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Development of the model of cell cycle synchronization in early embryos of Danio rerio (Teleostei)

  • Cell Differentiation and Proliferation
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Abstract

An attempt was undertaken to develop a model system based on artificial cell cycle synchronization by means of reversible mitosis blocking in zebrafish embryos for studying the role of cell cycle synchrony in embryogenesis. Dechorionized and intact embryos at the stages of 512-cell blastula and 75% epiboly were treated with nocodazole and then washed within several times of exposure. When working on dechorionized embryos, we succeeded to obtain complete block mitosis in the presence of low nocodazole concentrations: 0.5–1.0 μg/ml. Block of mitosis was relieved in all experimental series within a certain time after the beginning of washing. This inertia depended on both nocodazole concentration and duration of treatment. The nocodazole elimination was significantly accelerated only after five (or more) changes of washing medium containing DMSO. As a result, the conditions were established for obtaining a parasynchronous cell population in the zebrafish gastrulas with a peak of mitosis up to 17.2%.

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References

  • Adams, R., Metody kul’tury kletok dlya biokhimikov (Methods of Cell Culture for Biochemists), Moscow: Mir, 1983.

    Google Scholar 

  • El Ali, M.Sh., Effect of Colchamine on Segmentation of Paraxial Mesoderm in Chick Embryo, Cand. Sci. (Biol.) Dissertation, St. Petersburg: SPbGU, 1993.

    Google Scholar 

  • Atés, Y. and Sentein, P., Action of Nocodazole on Segmentation Mitoses of Triturus helveticus Raz. Electron Microscopy, Biol. Cells, 1981, vol. 40, pp. 175–180.

    Google Scholar 

  • Baumann, M. and Sander, K., Bipartite Axiation Follows Incomplete Epiboly in Zebrafish Embryos Treated with Chemical Teratogens, J. Exp. Zool., 1984, vol. 230, pp. 363–376.

    Article  PubMed  CAS  Google Scholar 

  • Cleaver, J.E., Thymidine Metabolism and Cell Kinetics, Amsterdam: North Holland Publ. Co, 1967.

    Google Scholar 

  • De Brabander, M.J., Van de Veire, R.M.L., Aerts, F.E.M., et al., The Effects of Methyl [5-(2-Thienylcarbonyl)-1H-Benzimidzol-2-yl]Carbamate, (R 17934; NSC 238159), a New Synthetic Antitumoral Drug Interfering with Microtubules, on Mammalian Cells Culture in Vitro, Cancer Res., 1976, vol. 36, pp. 905–916.

    PubMed  Google Scholar 

  • Dondua, A.K. and Fedorova, Zh.E., Mitotic Cycles during Formation of Neural Tube and Somites in Chick Embryo under Culture Conditions, Issledovaniya kletochnykh tsiklov i metabolizma nukleinovykh kislot pri differentsiatsii kletok (Studies of Cell Cycles and Nucleic Acid Metabolism during Cell Differentiation), Moscow: Nauka, 1964, pp. 83–89.

    Google Scholar 

  • Dondua, A.K., Cell Cycles in Early Animal Development, Kletochnoe razmnozhenie i protsessy differentsirovki (Cell Proliferation and Differentiation), Moscow: Nauka, 1983, pp. 6–75.

    Google Scholar 

  • Emanuelsson, H., Mitotic Activity in Chick Embryos at the Primitive Streak Stage, Acta Physiol. Scand., 1961, vol. 52, pp. 211–233.

    PubMed  CAS  Google Scholar 

  • Foe, V.E., Mitotic Doamins Reveal Early Commitment of Cells of Drosophila Embryos, Development, 1989, vol. 107, pp. 1–22.

    PubMed  CAS  Google Scholar 

  • Kane, D.A. and Kimmel, C.B., The Zebrafish Midblastula Transition, Devel. Biol., 1993, vol. 119, pp. 447–456.

    CAS  Google Scholar 

  • Kato, Y. and Tsunoda, Y., Synchronous Division of Mouse Two-Cell Embryos with Nocodazole in Vitro, J. Reprod. Fertil., 1992, vol. 95, pp. 39–43.

    Article  PubMed  CAS  Google Scholar 

  • Kimmel, C.B., Ballard, W.W., and Kimmel, S.R., Stages of Embryonic Development of the Zebrafish, Devel. Dynamics, 1995, vol. 203, pp. 253–310.

    CAS  Google Scholar 

  • Mareel, M., Bellairs, R., De Bruyne, G., and Van Peteghem, M.C., Effect of Microtubule Inhibitors on the Expansion of Hypoblast and Margin of Overgrowth of Chick Blastoderm S, J. Embryol. Exp. Morphol., 1984, vol. 81, pp. 273–286.

    PubMed  CAS  Google Scholar 

  • Neyfakh, A.A. and Rott, N.N., Synchronization of Cell Division in Early Embryos of the Loach Misgurnus fossilis L. by Elevated Temperature, Dokl. Akad. Nauk. SSSR, 1958, vol. 119, no. 2, pp. 432–434.

    Google Scholar 

  • Neyfakh, A.A., Application of the Method of Radiation Inactivation of the Nuclei for Studying Their Function in Early Development of Fish, Zh. Obshch. Biol., 1959, vol. 20, no. 3, pp. 202–213.

    Google Scholar 

  • Neyfakh, A.A., Comparative Radiation Studies of Nuclear Morphogenetic Function in Animal Development, Zh. Obshch. Biol., 1961, vol. 22, no. 1, pp. 42–57.

    Google Scholar 

  • Newport, J. and Kirschner, M., A Major Developmental Transition in Early Xenopus Embryos. 1. Characterization and Timing of Cellular Changes at the Midblastula Stage, Cell, 1982, vol. 30, no. 3, pp. 675–686.

    Article  PubMed  CAS  Google Scholar 

  • Puck, T.T. and Steffen, J., Life Cycle Analysis of Mammalian Cells. 1. A Method for Localizing Metabolic Events within Cell Cycle and Its Application to the Action of Colcemide and Sublethal Doese of X-Irradiation, Biophys. J., 1963, vol. 3, pp. 379–389.

    Article  PubMed  CAS  Google Scholar 

  • Rieder, C.L. and Palazzo, R.E., Colcemid and Mitotic Cycle, J. Cell Sci., 1992, vol. 102, pp. 387–392.

    PubMed  CAS  Google Scholar 

  • Rott, N.N., Kletochnye tsikly v rannem embriogeneze zhivotnykh (Cell Cycles in Early Animal Development), Moscow: Nauka, 1987.

    Google Scholar 

  • Satoh, N., “Metachronous” Cleavage and Initiation of Gastrulation in Amphibian Embryos, Devel. Growth Differ., 1977, vol. 19, no. 2, pp. 111–117.

    Article  Google Scholar 

  • Solnica-Krezel, L. and Driever, W., Microtubule Arrays Function during Epiboly, Development, 1994, vol. 120, pp. 2443–2455.

    PubMed  CAS  Google Scholar 

  • Strahle, U. and Jesuthasan, S., Ultraviolet Irradiation Impairs Epiboly in Zebrafish Embryos: Evidence for a Microtubule-Dependent Mechanism of Epiboly, Devel. Biol., 1993, vol. 119, pp. 909–919.

    CAS  Google Scholar 

  • Taylor, E.W., The Mechanism of Colchicine Inhibition of Mitosis. 1. Kinetics of Inhibition and the Binding of H3-Colchicine, J. Cell Biol., 1965, vol. 25, no. 1, pp. 145–160.

    Article  PubMed  CAS  Google Scholar 

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Correspondence to V. I. Efremov.

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Original Russian Text © V.I. Efremov, G.M. Gluzdikova, E.V. Mukhachev, 2007, published in Ontogenez, 2007, Vol. 38, No. 5, pp. 372–379.

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Efremov, V.I., Gluzdikova, G.M. & Mukhachev, E.V. Development of the model of cell cycle synchronization in early embryos of Danio rerio (Teleostei). Russ J Dev Biol 38, 310–316 (2007). https://doi.org/10.1134/S1062360407050050

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  • DOI: https://doi.org/10.1134/S1062360407050050

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