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Investigation of the effects of urea cycle amino acids on the expression of ALB and CEBPB in the human hepatocellular carcinoma cell line FLC-4

Cell lines are powerful tools for research into liver function at the molecular level. However, they are generally unsuitable for rigorously assessing the effects of amino acid composition, because many lines require serum-containing medium for their maintenance. Here, we aimed to investigate the ef...

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Autores principales: Fujimi, Takahiko J., Mezaki, Yoshihiro, Masaki, Takahiro, Tajima, Ayasa, Nakamura, Mariko, Yoshikawa, Akira, Murai, Noriyuki, Aizawa, Mamoru, Kojima, Soichi, Matsumoto, Yoshihiro, Aizaki, Hideki, Matsuura, Tomokazu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Singapore 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7324429/
https://www.ncbi.nlm.nih.gov/pubmed/32474770
http://dx.doi.org/10.1007/s13577-020-00383-1
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author Fujimi, Takahiko J.
Mezaki, Yoshihiro
Masaki, Takahiro
Tajima, Ayasa
Nakamura, Mariko
Yoshikawa, Akira
Murai, Noriyuki
Aizawa, Mamoru
Kojima, Soichi
Matsumoto, Yoshihiro
Aizaki, Hideki
Matsuura, Tomokazu
author_facet Fujimi, Takahiko J.
Mezaki, Yoshihiro
Masaki, Takahiro
Tajima, Ayasa
Nakamura, Mariko
Yoshikawa, Akira
Murai, Noriyuki
Aizawa, Mamoru
Kojima, Soichi
Matsumoto, Yoshihiro
Aizaki, Hideki
Matsuura, Tomokazu
author_sort Fujimi, Takahiko J.
collection PubMed
description Cell lines are powerful tools for research into liver function at the molecular level. However, they are generally unsuitable for rigorously assessing the effects of amino acid composition, because many lines require serum-containing medium for their maintenance. Here, we aimed to investigate the effects of ornithine and arginine, which are included in the characteristic metabolic process in hepatocyte, on a human hepatoma-derived cell line (FLC-4) that can be cultured in serum-free medium. FLC-4 cells were cultured under the following three conditions: + ornithine/ – arginine, – ornithine/ – arginine, and –ornithine/ + arginine. Albumin expression evaluated by quantitative polymerase chain reaction and enzyme-linked immunosorbent assay and showed no obvious differences based on the presence of ornithine or arginine. However, the mRNA levels of two liver-enriched transcription factors (CEBPB and HNF1A), which are involved in regulating albumin expression, were significantly higher in cells grown in medium-containing arginine than that in cells grown in ornithine-containing medium. Western blotting showed that the levels both activating and inhibitory C/EBPβ isoforms were significantly increased in cells grown in arginine medium. Furthermore, we have found that depletion of both ornithine and arginine, the polyamine sources, in the medium did not cause polyamine deficiency. When ornithine and arginine were depleted, albumin production was significantly reduced at the mRNA level, CEBPB mRNA levels were increased, and the level of activating form of C/EBPβ was increased. The results of this study suggest that in hepatocyte, these two amino acids might have different functions, and because of which they elicit disparate cellular responses. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s13577-020-00383-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-73244292020-07-07 Investigation of the effects of urea cycle amino acids on the expression of ALB and CEBPB in the human hepatocellular carcinoma cell line FLC-4 Fujimi, Takahiko J. Mezaki, Yoshihiro Masaki, Takahiro Tajima, Ayasa Nakamura, Mariko Yoshikawa, Akira Murai, Noriyuki Aizawa, Mamoru Kojima, Soichi Matsumoto, Yoshihiro Aizaki, Hideki Matsuura, Tomokazu Hum Cell Research Article Cell lines are powerful tools for research into liver function at the molecular level. However, they are generally unsuitable for rigorously assessing the effects of amino acid composition, because many lines require serum-containing medium for their maintenance. Here, we aimed to investigate the effects of ornithine and arginine, which are included in the characteristic metabolic process in hepatocyte, on a human hepatoma-derived cell line (FLC-4) that can be cultured in serum-free medium. FLC-4 cells were cultured under the following three conditions: + ornithine/ – arginine, – ornithine/ – arginine, and –ornithine/ + arginine. Albumin expression evaluated by quantitative polymerase chain reaction and enzyme-linked immunosorbent assay and showed no obvious differences based on the presence of ornithine or arginine. However, the mRNA levels of two liver-enriched transcription factors (CEBPB and HNF1A), which are involved in regulating albumin expression, were significantly higher in cells grown in medium-containing arginine than that in cells grown in ornithine-containing medium. Western blotting showed that the levels both activating and inhibitory C/EBPβ isoforms were significantly increased in cells grown in arginine medium. Furthermore, we have found that depletion of both ornithine and arginine, the polyamine sources, in the medium did not cause polyamine deficiency. When ornithine and arginine were depleted, albumin production was significantly reduced at the mRNA level, CEBPB mRNA levels were increased, and the level of activating form of C/EBPβ was increased. The results of this study suggest that in hepatocyte, these two amino acids might have different functions, and because of which they elicit disparate cellular responses. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s13577-020-00383-1) contains supplementary material, which is available to authorized users. Springer Singapore 2020-05-30 2020 /pmc/articles/PMC7324429/ /pubmed/32474770 http://dx.doi.org/10.1007/s13577-020-00383-1 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Research Article
Fujimi, Takahiko J.
Mezaki, Yoshihiro
Masaki, Takahiro
Tajima, Ayasa
Nakamura, Mariko
Yoshikawa, Akira
Murai, Noriyuki
Aizawa, Mamoru
Kojima, Soichi
Matsumoto, Yoshihiro
Aizaki, Hideki
Matsuura, Tomokazu
Investigation of the effects of urea cycle amino acids on the expression of ALB and CEBPB in the human hepatocellular carcinoma cell line FLC-4
title Investigation of the effects of urea cycle amino acids on the expression of ALB and CEBPB in the human hepatocellular carcinoma cell line FLC-4
title_full Investigation of the effects of urea cycle amino acids on the expression of ALB and CEBPB in the human hepatocellular carcinoma cell line FLC-4
title_fullStr Investigation of the effects of urea cycle amino acids on the expression of ALB and CEBPB in the human hepatocellular carcinoma cell line FLC-4
title_full_unstemmed Investigation of the effects of urea cycle amino acids on the expression of ALB and CEBPB in the human hepatocellular carcinoma cell line FLC-4
title_short Investigation of the effects of urea cycle amino acids on the expression of ALB and CEBPB in the human hepatocellular carcinoma cell line FLC-4
title_sort investigation of the effects of urea cycle amino acids on the expression of alb and cebpb in the human hepatocellular carcinoma cell line flc-4
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7324429/
https://www.ncbi.nlm.nih.gov/pubmed/32474770
http://dx.doi.org/10.1007/s13577-020-00383-1
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