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Novel hybrid three-dimensional artificial liver using human induced pluripotent stem cells and a rat decellularized liver scaffold

INTRODUCTION: Liver transplantation is currently the only curative therapy for end-stage liver failure; however, establishment of alternative treatments is required owing to the serious donor organ shortage. Here, we propose a novel model of hybrid three-dimensional artificial livers using both huma...

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Autores principales: Minami, Takahito, Ishii, Takamichi, Yasuchika, Kentaro, Fukumitsu, Ken, Ogiso, Satoshi, Miyauchi, Yuya, Kojima, Hidenobu, Kawai, Takayuki, Yamaoka, Ryoya, Oshima, Yu, Kawamoto, Hiroshi, Kotaka, Maki, Yasuda, Katsutaro, Osafune, Kenji, Uemoto, Shinji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Japanese Society for Regenerative Medicine 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6477477/
https://www.ncbi.nlm.nih.gov/pubmed/31032388
http://dx.doi.org/10.1016/j.reth.2019.03.002
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author Minami, Takahito
Ishii, Takamichi
Yasuchika, Kentaro
Fukumitsu, Ken
Ogiso, Satoshi
Miyauchi, Yuya
Kojima, Hidenobu
Kawai, Takayuki
Yamaoka, Ryoya
Oshima, Yu
Kawamoto, Hiroshi
Kotaka, Maki
Yasuda, Katsutaro
Osafune, Kenji
Uemoto, Shinji
author_facet Minami, Takahito
Ishii, Takamichi
Yasuchika, Kentaro
Fukumitsu, Ken
Ogiso, Satoshi
Miyauchi, Yuya
Kojima, Hidenobu
Kawai, Takayuki
Yamaoka, Ryoya
Oshima, Yu
Kawamoto, Hiroshi
Kotaka, Maki
Yasuda, Katsutaro
Osafune, Kenji
Uemoto, Shinji
author_sort Minami, Takahito
collection PubMed
description INTRODUCTION: Liver transplantation is currently the only curative therapy for end-stage liver failure; however, establishment of alternative treatments is required owing to the serious donor organ shortage. Here, we propose a novel model of hybrid three-dimensional artificial livers using both human induced pluripotent stem cells (hiPSCs) and a rat decellularized liver serving as a scaffold. METHODS: Rat liver harvesting and decellularization were performed as reported in our previous studies. The decellularized liver scaffold was recellularized with hiPSC-derived hepatocyte-like cells (hiPSC-HLCs) through the biliary duct. The recellularized liver graft was continuously perfused with the culture medium using a pump at a flow rate of 0.5 mL/min in a standard CO(2) (5%) cell incubator at 37 °C. RESULTS: After 48 h of continuous perfusion culture, the hiPSC-HLCs of the recellularized liver distributed into the parenchymal space. Furthermore, the recellularized liver expressed the albumin (ALB) and CYP3A4 genes, and secreted human ALB into the culture medium. CONCLUSION: Novel hybrid artificial livers using hiPSCs and rat decellularized liver scaffolds were successfully generated, which possessed human hepatic functions.
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spelling pubmed-64774772019-04-26 Novel hybrid three-dimensional artificial liver using human induced pluripotent stem cells and a rat decellularized liver scaffold Minami, Takahito Ishii, Takamichi Yasuchika, Kentaro Fukumitsu, Ken Ogiso, Satoshi Miyauchi, Yuya Kojima, Hidenobu Kawai, Takayuki Yamaoka, Ryoya Oshima, Yu Kawamoto, Hiroshi Kotaka, Maki Yasuda, Katsutaro Osafune, Kenji Uemoto, Shinji Regen Ther Original Article INTRODUCTION: Liver transplantation is currently the only curative therapy for end-stage liver failure; however, establishment of alternative treatments is required owing to the serious donor organ shortage. Here, we propose a novel model of hybrid three-dimensional artificial livers using both human induced pluripotent stem cells (hiPSCs) and a rat decellularized liver serving as a scaffold. METHODS: Rat liver harvesting and decellularization were performed as reported in our previous studies. The decellularized liver scaffold was recellularized with hiPSC-derived hepatocyte-like cells (hiPSC-HLCs) through the biliary duct. The recellularized liver graft was continuously perfused with the culture medium using a pump at a flow rate of 0.5 mL/min in a standard CO(2) (5%) cell incubator at 37 °C. RESULTS: After 48 h of continuous perfusion culture, the hiPSC-HLCs of the recellularized liver distributed into the parenchymal space. Furthermore, the recellularized liver expressed the albumin (ALB) and CYP3A4 genes, and secreted human ALB into the culture medium. CONCLUSION: Novel hybrid artificial livers using hiPSCs and rat decellularized liver scaffolds were successfully generated, which possessed human hepatic functions. Japanese Society for Regenerative Medicine 2019-03-30 /pmc/articles/PMC6477477/ /pubmed/31032388 http://dx.doi.org/10.1016/j.reth.2019.03.002 Text en © 2019 The Japanese Society for Regenerative Medicine. Production and hosting by Elsevier B.V. http://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 Article
Minami, Takahito
Ishii, Takamichi
Yasuchika, Kentaro
Fukumitsu, Ken
Ogiso, Satoshi
Miyauchi, Yuya
Kojima, Hidenobu
Kawai, Takayuki
Yamaoka, Ryoya
Oshima, Yu
Kawamoto, Hiroshi
Kotaka, Maki
Yasuda, Katsutaro
Osafune, Kenji
Uemoto, Shinji
Novel hybrid three-dimensional artificial liver using human induced pluripotent stem cells and a rat decellularized liver scaffold
title Novel hybrid three-dimensional artificial liver using human induced pluripotent stem cells and a rat decellularized liver scaffold
title_full Novel hybrid three-dimensional artificial liver using human induced pluripotent stem cells and a rat decellularized liver scaffold
title_fullStr Novel hybrid three-dimensional artificial liver using human induced pluripotent stem cells and a rat decellularized liver scaffold
title_full_unstemmed Novel hybrid three-dimensional artificial liver using human induced pluripotent stem cells and a rat decellularized liver scaffold
title_short Novel hybrid three-dimensional artificial liver using human induced pluripotent stem cells and a rat decellularized liver scaffold
title_sort novel hybrid three-dimensional artificial liver using human induced pluripotent stem cells and a rat decellularized liver scaffold
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6477477/
https://www.ncbi.nlm.nih.gov/pubmed/31032388
http://dx.doi.org/10.1016/j.reth.2019.03.002
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