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The male germ unit of Rhododendron: quantitative cytology, three-dimensional reconstruction, isolation and detection using fluorescent probes

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Summary

The sperm cells of Rhododendron laetum and R. macgregoriae differentiate within the pollen tube about 24 h after germination in vitro. Threedimensional reconstruction shows that the sperm cells are paired together, and both have extensions that link with the tube nucleus, forming a male germ unit. Quantitative analysis shows that the sperm cells in each pair differ significantly in surface area, but not in cell volume nor in numbers of mitochondria or plastids. When isolated from pollen tubes by osmotic shock, the sperm cells became ellipsoidal and surrounded by their own plasma membrane, while a proportion remained in pairs linked by the inner tube plasma membrane. Both generative and sperm cells are visualized in pollen tube preparations by immunofluorescence with anti-tubulin and anti-actin monoclonal antibodies (MAbs) combined with H33258 fluorescence of the nuclei. Video-image processing shows the presence of an axial microtubule cage in the generative cells, and some microtubules are present in the cytoplasmic extensions that clasp the tube nucleus. Following sperm cell division, the extensive phragmoplast between the sperm nuclei is partitioned by the plasma membranes.

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References

  • Brewbaker JL, Kwack BY (1963) The essential role of calcium in pollen germination and tube growth. Am J Bot 50:859–865

    CAS  Google Scholar 

  • Coleman AW, Maguire M, Coleman JR (1981) Mithramycin and 4′,6′-diamidino-2-phenylindole (DAPI) staining for fluorescence microspectrophotometric measurement of DNA in nuclei, plastids and virus particles. J Histochem Cytochem 29:959–968

    Google Scholar 

  • Cresti M, Ciampolini F, Kapil RN (1984) Generative cells of some angiosperms with particular emphasis on their microtubules. J Submicrosc Cytol 16:317–326

    Google Scholar 

  • Derksen J, Pierson ES, Traas JA (1985) Microtubules in vegetative and generative cells of pollen tubes. Eur J Cell Biol 38:112–118

    Google Scholar 

  • Dumas C, Knox RB, McConchie CA, Russell SD (1984) Emerging physiological concepts in fertilization. What's New In Plant Physiol 15:17–20

    Google Scholar 

  • Franke W, Herth W, Woude W van der, Morre D (1972) Tubular and filamentous structures in pollen tubes: possible involvement as guide elements in protoplasmic streaming and vectorial migration of secretory vesicles. Planta 105:317–341

    Google Scholar 

  • Heslop-Harrison J (1988) The pollen tube: motility and cytoskeleton. In: Cresti M, Gori P, Pacini E (eds) Sexual reproduction in higher plants. Springer, Berlin Heidelberg New York pp 195–203

    Google Scholar 

  • Heslop-Harrison J, Heslop-Harrison Y, Cresti M, Tiezzi A, Moscatelli A (1988) Cytoskeletal elements, cell shaping and movement in the angiosperm pollen tube. J Cell Sci 91:44–60

    Google Scholar 

  • Hough T, Singh MB, Smart IJ, Knox RB (1986) Immunofluorescent screening of monoclonal antibodies to surface antigens of animal and plant cells bound to polycarbonate membranes. J Immunol Methods 92:103–107

    Google Scholar 

  • Hu S, Zhu C, Xu L (1981) Ultrastructure of male gametophyte in wheat. II. Formation and development of sperm cell. Acta Bot Sin 23:87–91

    Google Scholar 

  • Kaul V, Theunis CH, Palser BF, Knox RB, Williams EG (1987) Association of the generative cell and vegetative nucleus in pollen tubes of Rhododendron. Ann Bot (London) 59:227–235

    Google Scholar 

  • Knox RB, Southworth D, Singh MB (1988) Sperm cell determinants and control of fertilisation in plants. In: Chapman GP, Ainsworth CC, Chatham CJ (eds) Eukaryote cell recognition. Concepts and model systems. Cambridge University Press, Cambridge, pp 175–193

    Google Scholar 

  • Lin J, Uwate WJ, Stallman V (1977) Ultrastructural localization of acid phosphatase in pollen tube of Primus avium L. (sweet cherry). Planta 135:183–190

    Google Scholar 

  • Maheshwari P (1950) An introduction to the embryology of angiosperms. McGraw-Hill, New York

    Google Scholar 

  • Marc J, Gunning BES (1986) Immunofluorescent localization of cytoskeletal tubulin and actin during spermatogenesis in Pteridium aquilinum (L.) Kuhn. Protoplasma 134:163–177

    Google Scholar 

  • Marc J, Gunning BES (1988) Monoclonal antibodies to a fern spermatozoid detect novel components of the mitotic and cytokinetic apparatus in higher plant cells. Protoplasma 142:15–24

    Google Scholar 

  • Marc J, Gunning BES, Hardham AR, Perkin JL, Wick SM (1988) Monoclonal antibodies to surface and cytoskeletal components of the spermatozoid of Pteridium aquilinum. Protoplasma 142:5–14

    Google Scholar 

  • McConchie CA, Jobson S, Knox RB (1985) Computer-assisted reconstruction of the male germ unit in pollen of Brassica campes tris. Protoplasma 127:57–63

    Google Scholar 

  • McConchie CA, Russell SD, Dumas C, Tuohy M, Knox RB (1987) Quantitative cytology of the sperm cells of Brassica campestris and B. oleracea. Planta 170:446–452

    Google Scholar 

  • Mogensen HL, Rusche ML (1985) Quantitative ultrastructural analysis of barley sperm. I. Occurrence and mechanism of cytoplasm and organelle reduction and the question of sperm dimorphism. Protoplasma 128:1–13

    Google Scholar 

  • Palevitz BA, Cresti M (1988) Microtubule organization in the sperm of Tradescantia virginiana. Protoplasma 146:28–34

    Google Scholar 

  • Pierson ES, Derksen J, Traas JA (1986) Organization of microfilaments and microtubules in pollen tubes grown in vitro or in vivo in various angiosperms. Eur J Cell Biol 41:14–18

    Google Scholar 

  • Raudaskoski M, Astrom H, Perttila K, Virtanen I, Louhelainen J (1987) Role of the microtubule cytoskeleton in pollen tubes: an immunocytochemical and ultrastructural approach. Biol Cell 61:177–188

    Google Scholar 

  • Russell SD (1984) Ultrastructure of the sperm of Plumbago zeylanica. II. Quantitative cytology and three-dimensional organization. Planta 162:385–391

    Google Scholar 

  • Russell SD (1985) Preferential fertilization on Plumbago: ultrastructural evidence for gamete level recognition in an angiosperm. Proc Natl Acad Sci USA 82:6129–6132

    Google Scholar 

  • Russell SD, Cass DD (1983) Unequal distribution of plastids and mitochondria during sperm cell formation in Plumbago zeylanica. In: Mulcahy DL, Ottaviano E (eds) Pollen. Biology and implications for plant breeding. Elsevier, Amsterdam New York, pp 135–140

    Google Scholar 

  • Shivanna KR, Xu H, Taylor P, Knox RB (1988) Isolation of sperms from the pollen tubes of flowering plants during fertilization. Plant Physiol 87:647–650

    Google Scholar 

  • Spurr A (1969) A low viscosity epoxy resin embedding medium for electron microscopy. J Ultrastruct Res 26:31–43

    CAS  PubMed  Google Scholar 

  • Staff IA, Taylor P, Kenrick J, Knox RB (1989) Ultrastructural analysis of plastids in angiosperm pollen tubes. Sex Plant Reprod 2:70–76

    Google Scholar 

  • Theunis CA, McConchie CA, Knox RB (1985) Three-dimensional reconstruction of the generative cell and its wall connection in mature bicellular pollen of Rhododendron. Micron Microsc Acta 16:225–231

    Google Scholar 

  • Tiezzi A, Cresti M, Ciampolini F (1986) Microtubules in Nicotiana pollen tubes: ultrastructural, immunofluorescence and biochemical data. In: Cresti M, Dallai R (eds) Biology of reproduction and cell motility in plants and animals. University of Siena, Siena pp 87–94

    Google Scholar 

  • Tiezzi A, Moscatelli A, Ciampolini F, Milanesi C, Murgia M, Cresti M (1988) The cytoskeletal apparatus of the generative cell in several angiosperm species. In: Cresti M, Gori P, Pacini E (eds) Sexual reproduction in higher plants. Springer, Berlin Heidelberg New York, pp 215–220

    Google Scholar 

  • Tilney-Bassett RAE (1978) The inheritance and genetic behaviour of plastids. In: Kirk J, Kirk D, Tilney-Bassett RAE (eds) The plastid. Elsevier/North Holland, Amsterdam New York, pp 251–524

    Google Scholar 

  • Williams EG, Ramm-Anderson S, Dumas C, Mau S, Clarke AE (1982) The effect of isolated components of Prunus avium L. styles on in vitro growth of pollen tubes. Planta 156:517–519

    Google Scholar 

  • Wilms HJ (1986) Dimorphic sperm cells in the pollen grain of Spinacia. In: Cresti M, Dallai R (eds) Biology of reproduction and motility in plants and animals, University of Siena, Siena, pp 193–198

    Google Scholar 

  • Wilms HJ, Van Aelst AC (1983) Ultrastructure of spinach sperm cells in mature pollen. In: Erdelska O (ed) Fertilization and embryogenesis in ovulated plants, Czech Centre Biol Ecol Sci, Bratislava, pp 105–112

    Google Scholar 

  • Wilms HJ, Leferink-ten Klooster HB (1983) Ultrastructural changes of spinach sperm cells during the progamic phase. Czech Centre Biol Ecol Sci, Bratislava, pp 239–240

    Google Scholar 

  • Zhu C, Hu S, Xu L, Li X, Shen J (1980) Ultrastructure of sperm cell in mature pollen grain of wheat. Sci Sin 23:371–376

    Google Scholar 

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Taylor, P., Kenrick, J., Li, Y. et al. The male germ unit of Rhododendron: quantitative cytology, three-dimensional reconstruction, isolation and detection using fluorescent probes. Sexual Plant Reprod 2, 254–264 (1989). https://doi.org/10.1007/BF00195585

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