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FGF19 Regulates Cell Proliferation, Glucose and Bile Acid Metabolism via FGFR4-Dependent and Independent Pathways

Fibroblast growth factor 19 (FGF19) is a hormone-like protein that regulates carbohydrate, lipid and bile acid metabolism. At supra-physiological doses, FGF19 also increases hepatocyte proliferation and induces hepatocellular carcinogenesis in mice. Much of FGF19 activity is attributed to the activa...

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Autores principales: Wu, Ai-Luen, Coulter, Sally, Liddle, Christopher, Wong, Anne, Eastham-Anderson, Jeffrey, French, Dorothy M., Peterson, Andrew S., Sonoda, Junichiro
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3060878/
https://www.ncbi.nlm.nih.gov/pubmed/21437243
http://dx.doi.org/10.1371/journal.pone.0017868
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author Wu, Ai-Luen
Coulter, Sally
Liddle, Christopher
Wong, Anne
Eastham-Anderson, Jeffrey
French, Dorothy M.
Peterson, Andrew S.
Sonoda, Junichiro
author_facet Wu, Ai-Luen
Coulter, Sally
Liddle, Christopher
Wong, Anne
Eastham-Anderson, Jeffrey
French, Dorothy M.
Peterson, Andrew S.
Sonoda, Junichiro
author_sort Wu, Ai-Luen
collection PubMed
description Fibroblast growth factor 19 (FGF19) is a hormone-like protein that regulates carbohydrate, lipid and bile acid metabolism. At supra-physiological doses, FGF19 also increases hepatocyte proliferation and induces hepatocellular carcinogenesis in mice. Much of FGF19 activity is attributed to the activation of the liver enriched FGF Receptor 4 (FGFR4), although FGF19 can activate other FGFRs in vitro in the presence of the coreceptor βKlotho (KLB). In this report, we investigate the role of FGFR4 in mediating FGF19 activity by using Fgfr4 deficient mice as well as a variant of FGF19 protein (FGF19v) which is specifically impaired in activating FGFR4. Our results demonstrate that FGFR4 activation mediates the induction of hepatocyte proliferation and the suppression of bile acid biosynthesis by FGF19, but is not essential for FGF19 to improve glucose and lipid metabolism in high fat diet fed mice as well as in leptin-deficient ob/ob mice. Thus, FGF19 acts through multiple receptor pathways to elicit pleiotropic effects in regulating nutrient metabolism and cell proliferation.
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spelling pubmed-30608782011-03-23 FGF19 Regulates Cell Proliferation, Glucose and Bile Acid Metabolism via FGFR4-Dependent and Independent Pathways Wu, Ai-Luen Coulter, Sally Liddle, Christopher Wong, Anne Eastham-Anderson, Jeffrey French, Dorothy M. Peterson, Andrew S. Sonoda, Junichiro PLoS One Research Article Fibroblast growth factor 19 (FGF19) is a hormone-like protein that regulates carbohydrate, lipid and bile acid metabolism. At supra-physiological doses, FGF19 also increases hepatocyte proliferation and induces hepatocellular carcinogenesis in mice. Much of FGF19 activity is attributed to the activation of the liver enriched FGF Receptor 4 (FGFR4), although FGF19 can activate other FGFRs in vitro in the presence of the coreceptor βKlotho (KLB). In this report, we investigate the role of FGFR4 in mediating FGF19 activity by using Fgfr4 deficient mice as well as a variant of FGF19 protein (FGF19v) which is specifically impaired in activating FGFR4. Our results demonstrate that FGFR4 activation mediates the induction of hepatocyte proliferation and the suppression of bile acid biosynthesis by FGF19, but is not essential for FGF19 to improve glucose and lipid metabolism in high fat diet fed mice as well as in leptin-deficient ob/ob mice. Thus, FGF19 acts through multiple receptor pathways to elicit pleiotropic effects in regulating nutrient metabolism and cell proliferation. Public Library of Science 2011-03-18 /pmc/articles/PMC3060878/ /pubmed/21437243 http://dx.doi.org/10.1371/journal.pone.0017868 Text en Wu et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Wu, Ai-Luen
Coulter, Sally
Liddle, Christopher
Wong, Anne
Eastham-Anderson, Jeffrey
French, Dorothy M.
Peterson, Andrew S.
Sonoda, Junichiro
FGF19 Regulates Cell Proliferation, Glucose and Bile Acid Metabolism via FGFR4-Dependent and Independent Pathways
title FGF19 Regulates Cell Proliferation, Glucose and Bile Acid Metabolism via FGFR4-Dependent and Independent Pathways
title_full FGF19 Regulates Cell Proliferation, Glucose and Bile Acid Metabolism via FGFR4-Dependent and Independent Pathways
title_fullStr FGF19 Regulates Cell Proliferation, Glucose and Bile Acid Metabolism via FGFR4-Dependent and Independent Pathways
title_full_unstemmed FGF19 Regulates Cell Proliferation, Glucose and Bile Acid Metabolism via FGFR4-Dependent and Independent Pathways
title_short FGF19 Regulates Cell Proliferation, Glucose and Bile Acid Metabolism via FGFR4-Dependent and Independent Pathways
title_sort fgf19 regulates cell proliferation, glucose and bile acid metabolism via fgfr4-dependent and independent pathways
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3060878/
https://www.ncbi.nlm.nih.gov/pubmed/21437243
http://dx.doi.org/10.1371/journal.pone.0017868
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