RESULTS: GDF11 mRNA levels positively correlated with NAFLD activity score and with CPT1, SREBP, PPARγ and Col1A1 mRNA levels, and associated to portal fibrosis, in morbidly obese patients with NAFLD/NASH. GDF11-treated mice showed mildly exacerbated hepatic collagen deposition, accompanied by weight loss and without changes in liver steatosis or inflammation. GDF11 triggered ALK5-dependent SMAD2/3 nuclear translocation and the pro-fibrogenic activation of HSC. CONCLUSIONS: GDF11 supplementation promotes mild liver fibrosis. Even considering its beneficial metabolic effects, caution should be taken when considering therapeutics that regulate GDF11. METHODS: We analyzed liver biopsies from a cohort of 33 morbidly obese adults with NAFLD/NASH. We determined the correlations in mRNA expression levels between GDF11 and genes involved in NAFLD-to-NASH progression and with pathological features. We also exposed wild type or obese mice with NAFLD to recombinant GDF11 by daily intra-peritoneal injection and monitor the hepatic pathological changes. Finally, we analyzed GDF11-activated signaling pathways in hepatic stellate cells (HSC).
Bioinformatics Unit IRCCS Casa Sollievo della Sofferenza San Giovanni Rotondo Italy
CIBER Fisiopatología de la Obesidad y Nutrición Barcelona Catalonia Spain
Institut de Recerca Hospital de la Santa Creu i Sant Pau Barcelona Catalonia Spain
Institute for Biomedical Research and Innovation National Research Council Palermo Italy
International Clinical Research Center St Anne's University Hospital Brno Czech Republic
References provided by Crossref.org
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- $a BACKGROUND & AIMS: Growth Differentiation Factor 11 (GDF11) is an anti-aging factor, yet its role in liver diseases is not established. We evaluated the role of GDF11 in healthy conditions and in the transition from non-alcoholic fatty liver disease (NAFLD) to non-alcoholic steatohepatitis (NASH). RESULTS: GDF11 mRNA levels positively correlated with NAFLD activity score and with CPT1, SREBP, PPARγ and Col1A1 mRNA levels, and associated to portal fibrosis, in morbidly obese patients with NAFLD/NASH. GDF11-treated mice showed mildly exacerbated hepatic collagen deposition, accompanied by weight loss and without changes in liver steatosis or inflammation. GDF11 triggered ALK5-dependent SMAD2/3 nuclear translocation and the pro-fibrogenic activation of HSC. CONCLUSIONS: GDF11 supplementation promotes mild liver fibrosis. Even considering its beneficial metabolic effects, caution should be taken when considering therapeutics that regulate GDF11. METHODS: We analyzed liver biopsies from a cohort of 33 morbidly obese adults with NAFLD/NASH. We determined the correlations in mRNA expression levels between GDF11 and genes involved in NAFLD-to-NASH progression and with pathological features. We also exposed wild type or obese mice with NAFLD to recombinant GDF11 by daily intra-peritoneal injection and monitor the hepatic pathological changes. Finally, we analyzed GDF11-activated signaling pathways in hepatic stellate cells (HSC).
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