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In vitro ballooned hepatocytes can be produced by primary human hepatocytes and hepatic stellate cell sheets

Despite the increasing prevalence of Nonalcoholic steatohepatitis (NASH) worldwide, there is no effective treatment available for this disease. “Ballooned hepatocyte” is a characteristic finding in NASH and is correlated with disease prognosis, but their mechanisms of action are poorly understood; f...

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Autores principales: Hasui, Nobuhiro, Sakaguchi, Katsuhisa, Ogawa, Tetsuya, Sakamoto, Yoshihiro, Shimizu, Tatsuya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8964766/
https://www.ncbi.nlm.nih.gov/pubmed/35351975
http://dx.doi.org/10.1038/s41598-022-09428-x
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author Hasui, Nobuhiro
Sakaguchi, Katsuhisa
Ogawa, Tetsuya
Sakamoto, Yoshihiro
Shimizu, Tatsuya
author_facet Hasui, Nobuhiro
Sakaguchi, Katsuhisa
Ogawa, Tetsuya
Sakamoto, Yoshihiro
Shimizu, Tatsuya
author_sort Hasui, Nobuhiro
collection PubMed
description Despite the increasing prevalence of Nonalcoholic steatohepatitis (NASH) worldwide, there is no effective treatment available for this disease. “Ballooned hepatocyte” is a characteristic finding in NASH and is correlated with disease prognosis, but their mechanisms of action are poorly understood; furthermore, neither animal nor in vitro models of NASH have been able to adequately represent ballooned hepatocytes. Herein, we engineered cell sheets to develop a new in vitro model of ballooned hepatocytes. Primary human hepatocytes (PHH) and Hepatic stellate cells (HSC) were co-cultured to produce cell sheets, which were cultured in glucose and lipid containing medium, following which histological and functional analyses were performed. Histological findings showed hepatocyte ballooning, accumulation of fat droplets, abnormal cytokeratin arrangement, and the presence of Mallory–Denk bodies and abnormal organelles. These findings are similar to those of ballooned hepatocytes in human NASH. Functional analysis showed elevated levels of TGFβ-1, SHH, and p62, but not TNF-α, IL-8. Exposure of PHH/HSC sheets to a glucolipotoxicity environment induces ballooned hepatocyte without inflammation. Moreover, fibrosis is an important mechanism underlying ballooned hepatocytes and could be the basis for the development of a new in vitro NASH model with ballooned hepatocytes.
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spelling pubmed-89647662022-03-30 In vitro ballooned hepatocytes can be produced by primary human hepatocytes and hepatic stellate cell sheets Hasui, Nobuhiro Sakaguchi, Katsuhisa Ogawa, Tetsuya Sakamoto, Yoshihiro Shimizu, Tatsuya Sci Rep Article Despite the increasing prevalence of Nonalcoholic steatohepatitis (NASH) worldwide, there is no effective treatment available for this disease. “Ballooned hepatocyte” is a characteristic finding in NASH and is correlated with disease prognosis, but their mechanisms of action are poorly understood; furthermore, neither animal nor in vitro models of NASH have been able to adequately represent ballooned hepatocytes. Herein, we engineered cell sheets to develop a new in vitro model of ballooned hepatocytes. Primary human hepatocytes (PHH) and Hepatic stellate cells (HSC) were co-cultured to produce cell sheets, which were cultured in glucose and lipid containing medium, following which histological and functional analyses were performed. Histological findings showed hepatocyte ballooning, accumulation of fat droplets, abnormal cytokeratin arrangement, and the presence of Mallory–Denk bodies and abnormal organelles. These findings are similar to those of ballooned hepatocytes in human NASH. Functional analysis showed elevated levels of TGFβ-1, SHH, and p62, but not TNF-α, IL-8. Exposure of PHH/HSC sheets to a glucolipotoxicity environment induces ballooned hepatocyte without inflammation. Moreover, fibrosis is an important mechanism underlying ballooned hepatocytes and could be the basis for the development of a new in vitro NASH model with ballooned hepatocytes. Nature Publishing Group UK 2022-03-29 /pmc/articles/PMC8964766/ /pubmed/35351975 http://dx.doi.org/10.1038/s41598-022-09428-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Hasui, Nobuhiro
Sakaguchi, Katsuhisa
Ogawa, Tetsuya
Sakamoto, Yoshihiro
Shimizu, Tatsuya
In vitro ballooned hepatocytes can be produced by primary human hepatocytes and hepatic stellate cell sheets
title In vitro ballooned hepatocytes can be produced by primary human hepatocytes and hepatic stellate cell sheets
title_full In vitro ballooned hepatocytes can be produced by primary human hepatocytes and hepatic stellate cell sheets
title_fullStr In vitro ballooned hepatocytes can be produced by primary human hepatocytes and hepatic stellate cell sheets
title_full_unstemmed In vitro ballooned hepatocytes can be produced by primary human hepatocytes and hepatic stellate cell sheets
title_short In vitro ballooned hepatocytes can be produced by primary human hepatocytes and hepatic stellate cell sheets
title_sort in vitro ballooned hepatocytes can be produced by primary human hepatocytes and hepatic stellate cell sheets
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8964766/
https://www.ncbi.nlm.nih.gov/pubmed/35351975
http://dx.doi.org/10.1038/s41598-022-09428-x
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