Abstract
An analog of aromatic cytokinins, the 2,6,9-trisubstituted purine derivative bohemine, was applied to cultures of mouse hybridoma cells in order to analyze its capacity of suppressing cell growth and maintaining or enhancing the production of monoclonal antibody. Addition of bohemine at concentrations in the range of1–10 μM resulted in a short-term arrest of growth and of monoclonal antibody production. The short-term suppression of cell functions was followed by a significant temporary increase of specific growth rate and of specific production rate. The steady-state viable cell density values, found in semicontinuous cultures, showed a certain stimulation of cell growth in the range of micromolar concentrations of bohemine, and inhibition of growth at 10 and 30 μM concentrations. The profiles of cell cycle phases indicated that hybridoma cells are retarded both at the G1/S boundary and at the G2/M boundary, depending on bohemine concentration. The existence of the sequence of events,from suppression to stimulation, suggests that bohemine probably modulates more than one regulatory pathway in the cell.
Keywords: cell cycle, fed-batch culture, hybridoma, purine derivatives, semicontinuous culture
Full Text
The Full Text of this article is available as a PDF (118.6 KB).
References
- Alberio R, Kubelka M, Zakhartchenko V, Hajdúch M, Wolf E, Motlík J. Activation of bovine oocytes by specific inhibition of cyclin-dependent kinases. Mol Reprod Dev. 2000;55:422–432. doi: 10.1002/(SICI)1098-2795(200004)55:4<422::AID-MRD10>3.0.CO;2-C. [DOI] [PubMed] [Google Scholar]
- Chang Y-T, Gray NS, Rosania GR, Sutherlin DP, Kwon S, Norman TC, Sarohia R, Leost M, Meijer L, Schultz PG. Synthesis and application of functionally diverse 2,6,9-trisubstituted purine libraries as CDK inhibitors. Chem Biol. 1999;6:361–375. doi: 10.1016/S1074-5521(99)80048-9. [DOI] [PubMed] [Google Scholar]
- Chmela Z, Veselý J, Lemr K, Rypka M, Hanuš J, Havlíček L, Kryštof V, Michnová L, Fuksová K, Lukeš J. In vivo metabolism of 2,6,9-trisubstituted purine-derived cyclindependent kinase inhibitor bohemine in mice: glucosidation as the principal metabolic route. Drug Metabol Disp. 2001;vn29:326–334. [PubMed] [Google Scholar]
- De Azevedo WF, Leclerc S, Meijer L, Havlíček L, Strnad M, Kim SH. Inhibition of cyclin-dependent kinases by purine analogues: Crystal structure of human cdk2 complexed with roscovitine. Eur J Biochem. 1997;243:318–326. doi: 10.1111/j.1432-1033.1997.0518a.x. [DOI] [PubMed] [Google Scholar]
- Fenge C, Fraune E, Freitag R, Scheper T, Schügerl K. On-line monitoring of monoclonal antibody formation in highdensity perfusion culture using FIA. Cytotechnology. 1991;6:55–63. doi: 10.1007/BF00353703. [DOI] [PubMed] [Google Scholar]
- Franěk F, Holý A, Votruba I, Eckschlager T. Modulation of cell cycle progression and of antibody production in mouse hybridomas by a nucleotide analogue. Cytotechnology. 1998;28:65–72. doi: 10.1023/A:1008017328061. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Frančk F, Šrámková K. Cell suicide in starving hybridoma culture: Survival-signal effect of some amino acids. Cytotechnology. 1996;21:81–89. doi: 10.1007/BF00364839. [DOI] [PubMed] [Google Scholar]
- Frančk F, Vomastek T, Dolníková J. Fragmented DNA and apoptotic bodies document the programmed way of cell death in hybridoma cultures. Cytotechnology. 1992;9:117–123. doi: 10.1007/BF02521738. [DOI] [PubMed] [Google Scholar]
- Fussenegger M, Mazur X, Bailey JE. A novel cytostatic process enhances the productivity of Chinese hamster ovary cells. Biotechnol Bioeng. 1997;55:927–939. doi: 10.1002/(SICI)1097-0290(19970920)55:6<927::AID-BIT10>3.0.CO;2-4. [DOI] [PubMed] [Google Scholar]
- Hajdúch M, Havlíček L, Veselý J, Novotný R, Mihál V, Strnad M. Synthetic cyclin-dependent kinase inhibitors. New generation of potent anti-cancer drugs. In: Pieters R, Veerman A, Kaspers GJL, editors. Advances in Experimental Medicine and Biology. Plenum Press: New York; 1999. pp. 341–353. [PubMed] [Google Scholar]
- Havlíček L, Hanuš J, Veselý J, Leclerc S, Meijer L, Shaw G, Strnad M. Cytokinin-derived cyclin-dependent kinase inhibitors: synthesis and cdc2 inhibitory activity of olomoucine and related compounds. Med Chem. 1997;40:408–412. doi: 10.1021/jm960666x. [DOI] [PubMed] [Google Scholar]
- Holý A. Isopolar phosphorus-modified nucleotide analogues. In: DeClercq E, editor. Advances in Antiviral Drug Design. Greenwich, CT: JAI Press, Inc.; 1994. pp. 179–232. [Google Scholar]
- Kirchhoff S, Kröger A, Cruz H, Tümmler M, Schäper F, Köster M, Hauser H. Regulation of cell growth by IRF-1 in BHK-21 cells. Cytotechnology. 1996;22:147–156. doi: 10.1007/BF00353934. [DOI] [PubMed] [Google Scholar]
- KováŐová H, Hajdúch M, Kořínková G, Halada P, Krupičková S, Gouldsworthy A, Zhelev N, Strnad M. Proteomics approach in classifying the biochemical basis of the anticancer activity of the new olomoucine-derived synthetic cyclindependent kinase inhibitor, bohemine. Electrophoresis. 2000;21:3757–3764. doi: 10.1002/1522-2683(200011)21:17<3757::AID-ELPS3757>3.0.CO;2-X. [DOI] [PubMed] [Google Scholar]
- Kramata P, Votruba I, Otová B, Holý A. Different inhibitory potencies of acyclic phosphonomethoxyalkyl nucleotide analogs toward DNA polymerases alpha, delta and epsilon. Mol Pharmacol. 1996;49:1005–1011. [PubMed] [Google Scholar]
- Kruh J. Effects of sodium butyrate, a new pharmacological agent, on cells in culture. Mol Cell Biochem. 1982;42:65–82. doi: 10.1007/BF00222695. [DOI] [PubMed] [Google Scholar]
- Legraverend M, Ludwig O, Bisagni E, Leclerc S, Meijer L, Giocanti N, Sadri R, Favaudon V. Synthesis and in vitro evaluation of novel 2,6,9-trisubstituted purines acting as cyclindependent kinase inhibitors. Bioorg Med Chem. 1999;7:1281–1293. doi: 10.1016/S0968-0896(99)00064-4. [DOI] [PubMed] [Google Scholar]
- Legraverend M, Tunnah P., Noble M, Ducrot P, Ludwig O, Grierson DS, Leost M, Meijer L, Endicott J. Cyclin-dependent kinase inhibition by new C-alkynylated purine derivatives and molecular structure of a CDK2-inhibitor complex. J Med Chem. 2000;43:1282–1292. doi: 10.1021/jm9911130. [DOI] [PubMed] [Google Scholar]
- Meijer L, Borgne A, Mulner O, Chong JPJ, Blow JJ, Inagaki N, Inagaki M, Delcros J-G, Moulinoux J-P. Biochemical and cellular effects of roscovitine, a potent and selective inhibitor of the cyclin-dependent kinases cdc2, cdk2 and cdk5. Eur J Biochem. 1997;243:527–536. doi: 10.1111/j.1432-1033.1997.t01-2-00527.x. [DOI] [PubMed] [Google Scholar]
- Otyepka M. K., Havlíček L, Siglerová V, Strnad M, Koča J. Docking-based development of purine-like inhibitors of cyclin-dependent kinase - 2. J Med Chem. 2000;43:2506–2513. doi: 10.1021/jm990506w. [DOI] [PubMed] [Google Scholar]
- Pines J. Cyclines and cyclin-dependent kinases: A biochemical view. Biochem J. 1995;308:697–711. doi: 10.1042/bj3080697. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rosania GR, Chang YT, Perez O, Sutherlin D, Dong H, Lockhart DJ, Schultz PG. Myoseverin, a microtubule-binding molecule with novel cellular effects. Nature Biotechnol. 2000;18:304–308. doi: 10.1038/73753. [DOI] [PubMed] [Google Scholar]
- Suzuki E, Ollis DF. Enhanced antibody production at slowed growth rates: Experimental demonstration and a structured model. Biotechnol Prog. 1990;6:231–236. doi: 10.1021/bp00003a013. [DOI] [PubMed] [Google Scholar]
- Suzuki E, Takahashi K, Ollis DF, et al. A simple structured model predicted positively-, negatively-, or non-growth associated antibody production rate depending on culture conditions. In: Murakami H, et al., editors. Animal Cell Technology: Basic and Applied Aspects. Dordrecht: Kluwer Academic Publishers; 1992. pp. 375–381. [Google Scholar]
- Takahashi K, Terada S, Ueda H, Makishima F, Suzuki E. Growth rate suppression of cultured animal cells enhances protein productivity. Cytotechnology. 1994;15:54–64. doi: 10.1007/BF00762379. [DOI] [PubMed] [Google Scholar]
- Veselý J, Havlíček L, Strnad M, Blow JJ, Donella-Deana A, Pinna L, Letham DS, Kato J, Detivaud L, Leclerc S. Inhibition of cyclin-dependent kinases by purine analogues. Eur J Biochem. 1994;224:771–786. doi: 10.1111/j.1432-1033.1994.00771.x. [DOI] [PubMed] [Google Scholar]
