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Loss of Claudin-3 Impairs Hepatic Metabolism, Biliary Barrier Function, and Cell Proliferation in the Murine Liver

BACKGROUND & AIMS: Tight junctions in the liver are essential to maintain the blood-biliary barrier, however, the functional contribution of individual tight junction proteins to barrier and metabolic homeostasis remains largely unexplored. Here, we describe the cell type–specific expression of...

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Autores principales: Baier, Felix Alexander, Sánchez-Taltavull, Daniel, Yarahmadov, Tural, Castellà, Cristina Gómez, Jebbawi, Fadi, Keogh, Adrian, Tombolini, Riccardo, Odriozola, Adolfo, Dias, Mariana Castro, Deutsch, Urban, Furuse, Mikio, Engelhardt, Britta, Zuber, Benoît, Odermatt, Alex, Candinas, Daniel, Stroka, Deborah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8273426/
https://www.ncbi.nlm.nih.gov/pubmed/33866021
http://dx.doi.org/10.1016/j.jcmgh.2021.04.003
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author Baier, Felix Alexander
Sánchez-Taltavull, Daniel
Yarahmadov, Tural
Castellà, Cristina Gómez
Jebbawi, Fadi
Keogh, Adrian
Tombolini, Riccardo
Odriozola, Adolfo
Dias, Mariana Castro
Deutsch, Urban
Furuse, Mikio
Engelhardt, Britta
Zuber, Benoît
Odermatt, Alex
Candinas, Daniel
Stroka, Deborah
author_facet Baier, Felix Alexander
Sánchez-Taltavull, Daniel
Yarahmadov, Tural
Castellà, Cristina Gómez
Jebbawi, Fadi
Keogh, Adrian
Tombolini, Riccardo
Odriozola, Adolfo
Dias, Mariana Castro
Deutsch, Urban
Furuse, Mikio
Engelhardt, Britta
Zuber, Benoît
Odermatt, Alex
Candinas, Daniel
Stroka, Deborah
author_sort Baier, Felix Alexander
collection PubMed
description BACKGROUND & AIMS: Tight junctions in the liver are essential to maintain the blood-biliary barrier, however, the functional contribution of individual tight junction proteins to barrier and metabolic homeostasis remains largely unexplored. Here, we describe the cell type–specific expression of tight junction genes in the murine liver, and explore the regulation and functional importance of the transmembrane protein claudin-3 in liver metabolism, barrier function, and cell proliferation. METHODS: The cell type–specific expression of hepatic tight junction genes is described using our mouse liver single-cell sequencing data set. Differential gene expression in Cldn3(-/-) and Cldn3(+/+) livers was assessed in young and aged mice by RNA sequencing (RNA-seq), and hepatic tissue was analyzed for lipid content and bile acid composition. A surgical model of partial hepatectomy was used to induce liver cell proliferation. RESULTS: Claudin-3 is a highly expressed tight junction protein found in the liver and is expressed predominantly in hepatocytes and cholangiocytes. The histology of Cldn3(-/-) livers showed no overt phenotype, and the canalicular tight junctions appeared intact. Nevertheless, by RNA-seq we detected a down-regulation of metabolic pathways in the livers of Cldn3(-/-) young and aged mice, as well as a decrease in lipid content and a weakened biliary barrier for primary bile acids, such as taurocholic acid, taurochenodeoxycholic acid, and taurine-conjugated muricholic acid. Coinciding with defects in the biliary barrier and lower lipid metabolism, there was a diminished hepatocyte proliferative response in Cldn3(-/-) mice after partial hepatectomy. CONCLUSIONS: Our data show that, in the liver, claudin-3 is necessary to maintain metabolic homeostasis, retention of bile acids, and optimal hepatocyte proliferation during liver regeneration. The RNA-seq data set can be accessed at: https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE159914.
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spelling pubmed-82734262021-07-19 Loss of Claudin-3 Impairs Hepatic Metabolism, Biliary Barrier Function, and Cell Proliferation in the Murine Liver Baier, Felix Alexander Sánchez-Taltavull, Daniel Yarahmadov, Tural Castellà, Cristina Gómez Jebbawi, Fadi Keogh, Adrian Tombolini, Riccardo Odriozola, Adolfo Dias, Mariana Castro Deutsch, Urban Furuse, Mikio Engelhardt, Britta Zuber, Benoît Odermatt, Alex Candinas, Daniel Stroka, Deborah Cell Mol Gastroenterol Hepatol Original Research BACKGROUND & AIMS: Tight junctions in the liver are essential to maintain the blood-biliary barrier, however, the functional contribution of individual tight junction proteins to barrier and metabolic homeostasis remains largely unexplored. Here, we describe the cell type–specific expression of tight junction genes in the murine liver, and explore the regulation and functional importance of the transmembrane protein claudin-3 in liver metabolism, barrier function, and cell proliferation. METHODS: The cell type–specific expression of hepatic tight junction genes is described using our mouse liver single-cell sequencing data set. Differential gene expression in Cldn3(-/-) and Cldn3(+/+) livers was assessed in young and aged mice by RNA sequencing (RNA-seq), and hepatic tissue was analyzed for lipid content and bile acid composition. A surgical model of partial hepatectomy was used to induce liver cell proliferation. RESULTS: Claudin-3 is a highly expressed tight junction protein found in the liver and is expressed predominantly in hepatocytes and cholangiocytes. The histology of Cldn3(-/-) livers showed no overt phenotype, and the canalicular tight junctions appeared intact. Nevertheless, by RNA-seq we detected a down-regulation of metabolic pathways in the livers of Cldn3(-/-) young and aged mice, as well as a decrease in lipid content and a weakened biliary barrier for primary bile acids, such as taurocholic acid, taurochenodeoxycholic acid, and taurine-conjugated muricholic acid. Coinciding with defects in the biliary barrier and lower lipid metabolism, there was a diminished hepatocyte proliferative response in Cldn3(-/-) mice after partial hepatectomy. CONCLUSIONS: Our data show that, in the liver, claudin-3 is necessary to maintain metabolic homeostasis, retention of bile acids, and optimal hepatocyte proliferation during liver regeneration. The RNA-seq data set can be accessed at: https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE159914. Elsevier 2021-04-15 /pmc/articles/PMC8273426/ /pubmed/33866021 http://dx.doi.org/10.1016/j.jcmgh.2021.04.003 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Research
Baier, Felix Alexander
Sánchez-Taltavull, Daniel
Yarahmadov, Tural
Castellà, Cristina Gómez
Jebbawi, Fadi
Keogh, Adrian
Tombolini, Riccardo
Odriozola, Adolfo
Dias, Mariana Castro
Deutsch, Urban
Furuse, Mikio
Engelhardt, Britta
Zuber, Benoît
Odermatt, Alex
Candinas, Daniel
Stroka, Deborah
Loss of Claudin-3 Impairs Hepatic Metabolism, Biliary Barrier Function, and Cell Proliferation in the Murine Liver
title Loss of Claudin-3 Impairs Hepatic Metabolism, Biliary Barrier Function, and Cell Proliferation in the Murine Liver
title_full Loss of Claudin-3 Impairs Hepatic Metabolism, Biliary Barrier Function, and Cell Proliferation in the Murine Liver
title_fullStr Loss of Claudin-3 Impairs Hepatic Metabolism, Biliary Barrier Function, and Cell Proliferation in the Murine Liver
title_full_unstemmed Loss of Claudin-3 Impairs Hepatic Metabolism, Biliary Barrier Function, and Cell Proliferation in the Murine Liver
title_short Loss of Claudin-3 Impairs Hepatic Metabolism, Biliary Barrier Function, and Cell Proliferation in the Murine Liver
title_sort loss of claudin-3 impairs hepatic metabolism, biliary barrier function, and cell proliferation in the murine liver
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8273426/
https://www.ncbi.nlm.nih.gov/pubmed/33866021
http://dx.doi.org/10.1016/j.jcmgh.2021.04.003
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