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Efficient generation of hepatic cells from mesenchymal stromal cells by an innovative bio-microfluidic cell culture device

BACKGROUND: Mesenchymal stromal cells (MSCs) are multipotent and have great potential in cell therapy. Previously we reported the differentiation potential of human MSCs into hepatocytes in vitro and that these cells can rescue fulminant hepatic failure. However, the conventional static culture meth...

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Autores principales: Yen, Meng-Hua, Wu, Yuan-Yi, Liu, Yi-Shiuan, Rimando, Marilyn, Ho, Jennifer Hui-Chun, Lee, Oscar Kuang-Sheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4992324/
https://www.ncbi.nlm.nih.gov/pubmed/27542358
http://dx.doi.org/10.1186/s13287-016-0371-7
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author Yen, Meng-Hua
Wu, Yuan-Yi
Liu, Yi-Shiuan
Rimando, Marilyn
Ho, Jennifer Hui-Chun
Lee, Oscar Kuang-Sheng
author_facet Yen, Meng-Hua
Wu, Yuan-Yi
Liu, Yi-Shiuan
Rimando, Marilyn
Ho, Jennifer Hui-Chun
Lee, Oscar Kuang-Sheng
author_sort Yen, Meng-Hua
collection PubMed
description BACKGROUND: Mesenchymal stromal cells (MSCs) are multipotent and have great potential in cell therapy. Previously we reported the differentiation potential of human MSCs into hepatocytes in vitro and that these cells can rescue fulminant hepatic failure. However, the conventional static culture method neither maintains growth factors at an optimal level constantly nor removes cellular waste efficiently. In addition, not only is the duration of differentiating hepatocyte lineage cells from MSCs required to improve, but also the need for a large number of hepatocytes for cell therapy has not to date been addressed fully. The purpose of this study is to design and develop an innovative microfluidic device to overcome these shortcomings. METHODS: We designed and fabricated a microfluidic device and a culture system for hepatic differentiation of MSCs using our protocol reported previously. The microfluidic device contains a large culture chamber with a stable uniform flow to allow homogeneous distribution and expansion as well as efficient induction of hepatic differentiation for MSCs. RESULTS: The device enables real-time observation under light microscopy and exhibits a better differentiation efficiency for MSCs compared with conventional static culture. MSCs grown in the microfluidic device showed a higher level of hepatocyte marker gene expression under hepatic induction. Functional analysis of hepatic differentiation demonstrated significantly higher urea production in the microfluidic device after 21 days of hepatic differentiation. CONCLUSIONS: The microfluidic device allows the generation of a large number of MSCs and induces hepatic differentiation of MSCs efficiently. The device can be adapted for scale-up production of hepatic cells from MSCs for cellular therapy. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13287-016-0371-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-49923242016-08-21 Efficient generation of hepatic cells from mesenchymal stromal cells by an innovative bio-microfluidic cell culture device Yen, Meng-Hua Wu, Yuan-Yi Liu, Yi-Shiuan Rimando, Marilyn Ho, Jennifer Hui-Chun Lee, Oscar Kuang-Sheng Stem Cell Res Ther Research BACKGROUND: Mesenchymal stromal cells (MSCs) are multipotent and have great potential in cell therapy. Previously we reported the differentiation potential of human MSCs into hepatocytes in vitro and that these cells can rescue fulminant hepatic failure. However, the conventional static culture method neither maintains growth factors at an optimal level constantly nor removes cellular waste efficiently. In addition, not only is the duration of differentiating hepatocyte lineage cells from MSCs required to improve, but also the need for a large number of hepatocytes for cell therapy has not to date been addressed fully. The purpose of this study is to design and develop an innovative microfluidic device to overcome these shortcomings. METHODS: We designed and fabricated a microfluidic device and a culture system for hepatic differentiation of MSCs using our protocol reported previously. The microfluidic device contains a large culture chamber with a stable uniform flow to allow homogeneous distribution and expansion as well as efficient induction of hepatic differentiation for MSCs. RESULTS: The device enables real-time observation under light microscopy and exhibits a better differentiation efficiency for MSCs compared with conventional static culture. MSCs grown in the microfluidic device showed a higher level of hepatocyte marker gene expression under hepatic induction. Functional analysis of hepatic differentiation demonstrated significantly higher urea production in the microfluidic device after 21 days of hepatic differentiation. CONCLUSIONS: The microfluidic device allows the generation of a large number of MSCs and induces hepatic differentiation of MSCs efficiently. The device can be adapted for scale-up production of hepatic cells from MSCs for cellular therapy. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13287-016-0371-7) contains supplementary material, which is available to authorized users. BioMed Central 2016-08-19 /pmc/articles/PMC4992324/ /pubmed/27542358 http://dx.doi.org/10.1186/s13287-016-0371-7 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Yen, Meng-Hua
Wu, Yuan-Yi
Liu, Yi-Shiuan
Rimando, Marilyn
Ho, Jennifer Hui-Chun
Lee, Oscar Kuang-Sheng
Efficient generation of hepatic cells from mesenchymal stromal cells by an innovative bio-microfluidic cell culture device
title Efficient generation of hepatic cells from mesenchymal stromal cells by an innovative bio-microfluidic cell culture device
title_full Efficient generation of hepatic cells from mesenchymal stromal cells by an innovative bio-microfluidic cell culture device
title_fullStr Efficient generation of hepatic cells from mesenchymal stromal cells by an innovative bio-microfluidic cell culture device
title_full_unstemmed Efficient generation of hepatic cells from mesenchymal stromal cells by an innovative bio-microfluidic cell culture device
title_short Efficient generation of hepatic cells from mesenchymal stromal cells by an innovative bio-microfluidic cell culture device
title_sort efficient generation of hepatic cells from mesenchymal stromal cells by an innovative bio-microfluidic cell culture device
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4992324/
https://www.ncbi.nlm.nih.gov/pubmed/27542358
http://dx.doi.org/10.1186/s13287-016-0371-7
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