The viability of primary hepatocytes is maintained under a low cysteine-glutathione redox state with a marked elevation in ophthalmic acid production

Extracellular cystine, the oxidized form of cysteine (Cys), is taken up by cells via the cystine transporter xCT. xCT is not expressed in the liver but is induced in primary hepatocytes under conventional cultured conditions. However, compared to wild-type hepatocytes those from the xCT-knockout mou...

Full description

Saved in:
Bibliographic Details
Published inExperimental cell research Vol. 361; no. 1; pp. 178 - 191
Main Authors Lee, Jaeyong, Kang, Eun Sil, Kobayashi, Sho, Homma, Takujiro, Sato, Hideyo, Seo, Han Geuk, Fujii, Junichi
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.12.2017
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Extracellular cystine, the oxidized form of cysteine (Cys), is taken up by cells via the cystine transporter xCT. xCT is not expressed in the liver but is induced in primary hepatocytes under conventional cultured conditions. However, compared to wild-type hepatocytes those from the xCT-knockout mouse showed no evidence of an abnormality and the levels of both Cys and glutathione (GSH) remained unchanged. The levels of ophthalmic acid (OPT), which is produced as an alternative compound by the GSH-synthesizing pathway, became increased during the culturing of hepatocytes. It therefore appears that, in primary hepatocytes, Cys is provided by systems other than xCT, most likely via the transsulfuration pathway, but the levels that are produced are not sufficient. We also employed mouse hepatoma-derived Hepa1-6 cells, which constitutively express xCT. When Hepa 1-6 cells were cultivated in Cys-free media, the levels of intracellular Cys and GSH were decreased, compared to cells cultured in conventional media, leading to cell death accompanied by an increase in the levels of reactive oxygen species and lipid peroxidation products with characteristics similar to ferroptosis. While OPT levels were increased by only to a limited extent in Hepa 1-6 cells, primary hepatocytes cultured in Cys- and Met-free media showed a marked elevation in OPT, reaching levels nearly equivalent to the GSH levels when the cells were cultured in conventional media. Thus, OPT may become a marker for Cys insufficiency and might be used to predict pathological conditions of cells with elevated oxidative stress. Differential cysteine-supply systems between the primary mouse hepatocytes and Hepa 1-6 cells under conventional or Cys/Met-free culture. Met; Methionine, Hcy; Homocysteine, Cst; Cystathionine, Cys; Cysteine, Thr; Threonine, Glu; Glutamate, 2OB; 2-Oxo-butyric acid, 2AB; 2-Amino-butyric acid, GSH; Glutathione, OPT; Ophthalmic acid, γGCS; γ-Glutamylcysteine synthetase, GS; Glutathione synthetase; NAAT; neutral amino acid transporter [Display omitted] •xCT is induced in primary mouse hepatocytes under culture conditions.•xCT-KO hepatocytes contained normal levels of cysteine and glutathione (GSH).•Primary hepatocytes were viable in cysteine- and methionine-free media.•Ophthalmic acid levels were equivalent to those of GSH in hepatocytes.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0014-4827
1090-2422
DOI:10.1016/j.yexcr.2017.10.017