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Centrosome and microtubule dynamics in apical cells ofSphacelaria rigidula (Phaeophyceae) treated with nocodazole

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Summary

Treatment of young thalli ofSphacelaria rigidula with 0.04 μg of nocodazole (Nz) per ml for up to 36 h affects microtubules (Mts) only slightly, but blocks a large number of mitotic cells in metaphase, without disruption of the metaphase plate. Higher concentrations of Nz (0.1 μg/ml) depolymerize interphase Mts. Only a few perinuclear and some short Mts resist and remain associated with the centrosomes. Fragmented Mts or groups of Mts sometimes remain in the apical dome. After treatment with 0.1 μg of Nz per ml, prometaphase cells are blocked at metaphase, while post-metaphase cells become binuclear, due to the failure of cytokinesis. With anticentrin immunofluorescence, a positive centrin signal is always observed in the centrosome area. Centrosome duplication is not affected by Nz, but separation is disturbed. After recovering for 2–4 h, most of the blocked metaphases proceed normally. In such cells duplicated centrosomes are seen in different stages of separation. In some cells independent aster-like microtubule configurations appear in the apical dome, occasionally displaying centrin at their centre. During recovery various configurations of bimitosis or multipolar mitosis were found. The multipolar spindles may share common centrosomes. Up to four centrosomes may accompany each nucleus. In some 24 h treated cells, as well as in cells recovering for 2 h, the centrin-positive structure is rod-like, extending in opposite directions from the usual position to the poles. Electron microscopical examination of thin sections revealed that the growth pattern of the apical cells is disrupted after Nz treatment. The observations show that: (a) the Mt cytoskeleton is involved in maintaining the polarity and growth pattern of apical cells, (b) mitosis is blocked by low concentrations of Nz without significant depolymerization of Mts, (c) the centrosome cycle is independent of the nuclear cycle, (d) centrosome separation and differentiation are disturbed by Nz treatment, (e) during recovery from Nz treatment, centrosomal material that may have separated from the centrosomes, as well as Mt fragments that resisted depolymerization, may operate as Mt nucleation centres.

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Abbreviations

DIC:

differential interference contrast

EM:

electron microscope

Mt:

microtubule

MTOC:

microtubule-organizing center

Nz:

nocodazole

NBBC:

nucleus-basal body connector

References

  • Alieva IB, Vorobjev IA (1991) Induction of multipolar mitoses in cultured cells: decay and restructuring of the mitotic apparatus and distribution of centrioles. Chromosoma 100: 532–542

    Google Scholar 

  • Allen VW, Kropf DL (1992) Nuclear rotation and lineage specification inPelvetia embryos. Development 115: 873–883

    Google Scholar 

  • Bajer AS, Molé-Bajer J (1972) Spindle dynamics and chromosome movements. Int Rev Cytol Suppl 3: 1–271

    Google Scholar 

  • Balczon R (1996) The centrosome in animal cells and its functional homologs in plant and yeast cells. Int Rev Cytol 169: 25–82

    Google Scholar 

  • Baron AT, Salisbury JL (1992) Role of centrin in spindle pole dynamics. In: Kalmins VI (ed) The centrosomes. Academic Press, San Diego, pp 331–351

    Google Scholar 

  • Brinkley BR (1985) Microtubule organizing centers. Annu Rev Cell Biol 1: 145–172

    Google Scholar 

  • Brawley SH, Quatrano RS (1979) Effects of microtubule inhibitors on pronuclear migration and embryogenesis inFucus distichus (Phaeophyta). J Phycol 15: 266–272

    Google Scholar 

  • Chen R-H, Waters J, Salmon ED, Murray AW (1996) Association of spindle assembly checkpoint component XMAD2 with unattached kinetochores. Science 274: 242–246

    Google Scholar 

  • Clayton L, Lloyd CW (1984) The relationship between the division plane and spindle geometry inAllium cells treated with CIPC and griseofulvin: an antitubulin study. Eur J Cell Biol 34: 248–253

    Google Scholar 

  • Cyr RJ, Palevitz BA (1995) Organization of cortical microtubules in plant cells. Curr Opin Cell Biol 7: 65–71

    Google Scholar 

  • De Brabander M, Van de Veire RML, Aerts FEM, Borges M, Janssen PAJ (1976) The effects of [5-(2-thienylcarbonyl)-1H-benzimidazol-2-yl)] carbamate (R17934; NSC 238159), a new synthetic antitumoral drug interfering with microtubules, on mammalian cells cultured in vitro. Cancer Res. 36: 905–916

    Google Scholar 

  • Derksen J, Emons AM (1990) Microtubules in tip growth systems. In: Heath IB (ed) Tip growth in plant and fungal cells. Academic Press, New York, pp 147–181

    Google Scholar 

  • Doonan JH, Duckett JG (1988) The bryophyte cytoskeleton: experimental and immunofluorescence studies of morphogenesis. Adv Bryol 3: 1–31

    Google Scholar 

  • —, Cove DJ, Lloyd CW (1985) Immunofluorescence microscopy of microtubules in intact cell lineages of the moss,Physcomitrella patens. I. Normal and CIPC treated cells. J Cell Sci 75: 131–147

    Google Scholar 

  • — — — (1988) Microtubules and microfilaments in tip-growth: evidence that microtubules impose polarity on protonemal growth inPhyscomitrella patens. J Cell Sci 89: 533–540

    Google Scholar 

  • Hardwick RG, Murray AW (1995) Madlp, a phosphoprotein component of the spindle assembly checkpoint in budding yeast. J Cell Biol 131: 709–720

    Google Scholar 

  • Heath IB (ed) (1990) Tip growth in plant and fungal cells. Academic Press, New York

    Google Scholar 

  • Jordan MA, Thrower D, Wilson L (1991) Mechanism of inhibition of cell proliferation byVinca alcaloids. Cancer Res 51: 2212–2222

    Google Scholar 

  • — — — (1992) Effects of vinblastine, podophyllotoxin and nocodazole on mitotic spindles: implications for the role of microtubule dynamics in mitosis. J Cell Sci 102: 401–416

    Google Scholar 

  • Joshi C, Palevitz BA (1996) γ-Tubulin and microtubule organization in plants. Trends Cell Biol 6: 41–44

    Google Scholar 

  • Katsaros C (1980) An ultrastructural study on the morphogenesis of the thallus of five brown algal species. PhD thesis. University of Athens, Athens, Greece

    Google Scholar 

  • — (1992) Immunofluorescence study of microtubule organization in some polarized cell types of selected brown algae. Bot Acta 105: 400–406

    Google Scholar 

  • — (1995) Apical cells of brown algae, with particular reference to Sphacelariales, Dictyotales and Fucales. Phycol Res 43: 43–59

    Google Scholar 

  • —, Galatis B (1990) Thallus development inHalopteris filicina (Phaeophyceae, Sphacelariales). Br Phycol J 25: 63–74

    Google Scholar 

  • — — (1992) Immunofluorescence and electron microscope studies of microtubule organization during the cell cycle ofDictyota dichotoma (Phaeophyta, Dictyotales). Protoplasma 169: 75–84

    Google Scholar 

  • — —, Mitrakos K (1983) Fine structural studies on the interphase and dividing apical cells ofSphacelaria tribuloides (Phaeophyta). J Phycol 19: 16–30

    Google Scholar 

  • —, Kreimer G, Melkonian M (1991) Localization of tubulin and a centrin homologue in vegetative cells and developing gametangia ofEctocarpus siliculosus (Dillw.) Lyngb. (Phaeophyceae, Ectocarpales): a combined immunofluorescence and confocal laser scanning microscope study. Bot Acta 104: 87–92

    Google Scholar 

  • —, Maier I, Melkonian M (1993) Immunolocalization of centrin in the flagellar apparatus of male gametes ofEctocarpus siliculosus (Phaeophyceae) and other brown algal motile cells. J Phycol 29: 787–797

    Google Scholar 

  • Karyophyllis D, Galatis B, Katsaros C (1996) Centrosome and microtubule dynamics in apical cells ofSphacelaria rigidula treated with nocodazole. In: Abstracts of the 1st European Phycological Congress, Cologne. Cambridge University Press, Cambridge, p 36

    Google Scholar 

  • Keryer G, Ris H, Borisy GG (1984) Centriole distribution during tripolar mitosis in chinese hamster ovary cells. J Cell Biol 98: 2222–2229

    Google Scholar 

  • Kropf DL (1992) Establishment and expression of cellular polarity in fucoid zygotes. Microbiol Rev 56: 316–339

    Google Scholar 

  • — (1994) Cytoskeletal control of cell polarity in a plant zygote. Dev Biol 165: 361–371

    Google Scholar 

  • —, Maddock A, Gard DL (1990) Microtubule distribution in earlyPelvetia development. J Cell Sci 97: 545–552

    Google Scholar 

  • Lambert A-M (1993) Microtubule-organizing centers in higher plants. Curr Opin Cell Biol 5: 116–122

    Google Scholar 

  • —, Vantard M, Schmit A-C, Stoeckel H (1991) Mitosis in plants. In: Lloyd CW (ed) The cytoskeletal basis in plant growth and form. Academic Press, London, pp 199–208

    Google Scholar 

  • Li Y, Benezia R (1996) Identification of a human mitotic checkpoint gene: hsMAD2. Science 274: 246–248

    Google Scholar 

  • Mazia D (1984) Centrosomes and mitotic poles. Exp Cell Res 153: 1–15

    Google Scholar 

  • — (1987) The chromosome cycle and the centrosome cycle in the mitotic cycle. Int Rev Cytol 100: 49–92

    Google Scholar 

  • Melkonian M, Beech PL, Katsaros C, Schulze D (1991) Centrinmediated cell motility in algae. In: Melkonian M (ed) Algal cell motility. Chapman and Hall, New York, pp 192–217

    Google Scholar 

  • Menzel D (1992) Cell architecture and cellular morphogenesis of eukaryotic algae (Rhodophyta and Phaeophyta). Prog Bot 54: 30–62

    Google Scholar 

  • Morejohn LC (1991) The molecular pharmacology of plant tubulin and microtubules. In: Lloyd CW (ed) The cytoskeletal basis in plant growth and form. Academic Press, London, pp 29–43

    Google Scholar 

  • Palevitz BA (1988) Microtubular fir-trees in mitotic spindles of onion roots. Protoplasma 142: 74–78

    Google Scholar 

  • Palmer RE, Sullivan DS, Huftaker T, Koshland D (1992) Role of astral microtubules and actin in spindle orientation and migration in the budding yeast,Saccharomyces cerevisiae. J Cell Biol 119: 583–593

    Google Scholar 

  • Provasoli L (1968) Media and prospects for the cultivation of marine algae. In: Watanabe A, Hattori A (eds) Cultures and collections of algae. Proceedings U.S.-Japan Conference 1966, Hakone. Japanese Society for Plant Physiologists, Kyoto, pp 63–75

    Google Scholar 

  • Raudaskoski M, Mao W-Z, Yli-Matila T (1994) Microtubule cytoskeleton in hyphal growth: response to nocodazole in a sensitive and a tolerant strain of the homobasidiomyceteSchizophyllum commune.. Eur J Cell Biol 64: 131–141

    Google Scholar 

  • Roberson RW, Vargas MM (1994) The tubulin cytoskeleton and its nucleation in hyphal tips ofAllomyces macrogynus. Protoplasma 182: 19–31

    Google Scholar 

  • Rupes I, Mao W-Z, Åström H, Raudaskoski M (1995) Effects of nocodazole and brefeldin A on microtubule cytoskeleton and membrane organization in the homobasidiomyceteSchizophyllum commune. Protoplasma 185: 212–221

    Google Scholar 

  • Rusig AM, Le Guyader H, Ducreux G (1993) Microtubule organization in the apical cell ofSphacelaria (Phaeophyceae) and its related protoplast. Hydrobiologia 260/261: 167–172

    Google Scholar 

  • — — — (1994) Dedifferentiation and microtubule reorganization in the apical cell protoplast ofSphacelaria (Phaeophyceae). Protoplasma 179: 83–94

    Google Scholar 

  • Salisbury JL (1995) Centrin, centrosomes, and mitotic spindles. Curr Opin Cell Biol 7: 39–15

    Google Scholar 

  • —, Baron AT, Surek B, Melkonian M (1984) Striated flagellar roots: isolation and partial characterization of a calcium-modulated contractile organelle. J Cell Biol 99: 962–970

    Google Scholar 

  • —, Sanders MA, Harpst L (1987) Flagellar root contraction and nuclear movement during flagellar regeneration inChlamydomonas reinhardtii. J Cell Biol 107: 635–641

    Google Scholar 

  • Schliwa M (1992) Cell polarity and centrosomes. In: Kalmins VI (ed) The centrosomes. Academic Press, San Diego, pp 331–351

    Google Scholar 

  • Sellitto C, Kuriyama R (1988) Distribution of pericentriolar material in multipolar spindles induced by colcemid treatment in Chinese hamster ovary cells. J Cell Sci 89: 57–65

    Google Scholar 

  • Sluiman H (1993) Nucleus, nuclear division and cell division. In: Berner T (ed) Ultrastructure of microalgae. CRC Press, Boca Raton, pp 221–255

    Google Scholar 

  • Smirnova EA, Bajer AS (1992) Spindle poles in higher plant mitosis. Cell Motil Cytoskeleton 23: 1–7

    Google Scholar 

  • Strone S (1993) Determination of cleavage planes. Cell 72: 3–6

    Google Scholar 

  • Van Beneden E (1883) Recherches sur la maturation de l'oeuf, la decondation et la division cellule. Arch Biol 4: 265–683

    Google Scholar 

  • Vorobjev IA, Nadezhdina ES (1987) The centrosome and its role in the organization of the microtubules. Int Rev Cytol 106: 227–293

    Google Scholar 

  • Wick SM (1985) Immunofluorescence microscopy of tubulin and microtubule array in plant cells. III. Transition between mitotic/cytokinetic and interphase microtubule arrays. Cell Biol Int Rep 9: 357–371

    Google Scholar 

  • Wright RL, Salisbury JL, Jarvik (1985) A nucleus-basal body connector inChlamydomonas reinhardtii that may function in basal body localization or segregation. J Cell Biol 101: 1903–1912

    Google Scholar 

  • Zieve GW, Turnbull D, Mullins JM, McIntosh JR (1980) Production of large numbers of mitotic cells by use of the reversible microtubule inhibitor nocodazole. Exp Cell Res 126: 397–405

    Google Scholar 

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Correspondence to C. Katsaros.

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Karyophyllis, D., Galatis, B. & Katsaros, C. Centrosome and microtubule dynamics in apical cells ofSphacelaria rigidula (Phaeophyceae) treated with nocodazole. Protoplasma 199, 161–172 (1997). https://doi.org/10.1007/BF01294504

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  • DOI: https://doi.org/10.1007/BF01294504

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