Abstract

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.

Highlights

  • Coagulation factor VII (FVII) is a vitamin K-dependent serine protease that is exclusively synthesized by liver

  • FVII mRNA expression is upregulated in cell lines transduced with human FVII-expressing lentivirus

  • FVII mRNA levels were increased in HepG2 and immortalized hepatocyte-like cell line (imHC) infected with human FVII-expressing lentivirus by approximately 31.77-fold and 372.45-fold, respectively, compared with non-transduced cells

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Summary

Introduction

Coagulation factor VII (FVII) is a vitamin K-dependent serine protease that is exclusively synthesized by liver. Human FVII is encoded by the F7 gene on chromosome 13 at 13q34. Mature FVII has a molecular weight of approximately 50 kDa [1] and circulates in plasma in two different forms, the inactive zymogen and the active protease (FVIIa). The inactive zymogen is the major form of FVII and circulates at a concentration of 500 ng/mL, while FVIIa circulates at a significantly lower concentration (~0.5–5.5 ng/mL) [2, 3].

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