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The effects of ruthenium red, lanthanum, fluorescein isothiocyanate and trifluoperazine on vesicle transport, vesicle fusion and tip extension in pollen tubes

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Abstract

The effects of ruthenium red, lanthanum, fluorescein isothiocyanate and trifluoperazine, all antagonists of Ca2+ function in cells, have been studied in growing pollen tubes of Tradescantia virginiana. All four drugs inhibit pollen-tube growth but bring about different ultrastructural changes at the growing tips and within the cytoplasm. The results strongly support the hypothesis that Ca2+ plays a vital role in the mechanism of pollen-tube tip growth. The effect of ruthenium red provides evidence that sequestration of Ca2+ by mitochondria critically adjusts the concentration of these ions at tube tips. Fluorescein isothiocyanate appears to be a potent inhibitor of vesicle fusion at the plasma membrane, with vesicles accumulating in the tip at rates equivalent to those determined previously for their production. Both vesicle fusion and tip extension are regulated by Ca2+ but appear to be independently controlled processes.

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References

  • Ash, G.R., Bygrave, F.L. (1977) Ruthenium red as a probe in assessing the potential of mitochondria to control intracellular calcium in liver. FEBS Lett. 78, 166–168

    Google Scholar 

  • Brewbaker, J.L., Kwack, B.H. (1963) The essential role of calcium ion in pollen germination and pollen tube growth. Am. J. Bot. 50, 859–865

    Google Scholar 

  • Cheung, W.Y. (1980) Calmodulin plays a pivotal role in cellular regulation. Science 207, 19–27

    Google Scholar 

  • Dieter, P., Marmé, D. (1983) The effect of calmodulin and far red light on the kinetic properties of the mitochondrial and microsomal calcium-ion transport system from Corn. Planta 159, 277–281

    Google Scholar 

  • Fletcher, J.M., Greenfield, B.F., Hardy, C.J., Scargill, D., Woodhead, J.L. (1961) Ruthenium red. J. Chem. Soc. 2000–2006

  • Jaffe, L.A., Weisenseel, M.H., Jaffe, L.F. (1975) Calcium accumulations within the growing tips of pollen tubes. J. Cell Biol. 67, 488–492

    Google Scholar 

  • Klee, C.B., Crouch, T.H., Richman, P.G. (1980) Calmodulin. Annu. Rev. Biochem. 49, 489–515

    Google Scholar 

  • Kuroda, R., Kuroda, H. (1982) Relation of cytoplasmic calcium to contractibility in Physarum polycephalum. J. Cell. Sci. 53, 37–48

    Google Scholar 

  • Marmé, D., Dieter, P. (1983) The role of Ca2+ and calmodulin in plants. In: Calcium and cell function, vol. 4, pp. 263–311, Cheung, W.Y., ed. Academic Press, New York London

    Google Scholar 

  • Martin, R.B., Richardson, F.S. (1979) Lanthanides as probes for calcium in biological systems. Q. Rev. Biophys. 12, 181–209

    Google Scholar 

  • Mitchinson, C., Wilderspin, A.F., Trinnaman, B.J., Green, N.M. (1982) Identification of a labelled peptide after stoicheiometric reaction of fluorescein isothiocyanate with the Ca2+-dependent adenosine triphosphate of sarcoplasmic reticulum. FEBS Lett. 146, 87–92

    Google Scholar 

  • Morrè, D.J., Van der Woude, W.J. (1974) Origin and growth of cell surface components. In: Macromolecules regulating growth and development. 13th Symp. Soc. Devel. Biol., pp. 81–111, Hay, E.D., King, T.J., Papaconstantinou, J., eds. Academic Press, New York London

    Google Scholar 

  • Pick, U. (1981) Interaction of fluorescein isothiocyanate with nucleotide-binding sites of the Ca-ATPase from sarcoplasmic reticulum. Eur. J. Biochem. 121, 187–195

    Google Scholar 

  • Pick, U., Karlish, S.J.D. (1980) Indications for an oligomeric structure and for conformational changes in sarcoplasmic reticulum Ca2+-ATPase labelled selectively with fluorescein. Biochim. Biophys. Acta 626, 255–261

    Google Scholar 

  • Picton, J.M., Steer, M.W. (1981) Determination of secretory vesicle production rates by dictyosomes in pollen tubes of Tradescantia using cytochalasin D. J. Cell Sci. 49, 261–272

    Google Scholar 

  • Picton, J.M., Steer, M.W. (1982) A model for the mechanism of tip extension in pollen tubes. J. Theor. Biol. 98, 15–20

    Google Scholar 

  • Picton, J.M., Steer, M.W. (1983a) Evidence for the role of Ca2+ ions in tip extension in pollen tubes. Protoplasma 115, 11–17

    Google Scholar 

  • Picton, J.M., Steer, M.W. (1983b) Membrane recycling and the control of secretory activity in pollen tubes. J. Cell Sci. 63, 303–310

    Google Scholar 

  • Polito, V.S. (1983) Membrane-associated calcium during pollen grain germination: a microfluorometric analysis. Protoplasma 117, 226–232

    Google Scholar 

  • Pollard, T.D. (1981) Purification of a calcium-sensitive actin gelation protein from Acanthamoeba. J. Biol. Chem. 256, 7666–7670

    Google Scholar 

  • Reed, K.C., Bygrave, F.L. (1974) The inhibition of mitochondrial calcium transport by lanthanides and ruthenium red. Biochem. J 140, 143–155

    Google Scholar 

  • Reiss, H.-D., Herth, W. (1978) Visualization of Ca2+-gradient in growing pollen tubes of Lilium longiflorum with chlortetracycline. Protoplasma 97, 373–377

    Google Scholar 

  • Reiss, H.-D., Herth, W. (1979) Calcium ionophore A23187 affects localized wall secretion in tip region of pollen tubes of Lilium longiflorum. Planta 145, 225–232

    Google Scholar 

  • Rose, P.E. (1980) Improved tables for the evaluation of sphere size distribution including the effect of section thickness. J. Microsc. (Oxford) 118, 135–141

    Google Scholar 

  • Roufogalis, B.D., Minocherhomjee, A.-E.-V.M., Al-Jobore, A. (1983) Pharmacological antagonists of calmodulin. Can. J. Biochem. Cell Biol. 61, 927–933

    Google Scholar 

  • Shannon, T.M., Picton, J.M., Steer, M.W. (1984) The inhibition of dictyosome vesicle formation in higher plant cells by cytochalasin D. Eur. J. Cell Biol. 33, 144–147

    Google Scholar 

  • Steer, M.W., Picton, J.M. (1984) Control of cell wall formation in pollen tubes: the interaction of dictyosome activity with the rate of tip extension. In: Structure, function and metabolism of plant cell walls. Proc. 7th Annu. Symp. Bot., University of California, Riverside, Dugger, W. M., Bartnicki-Garcia, S., eds., pp. 483–494. Am. Soc. Plant Physiologists

  • Stossel, T.P. (1982) The structure of cortical cytoplasm. Philos. Trans. R. Soc. London Ser. B 299, 275–289

    Google Scholar 

  • Stossel, T.P., Hartwig, J.H., Yin, H.L. (1981) Actin gelation and the structure and movement of cortical cytoplasm. In: Cytoskeletal elements and plasma membrane organisation, pp. 139–168, Poste, G., Nicolson, G.L., eds. Elsevier/North-Holland Biomedical Press, Amsterdam New York Oxford

    Google Scholar 

  • Taylor, D.L., Fechheimer, M. (1982) Cytoplasmic structure and contractility: the solation — contraction coupling hypothesis. Philos. Trans. R. Soc. London Ser. B 299, 185–197

    Google Scholar 

  • Vasington, F.D., Gazzotti, P., Tiozzo, R., Carafoli, E. (1972) The effect of ruthenium red on Ca2+ transport and respiration in rat liver mitochondria. Biochim. Biophys. Acta 256, 43–54

    Google Scholar 

  • Yin, H.L., Zaner, K.S., Stossel, T.P. (1980) Interaction of gelsolin with actin filaments and regulation of actin gelation. J. Biol. Chem. 255, 9494–9500

    Google Scholar 

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Picton, J.M., Steer, M.W. The effects of ruthenium red, lanthanum, fluorescein isothiocyanate and trifluoperazine on vesicle transport, vesicle fusion and tip extension in pollen tubes. Planta 163, 20–26 (1985). https://doi.org/10.1007/BF00395892

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  • DOI: https://doi.org/10.1007/BF00395892

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