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Coagulant activity of recombinant human factor VII produced by lentiviral human F7 gene transfer in immortalized hepatocyte-like cell line
Human mesenchymal stem cells (hMSCs) have the potential to differentiate into hepatocyte-like cells, indicating that these cells may be the new target cell of interest to produce biopharmaceuticals. Our group recently established a hMSC-derived immortalized hepatocyte-like cell line (imHC) that demo...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6681952/ https://www.ncbi.nlm.nih.gov/pubmed/31381603 http://dx.doi.org/10.1371/journal.pone.0220825 |
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author | Pongjantarasatian, Sarai Kadegasem, Praguywan Sasanakul, Werasak Sa-ngiamsuntorn, Khanit Borwornpinyo, Suparerk Sirachainan, Nongnuch Chuansumrit, Ampaiwan Tanratana, Pansakorn Hongeng, Suradej |
author_facet | Pongjantarasatian, Sarai Kadegasem, Praguywan Sasanakul, Werasak Sa-ngiamsuntorn, Khanit Borwornpinyo, Suparerk Sirachainan, Nongnuch Chuansumrit, Ampaiwan Tanratana, Pansakorn Hongeng, Suradej |
author_sort | Pongjantarasatian, Sarai |
collection | PubMed |
description | Human mesenchymal stem cells (hMSCs) have the potential to differentiate into hepatocyte-like cells, indicating that these cells may be the new target cell of interest to produce biopharmaceuticals. Our group recently established a hMSC-derived immortalized hepatocyte-like cell line (imHC) that demonstrates several liver-specific phenotypes. However, the ability of imHC to produce coagulation factors has not been characterized. Here, we examined the potential for imHC as a source of coagulation protein production by investigating the ability of imHC to produce human factor VII (FVII) using a lentiviral transduction system. Our results showed that imHC secreted a low amount of FVII (~22 ng/mL) into culture supernatant. Moreover, FVII from the transduced imHC (0.11 ± 0.005 IU/mL) demonstrated a similar coagulant activity compared with FVII from transduced HEK293T cells (0.12 ± 0.004 IU/mL) as determined by chromogenic assay. We demonstrate for the first time, to the best of our knowledge, that imHC produced FVII, albeit at a low level, indicating the unique characteristic of hepatocytes. Our study suggests the possibility of using imHC for the production of coagulation proteins. |
format | Online Article Text |
id | pubmed-6681952 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-66819522019-08-15 Coagulant activity of recombinant human factor VII produced by lentiviral human F7 gene transfer in immortalized hepatocyte-like cell line Pongjantarasatian, Sarai Kadegasem, Praguywan Sasanakul, Werasak Sa-ngiamsuntorn, Khanit Borwornpinyo, Suparerk Sirachainan, Nongnuch Chuansumrit, Ampaiwan Tanratana, Pansakorn Hongeng, Suradej PLoS One Research Article Human mesenchymal stem cells (hMSCs) have the potential to differentiate into hepatocyte-like cells, indicating that these cells may be the new target cell of interest to produce biopharmaceuticals. Our group recently established a hMSC-derived immortalized hepatocyte-like cell line (imHC) that demonstrates several liver-specific phenotypes. However, the ability of imHC to produce coagulation factors has not been characterized. Here, we examined the potential for imHC as a source of coagulation protein production by investigating the ability of imHC to produce human factor VII (FVII) using a lentiviral transduction system. Our results showed that imHC secreted a low amount of FVII (~22 ng/mL) into culture supernatant. Moreover, FVII from the transduced imHC (0.11 ± 0.005 IU/mL) demonstrated a similar coagulant activity compared with FVII from transduced HEK293T cells (0.12 ± 0.004 IU/mL) as determined by chromogenic assay. We demonstrate for the first time, to the best of our knowledge, that imHC produced FVII, albeit at a low level, indicating the unique characteristic of hepatocytes. Our study suggests the possibility of using imHC for the production of coagulation proteins. Public Library of Science 2019-08-05 /pmc/articles/PMC6681952/ /pubmed/31381603 http://dx.doi.org/10.1371/journal.pone.0220825 Text en © 2019 Pongjantarasatian et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Pongjantarasatian, Sarai Kadegasem, Praguywan Sasanakul, Werasak Sa-ngiamsuntorn, Khanit Borwornpinyo, Suparerk Sirachainan, Nongnuch Chuansumrit, Ampaiwan Tanratana, Pansakorn Hongeng, Suradej Coagulant activity of recombinant human factor VII produced by lentiviral human F7 gene transfer in immortalized hepatocyte-like cell line |
title | Coagulant activity of recombinant human factor VII produced by lentiviral human F7 gene transfer in immortalized hepatocyte-like cell line |
title_full | Coagulant activity of recombinant human factor VII produced by lentiviral human F7 gene transfer in immortalized hepatocyte-like cell line |
title_fullStr | Coagulant activity of recombinant human factor VII produced by lentiviral human F7 gene transfer in immortalized hepatocyte-like cell line |
title_full_unstemmed | Coagulant activity of recombinant human factor VII produced by lentiviral human F7 gene transfer in immortalized hepatocyte-like cell line |
title_short | Coagulant activity of recombinant human factor VII produced by lentiviral human F7 gene transfer in immortalized hepatocyte-like cell line |
title_sort | coagulant activity of recombinant human factor vii produced by lentiviral human f7 gene transfer in immortalized hepatocyte-like cell line |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6681952/ https://www.ncbi.nlm.nih.gov/pubmed/31381603 http://dx.doi.org/10.1371/journal.pone.0220825 |
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