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Enhancement of hepatocyte differentiation from human embryonic stem cells by Chinese medicine Fuzhenghuayu

Chinese medicine, Fuzhenghuayu (FZHY), appears to prevent fibrosis progression and improve liver function in humans. Here we found that FZHY enhanced hepatocyte differentiation from human embryonic stem cells (hESC). After treatment with FZHY, albumin expression was consistently increased during dif...

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Autores principales: Chen, Jiamei, Gao, Wei, Zhou, Ping, Ma, Xiaocui, Tschudy-Seney, Benjamin, Liu, Chenghai, Zern, Mark A, Liu, Ping, Duan, Yuyou
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4702137/
https://www.ncbi.nlm.nih.gov/pubmed/26733102
http://dx.doi.org/10.1038/srep18841
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author Chen, Jiamei
Gao, Wei
Zhou, Ping
Ma, Xiaocui
Tschudy-Seney, Benjamin
Liu, Chenghai
Zern, Mark A
Liu, Ping
Duan, Yuyou
author_facet Chen, Jiamei
Gao, Wei
Zhou, Ping
Ma, Xiaocui
Tschudy-Seney, Benjamin
Liu, Chenghai
Zern, Mark A
Liu, Ping
Duan, Yuyou
author_sort Chen, Jiamei
collection PubMed
description Chinese medicine, Fuzhenghuayu (FZHY), appears to prevent fibrosis progression and improve liver function in humans. Here we found that FZHY enhanced hepatocyte differentiation from human embryonic stem cells (hESC). After treatment with FZHY, albumin expression was consistently increased during differentiation and maturation process, and expression of metabolizing enzymes and transporter were also increased. Importantly, expression of mesenchymal cell and cholangiocyte marker was significantly reduced by treatment with FZHY, indicating that one possible mechanism of FZHY’s role is to inhibit the formation of mesenchymal cells and cholangiocytes. Edu-labelled flow cytometric analysis showed that the percentage of the Edu positive cells was increased in the treated cells. These results indicate that the enhanced proliferation involved hepatocytes rather than another cell type. Our investigations further revealed that these enhancements by FZHY are mediated through activation of canonical Wnt and ERK pathways and inhibition of Notch pathway. Thus, FZHY not only promoted hepatocyte differentiation and maturation, but also enhanced hepatocyte proliferation. These results demonstrate that FZHY appears to represent an excellent therapeutic agent for the treatment of liver fibrosis, and that FZHY treatment can enhance our efforts to generate mature hepatocytes with proliferative capacity for cell-based therapeutics and for pharmacological and toxicological studies.
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spelling pubmed-47021372016-01-14 Enhancement of hepatocyte differentiation from human embryonic stem cells by Chinese medicine Fuzhenghuayu Chen, Jiamei Gao, Wei Zhou, Ping Ma, Xiaocui Tschudy-Seney, Benjamin Liu, Chenghai Zern, Mark A Liu, Ping Duan, Yuyou Sci Rep Article Chinese medicine, Fuzhenghuayu (FZHY), appears to prevent fibrosis progression and improve liver function in humans. Here we found that FZHY enhanced hepatocyte differentiation from human embryonic stem cells (hESC). After treatment with FZHY, albumin expression was consistently increased during differentiation and maturation process, and expression of metabolizing enzymes and transporter were also increased. Importantly, expression of mesenchymal cell and cholangiocyte marker was significantly reduced by treatment with FZHY, indicating that one possible mechanism of FZHY’s role is to inhibit the formation of mesenchymal cells and cholangiocytes. Edu-labelled flow cytometric analysis showed that the percentage of the Edu positive cells was increased in the treated cells. These results indicate that the enhanced proliferation involved hepatocytes rather than another cell type. Our investigations further revealed that these enhancements by FZHY are mediated through activation of canonical Wnt and ERK pathways and inhibition of Notch pathway. Thus, FZHY not only promoted hepatocyte differentiation and maturation, but also enhanced hepatocyte proliferation. These results demonstrate that FZHY appears to represent an excellent therapeutic agent for the treatment of liver fibrosis, and that FZHY treatment can enhance our efforts to generate mature hepatocytes with proliferative capacity for cell-based therapeutics and for pharmacological and toxicological studies. Nature Publishing Group 2016-01-06 /pmc/articles/PMC4702137/ /pubmed/26733102 http://dx.doi.org/10.1038/srep18841 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Chen, Jiamei
Gao, Wei
Zhou, Ping
Ma, Xiaocui
Tschudy-Seney, Benjamin
Liu, Chenghai
Zern, Mark A
Liu, Ping
Duan, Yuyou
Enhancement of hepatocyte differentiation from human embryonic stem cells by Chinese medicine Fuzhenghuayu
title Enhancement of hepatocyte differentiation from human embryonic stem cells by Chinese medicine Fuzhenghuayu
title_full Enhancement of hepatocyte differentiation from human embryonic stem cells by Chinese medicine Fuzhenghuayu
title_fullStr Enhancement of hepatocyte differentiation from human embryonic stem cells by Chinese medicine Fuzhenghuayu
title_full_unstemmed Enhancement of hepatocyte differentiation from human embryonic stem cells by Chinese medicine Fuzhenghuayu
title_short Enhancement of hepatocyte differentiation from human embryonic stem cells by Chinese medicine Fuzhenghuayu
title_sort enhancement of hepatocyte differentiation from human embryonic stem cells by chinese medicine fuzhenghuayu
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4702137/
https://www.ncbi.nlm.nih.gov/pubmed/26733102
http://dx.doi.org/10.1038/srep18841
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