Coagulant activity of recombinant human factor VII produced by lentiviral human F7 gene transfer in immortalized hepatocyte-like cell line.
Sarai PongjantarasatianPraguywan KadegasemWerasak SasanakulKhanit Sa-NgiamsuntornSuparerk BorwornpinyoNongnuch SirachainanAmpaiwan ChuansumritPansakorn TanratanaSuradej HongengPublished in: PloS one (2019)
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.
Keyphrases
- endothelial cells
- mesenchymal stem cells
- induced pluripotent stem cells
- liver injury
- healthcare
- single cell
- cell therapy
- human health
- stem cells
- gene expression
- risk assessment
- cell cycle arrest
- genome wide
- drug induced
- cell death
- bone marrow
- copy number
- dna methylation
- cell proliferation
- small molecule
- climate change
- binding protein