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Glucagon contributes to liver zonation

Liver zonation characterizes the separation of metabolic pathways along the lobules and is required for optimal function. Wnt/β-catenin signaling controls metabolic zonation by activating genes in the perivenous hepatocytes, while suppressing genes in the periportal counterparts. We now demonstrate...

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Autores principales: Cheng, Xiping, Kim, Sun Y., Okamoto, Haruka, Xin, Yurong, Yancopoulos, George D., Murphy, Andrew J., Gromada, Jesper
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5924920/
https://www.ncbi.nlm.nih.gov/pubmed/29555772
http://dx.doi.org/10.1073/pnas.1721403115
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author Cheng, Xiping
Kim, Sun Y.
Okamoto, Haruka
Xin, Yurong
Yancopoulos, George D.
Murphy, Andrew J.
Gromada, Jesper
author_facet Cheng, Xiping
Kim, Sun Y.
Okamoto, Haruka
Xin, Yurong
Yancopoulos, George D.
Murphy, Andrew J.
Gromada, Jesper
author_sort Cheng, Xiping
collection PubMed
description Liver zonation characterizes the separation of metabolic pathways along the lobules and is required for optimal function. Wnt/β-catenin signaling controls metabolic zonation by activating genes in the perivenous hepatocytes, while suppressing genes in the periportal counterparts. We now demonstrate that glucagon opposes the actions of Wnt/β-catenin signaling on gene expression and metabolic zonation pattern. The effects were more pronounced in the periportal hepatocytes where 28% of all genes were activated by glucagon and inhibited by Wnt/β-catenin. The glucagon and Wnt/β-catenin receptors and their signaling pathways are uniformly distributed in periportal and perivenous hepatocytes and the expression is not regulated by the opposing signal. Collectively, our results show that glucagon controls gene expression and metabolic zonation in the liver through a counterplay with the Wnt/β-catenin signaling pathway.
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spelling pubmed-59249202018-04-30 Glucagon contributes to liver zonation Cheng, Xiping Kim, Sun Y. Okamoto, Haruka Xin, Yurong Yancopoulos, George D. Murphy, Andrew J. Gromada, Jesper Proc Natl Acad Sci U S A PNAS Plus Liver zonation characterizes the separation of metabolic pathways along the lobules and is required for optimal function. Wnt/β-catenin signaling controls metabolic zonation by activating genes in the perivenous hepatocytes, while suppressing genes in the periportal counterparts. We now demonstrate that glucagon opposes the actions of Wnt/β-catenin signaling on gene expression and metabolic zonation pattern. The effects were more pronounced in the periportal hepatocytes where 28% of all genes were activated by glucagon and inhibited by Wnt/β-catenin. The glucagon and Wnt/β-catenin receptors and their signaling pathways are uniformly distributed in periportal and perivenous hepatocytes and the expression is not regulated by the opposing signal. Collectively, our results show that glucagon controls gene expression and metabolic zonation in the liver through a counterplay with the Wnt/β-catenin signaling pathway. National Academy of Sciences 2018-04-24 2018-03-19 /pmc/articles/PMC5924920/ /pubmed/29555772 http://dx.doi.org/10.1073/pnas.1721403115 Text en Copyright © 2018 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle PNAS Plus
Cheng, Xiping
Kim, Sun Y.
Okamoto, Haruka
Xin, Yurong
Yancopoulos, George D.
Murphy, Andrew J.
Gromada, Jesper
Glucagon contributes to liver zonation
title Glucagon contributes to liver zonation
title_full Glucagon contributes to liver zonation
title_fullStr Glucagon contributes to liver zonation
title_full_unstemmed Glucagon contributes to liver zonation
title_short Glucagon contributes to liver zonation
title_sort glucagon contributes to liver zonation
topic PNAS Plus
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5924920/
https://www.ncbi.nlm.nih.gov/pubmed/29555772
http://dx.doi.org/10.1073/pnas.1721403115
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