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Sperm cells in pollen tubes ofNicotians tabacum L.: three-dimensional reconstruction, cytoplasmic diminution, and quantitative cytology

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Summary

The organization of the sperm cells and vegetative nucleus (male germ unit) ofNicotiana tabacum was examined 18 h after semivivo pollination using transmission electron microscopy, computerassisted serial section reconstruction and quantitative cytology. Based on a measurement of 11 cellular parameters in nine reconstructed sperm cell pairs, there are no statistically significant differences between the two cells. The Svn is characterized by a strapshaped cytoplasmic extension that is physically associated with the surface of the vegetative nucleus. The nucleus is located adjacent to the sperm crosswall, with sperm organelles being distributed between the nucleus and the extension. The Sua is a tapered cell with cytoplasmic areas at both poles and deep axial invaginations near the crosswall. This cell has a centrally-located nucleus and a largely polar distribution of organelles. Three mechanisms for cytoplasmic diminution were observed that appear to contribute actively to the loss of cytoplasmic volume and organelles: (1) enucleated cytoplasmic body production in the Sua; (2) vesiculation at the tip of the cytoplasmic projection of the Svn; and (3) vesicle-containing body accumulation in the periplasm of both the Svn and Sua.

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Abbreviations

3-D:

three-dimensional

ECB:

enucleated cytoplasmic body

MGU:

male germ unit

Svn :

leading sperm cell

Sua :

trailing sperm cell

TEM:

transmission electron microscopy

VCB:

vesicle-containing body

References

  • Cresti M, Lancelle SA, Hepler PK (1987) Structure of the generative cell wall complex after freeze substitution in pollen tubes ofNicotiana andImpatiens. J Cell Sci 88: 373–378

    Google Scholar 

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

    Google Scholar 

  • Galey FR, Nilsson SEG (1966) A new method for transferring sections from the liquid surface of the trough through staining solutions to the supporting film of a grid. J Ultrastruct Res 14: 405–410

    Google Scholar 

  • Hagemann R, Schröder MB (1989) The cytological basis of the plastid inheritance in angiosperms. Protoplasma 153: 57–64

    Google Scholar 

  • Heslop-Harrison J, Heslop-Harrison Y (1989) Myosin associated with the surfaces of organelles, vegetative nuclei and generative cells in angiosperm pollen grains and tubes. J Cell Sci 94: 319–325

    Google Scholar 

  • — —, Cresti M, Tiezzi A, Moscatelli A (1988) Cytoskeletal elements, cell shaping and movement in the angiosperm pollen tube. J Cell Sci 91: 49–60

    Google Scholar 

  • Hu SY, Yu HS (1988) Preliminary observations on the formation of the male germ unit in pollen tubes ofCyphomandra betacea Sendt. Protoplasma 147: 55–63

    Google Scholar 

  • McConchie CA, Hough T, Knox RB (1987 a) Ultrastructural analysis of the sperm cells of maize,Zea mays. Protoplasma 139: 9–19

    Google Scholar 

  • —, Russell SD, Durnas C, Tuohy M, Knox RB (1987 b) Quantitative cytology of the egg and central cellBrassica campestris andB oleracea. Planta 170: 446–452

    Google Scholar 

  • Medgyesy P, Páy A, Márton L (1986) Transmission of paternal chloroplasts inNicotiana. Mol Gen Genet 204: 195–198

    Google Scholar 

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

    Google Scholar 

  • Murgia M, Wilms HJ (1988) Three dimensional image and mitochondrial distribution in sperm cells ofEuphorbia dulcis. In: Wilms HJ, Keijzer CJ (eds) Plant sperm cells as tools for biotechnology. Pudoc, Wageningen, pp 75–80

    Google Scholar 

  • Provoost E, Southworth D, Knox RB (1988) Three-dimensional reconstruction of sperm cells and vegetative nucleus in pollen ofGerbera jamesonii. In: Wilms HJ, Keijzer CJ (eds) Plant sperm cells as tools for biotechnology. Pudoc, Wageningen, pp 69–74

    Google Scholar 

  • Roeckel P, Chaboud A, Matthys-Rochon E, Russell S, Dumas C (1990) Sperm cell structure, development and organization. In: Blackmore S, Knox RB (eds) Microspores: evolution and ontogeny. Academic Press, London, pp 281–307

    Google Scholar 

  • Rusche ML (1988) The male germ unit ofZea mays in the mature pollen grain. In: Wilms HJ, Keijzer CJ (eds) Plant sperm cells as tools for biotechnology. Pudoc, Wageningen, pp 61–68

    Google Scholar 

  • —, Mogensen HL (1988) The male germ unit ofZea mays: quantitative ultrastructure and three-dimensional analysis. In: Cresti M, Gori P, Pacini E (eds) Sexual reproduction in higher plants. Springer, Berlin Heidelberg New York Tokyo, pp 221–226

    Google Scholar 

  • Russell SD (1984) Ultrastructure of the sperm ofPlumbago zeylanica: 2. Quantitative cytology and three-dimensional reconstruction. Planta 162: 385–391

    Google Scholar 

  • — (1985) Preferential fusion inPlumbago zeylanica: ultrastructural evidence for gamete recognition in an angiosperm. Proc Natl Acad Sci USA 82: 6129–6134

    Google Scholar 

  • — (1990) A method for improved resolution for fluorescence microscopy using plastic-embedded material subjected to resin extraction. Stain Technol 64: 259–261

    Google Scholar 

  • —, Cass DD (1981) Ultrastructure of the sperm ofPlumbago zeylanica: 1. Cytology and association with the vegetative nucleus. Protoplasma 107: 85–107

    Google Scholar 

  • —, Yu HS (1991) Male cytoplasmic diminution in generative and sperm cells of flowering plants. Amer J Bot 78 [Suppl 6]: 34

    Google Scholar 

  • —, Rougier M, Dumas C (1990) Organization of the early postfertilization megagametophyte ofPopulus deltoides: ultrastructure and implications for male cytoplasmic transmission. Protoplasma 155: 153–165

    Google Scholar 

  • Taylor P, Kendrick J, Li Y, Gunning BES, Knox RB (1989) The male germ unit ofRhododendron: quantitative cytology, threedimensional reconstruction, isolation and detection using fluorescent probes. Sex Plant Reprod 2: 254–264

    Google Scholar 

  • Wagner VT, Mogensen HL (1988) The male germ unit in the pollen and pollen tubes ofPetunia hybrida: ultrastructural, quantitative and three-dimensional features. Protoplasma 143: 101–110

    Google Scholar 

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

    Google Scholar 

  • Young SJ, Royer SM, Groves PM, Kinnamon JC (1987) Threedimensional reconstructions from serial micrographs using the IBM PC. J Electron Microsc Tech 6: 207–218

    Google Scholar 

  • Yu HS, Hu SY, Zhu C (1989) Ultrastructure of sperm cells and the male germ unit ofNicotiana tabacum. Protoplasma 152: 29–36

    Google Scholar 

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Yu, H.S., Hu, S.Y. & Russell, S.D. Sperm cells in pollen tubes ofNicotians tabacum L.: three-dimensional reconstruction, cytoplasmic diminution, and quantitative cytology. Protoplasma 168, 172–183 (1992). https://doi.org/10.1007/BF01666263

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  • DOI: https://doi.org/10.1007/BF01666263

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