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Caveolin-1 Impacts on TGF-β Regulation of Metabolic Gene Signatures in Hepatocytes

Caveolin-1 (CAV1) is a membrane protein associated with metabolism in various cell types. The transforming growth factor beta (TGF-β) is a pro-fibrogenic cytokine in the liver, but its metabolic gene signatures remain unclear to date. We have previously shown that CAV1 alters TGF-β signaling and blo...

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Autores principales: Han, Mei, Nwosu, Zeribe Chike, Piorońska, Weronika, Ebert, Matthias Philip, Dooley, Steven, Meyer, Christoph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7005071/
https://www.ncbi.nlm.nih.gov/pubmed/32082178
http://dx.doi.org/10.3389/fphys.2019.01606
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author Han, Mei
Nwosu, Zeribe Chike
Piorońska, Weronika
Ebert, Matthias Philip
Dooley, Steven
Meyer, Christoph
author_facet Han, Mei
Nwosu, Zeribe Chike
Piorońska, Weronika
Ebert, Matthias Philip
Dooley, Steven
Meyer, Christoph
author_sort Han, Mei
collection PubMed
description Caveolin-1 (CAV1) is a membrane protein associated with metabolism in various cell types. The transforming growth factor beta (TGF-β) is a pro-fibrogenic cytokine in the liver, but its metabolic gene signatures remain unclear to date. We have previously shown that CAV1 alters TGF-β signaling and blocks its pro-apoptotic function. Here, we defined TGF-β-induced metabolic gene signatures in hepatocytes and assessed whether CAV1 abundance affects TGF-β control of those metabolic genes. Microarray analyses of primary hepatocytes after TGF-β stimulation (48 h) showed differential expression of 4224 genes, of which 721 are metabolic genes (adjusted p < 0.001). Functional annotation analysis revealed that TGF-β mainly suppresses metabolic gene network, including genes involved in glutathione, cholesterol, fatty acid, and amino acid metabolism. TGF-β also upregulated several genes related to glycan metabolism and ion transport. In contrast to TGF-β effects, CAV1 knockdown triggered the upregulation of metabolic genes. Immortalized mouse hepatocytes (AML12 cells) were used to validate the gene changes induced by TGF-β stimulation and CAV1 knockdown. Noteworthy, of the TGF-β metabolic target genes, CAV1 modulated the expression of 228 (27%). In conclusion, we present several novel metabolic gene signatures of TGF-β in hepatocytes and show that CAV1 abundance alters almost a third of these genes. These findings could enable a better understanding of TGF-β function in normal and diseased liver especially where differential CAV1 level is implicated.
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spelling pubmed-70050712020-02-20 Caveolin-1 Impacts on TGF-β Regulation of Metabolic Gene Signatures in Hepatocytes Han, Mei Nwosu, Zeribe Chike Piorońska, Weronika Ebert, Matthias Philip Dooley, Steven Meyer, Christoph Front Physiol Physiology Caveolin-1 (CAV1) is a membrane protein associated with metabolism in various cell types. The transforming growth factor beta (TGF-β) is a pro-fibrogenic cytokine in the liver, but its metabolic gene signatures remain unclear to date. We have previously shown that CAV1 alters TGF-β signaling and blocks its pro-apoptotic function. Here, we defined TGF-β-induced metabolic gene signatures in hepatocytes and assessed whether CAV1 abundance affects TGF-β control of those metabolic genes. Microarray analyses of primary hepatocytes after TGF-β stimulation (48 h) showed differential expression of 4224 genes, of which 721 are metabolic genes (adjusted p < 0.001). Functional annotation analysis revealed that TGF-β mainly suppresses metabolic gene network, including genes involved in glutathione, cholesterol, fatty acid, and amino acid metabolism. TGF-β also upregulated several genes related to glycan metabolism and ion transport. In contrast to TGF-β effects, CAV1 knockdown triggered the upregulation of metabolic genes. Immortalized mouse hepatocytes (AML12 cells) were used to validate the gene changes induced by TGF-β stimulation and CAV1 knockdown. Noteworthy, of the TGF-β metabolic target genes, CAV1 modulated the expression of 228 (27%). In conclusion, we present several novel metabolic gene signatures of TGF-β in hepatocytes and show that CAV1 abundance alters almost a third of these genes. These findings could enable a better understanding of TGF-β function in normal and diseased liver especially where differential CAV1 level is implicated. Frontiers Media S.A. 2020-01-31 /pmc/articles/PMC7005071/ /pubmed/32082178 http://dx.doi.org/10.3389/fphys.2019.01606 Text en Copyright © 2020 Han, Nwosu, Piorońska, Ebert, Dooley and Meyer. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Han, Mei
Nwosu, Zeribe Chike
Piorońska, Weronika
Ebert, Matthias Philip
Dooley, Steven
Meyer, Christoph
Caveolin-1 Impacts on TGF-β Regulation of Metabolic Gene Signatures in Hepatocytes
title Caveolin-1 Impacts on TGF-β Regulation of Metabolic Gene Signatures in Hepatocytes
title_full Caveolin-1 Impacts on TGF-β Regulation of Metabolic Gene Signatures in Hepatocytes
title_fullStr Caveolin-1 Impacts on TGF-β Regulation of Metabolic Gene Signatures in Hepatocytes
title_full_unstemmed Caveolin-1 Impacts on TGF-β Regulation of Metabolic Gene Signatures in Hepatocytes
title_short Caveolin-1 Impacts on TGF-β Regulation of Metabolic Gene Signatures in Hepatocytes
title_sort caveolin-1 impacts on tgf-β regulation of metabolic gene signatures in hepatocytes
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7005071/
https://www.ncbi.nlm.nih.gov/pubmed/32082178
http://dx.doi.org/10.3389/fphys.2019.01606
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