Effect of sodium butyrate on the production, heterogeneity and biological activity of human thrombopoietin by recombinant Chinese hamster ovary cells
Abstract
Human thrombopoietin (hTPO) is a heavily glycosylated protein with 6 and 24 potential N- and O-glycosylation sites, respectively. To determine the effect of sodium butyrate (NaBu) on the production and quality of hTPO in recombinant Chinese hamster ovary (rCHO) cells, NaBu (0-10 mM) was added to the cultures of exponentially growing cells. NaBu addition significantly increased both the specific and volumetric hTPO production, although it decreased the cell viability by apoptosis in a dose-dependent manner. The highest hTPO concentration of 82.2 +/- 5.6 microgml-1 was obtained in the culture with 3 mM NaBu addition. Compared with the culture without NaBu addition, the culture with 3 mM NaBu resulted in a 6.4-fold increase in qTPO and a 3.3-fold increase in the final hTPO concentration on day 7. However, NaBu deteriorated the quality of hTPO, resulting from increased heterogeneity, reduced acidic hTPO isoforms, reduced alpha(2 --> 3) sialylation, and decreased in vivo biological activity. We also found that the biological activity of hTPO in the culture with 3 mM NaBu addition collected on day 7 was 72% of that in the culture without NaBu addition. Taken together, the use of NaBu or its optimal concentration for high-level expression of a heavily glycosylated protein like hTPO should be determined by considering its detrimental effect on the quality of glycoprotein.
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Use of histone deacetylase inhibitors such as NaB and VPA may also have undesired secondary effects, such as blocking cell cycle or inducing apoptosis.
“However, the use of these inhibitors may also have undesired secondary effects, such as blocking cell cycle or inducing apoptosis (Sung et al., 2004;Jiang and Sharfstein, 2008;Sunley and Butler, 2010).”
From Therapeutic glycoprotein production in mammalian cells (2017) · cites this paper as Sung et al., 2004
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- Authors
- Sung, Y. H., Song, Y. J., Lim, S. W., Chung, J. Y., & Lee, G. M.
- Affiliations
- Korea Advanced Institute of Science and Technology (KR)
- Daewoong Pharmaceutical (South Korea) (KR)
- Corresponding author
- Lee, Gyun Min
- Venue
- Journal of Biotechnology
- Publisher
- Elsevier BV
- Published
- 2004-09
- Volume
- 112
- Issue
- 3
- Pages
- 323-335
- ISSN
- 0168-1656 (ISSN-L)
- OpenAlex
- W2045486179
- Cited by
- 92
- References
- 1
- Citations by year
- 2026: 1 · 2025: 2 · 2024: 5 · 2022: 2 · 2021: 6 · 2020: 5 · 2019: 6 · 2018: 5 · 2017: 6 · 2016: 2 · 2015: 7 · 2014: 3 · 2013: 3 · 2012: 6
- FWCI
- 1.66
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Biotechnology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Ministry of Education
- Ministry of Science and Technology
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Viral Infectious Diseases and Gene Expression in Insects
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein purification and stability
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Glycosylation and Glycoproteins Research
- Keywords
- thrombopoietin, sodium butyrate, recombinant protein expression, CHO cells, glycosylation, protein heterogeneity, sialylation, protein quality, biological activity, apoptosis, cell viability, glycoprotein expression
- MeSH terms
- Animals, Butyrates, Cell Survival, Cricetulus, Dose-Response Relationship, Drug, Gene Expression Regulation, Cricetinae, Humans, Recombinant Proteins, Sodium, Thrombopoietin, Protein Engineering, CHO Cells, Apoptosis, Cell Culture Techniques, Cell Proliferation
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