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Stable overexpression of arginase I and ornithine transcarbamylase in HepG2 cells improves its ammonia detoxification
Author(s) -
Tang Nanhong,
Wang Yan,
Wang Xiaoqian,
Zhou Liangyi,
Zhang Feiyuan,
Li Xiujin,
Chen Yanlin
Publication year - 2012
Publication title -
journal of cellular biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.028
H-Index - 165
eISSN - 1097-4644
pISSN - 0730-2312
DOI - 10.1002/jcb.23375
Subject(s) - arginase , ornithine transcarbamylase , bioartificial liver device , carbamoyl phosphate synthetase , cell culture , glutamine synthetase , enzyme , glutamine , biochemistry , ammonia , microbiology and biotechnology , urea cycle , cell , biology , detoxification (alternative medicine) , hepatocyte , chemistry , arginine , in vitro , amino acid , medicine , genetics , alternative medicine , pathology
HepG2 is an immortalized human hepatoma cell line that has been used for research into bioartificial liver systems. However, a low level of ammonia detoxification is its biggest drawback. In this work, a recombinant HepG2 cell line with stable overexpression of human arginase I (hArgI) and human ornithine transcarbamylase (hOTC), HepG2/(hArgI + hOTC)4, was developed using a eukaryotic dual gene expression vector pBudCE4.1. (1) The hArgI and hOTC enzymatic activity in HepG2/(hArgI + hOTC)4 cells were higher than in the control cells. (2) The ammonia tolerance capacity of HepG2/(hArgI + hOTC)4 cells was three times that of HepG2 cells and 37.5% of that of primary human hepatocytes in cultivation. In the experiment of ammonia detoxification, HepG2/(hArgI + hOTC)4 cells produced 3.1 times more urea (at 180 mM NH 4 Cl) and 3.1 times more glutamine (at 120 mM NH 4 Cl and 15 mM glutamate) than HepG2 cells, reaching 63.1% and 36.0% that of primary human hepatocytes, respectively. (3) The hArgI and hOTC overexpression did not influence the growth of HepG2 cells and also promoted the expression of other ammonia detoxification associated proteins including glutamine synthetase (GS), arginase II (ArgII), arginosuccinate synthase (ASS) and arginosuccinate lyase (ASL) in HepG2 cells. This work illustrates that the modification reported here made significant progress in the improvement of HepG2 cell function and the HepG2/(hArgI + hOTC)4 cells will provide a better selection for the application of bioartificial liver system. J. Cell. Biochem. 113: 518–527, 2012. © 2011 Wiley Periodicals, Inc.