Skip to main content
Log in

The wall ofPinus sylvestris L. pollen tubes

  • Published:
Protoplasma Aims and scope Submit manuscript

Summary

The wall ofPinus sylvestris pollen and pollen tubes was studied by electron microscopy after both rapid-freeze fixation and freeze-substitution (RF-FS) and chemical fixation. Fluorescent probes and antibodies (JIM7 and JIM5) were used to study the distribution of esterified pectin, acidic pectin and callose. The wall texture was studied on shadow-casted whole mounts of pollen tubes after extraction of the wall matrix. The results were compared to current data of angiosperms. TheP. sylvestris pollen wall consists of a sculptured and a nonsculptured exine. The intine consists of a striated outer layer, that stretches partly over the pollen tube wall at the germination side, and a striated inner layer, which is continuous with the pollen tube wall and is likely to be partly deposited after germination. Variable amounts of callose are present in the entire intine. No esterified pectin is detected in the intine and acidic pectin is present in the outer intine layer only. The wall of the antheridial cell contains callose, but no pectin is detectable. The wall between antheridial and tube cell contains numerous plasmodesmata and is bordered by coated pits, indicating intensive communication with the tube cell. Callose and esterified pectin are present in the tip and the younger parts of the pollen tubes, but both ultimately disappear from the tube. Sometimes traces in the form of bands remain present. No acidic pectin is detected in either tip or tube. The wall of the pollen tube tip has a homogenous appearance, but gradually attains a fibrillar character at aging, perhaps because of the disappearance of callose and pectin. No secondary wall formation or callose lining can be seen wilh the electron microscope. The densily of the cellulose microfibrils (CMF) is much lower in the tip than in the tube. Both show CMF in all but axial and nontransverse orientations. In conclusion,P. sylvestris and angiosperm pollen tubes share the presence of esterified pectin in the tip, the oblique orientations of the CMF, and the gradual differentiation of the pollen tube wall, indicating a possible relation to tip growth. The presence of acidic pectin and the deposition of a secondary-wall or callose layer in angiosperms but not inP. sylvestris indicales that these characteristics are not related to tip growth, but probably represent adaptations to the fast and intrastylar growth of angiosperms.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Abbreviations

CMF:

cellulose microfibrils

II:

inner intine

NE:

nonsculptured exine

OI:

outer intine

RF-FS:

rapid-freeze fixation freeze-substitution

SE:

sculptured exine

SER:

smooth endoplasmic reliculum

SV:

secretory vesicles

References

  • Ciampolini F, Li Y-Q, Cresti M, Calzoni GL, Speranza A (1993) Disorganization of dictyosomes by monensin treatment of in vitro germinated pollen ofMalus domestica Bork. Acta Bot Neerl 42: 349–356

    Google Scholar 

  • Dashek WV (1966) The lily pollen tube: aspects of fine chemistry and nutrition in relation to fine structure. PhD thesis, Marquette University, Milwaukee, Wisconsin

    Google Scholar 

  • Derksen J (1996) Pollen tubes: a model system for plant cell growth. Bot Acta 109: 341–345

    Google Scholar 

  • —, Rutten T, van Amstel A, de Win AHN, Doris F, Steer MW (1995a) Regulation of pollen tube growth. Acta Bot Neerl 44: 93–119

    Google Scholar 

  • — —, Lichtscheidl IK, de Win AHN, Pierson ES, Rongen G(1995b) Quantitative analysis of the distribution of organelles in tobacco pollen tubes: implications for exocytosis and endocytosis. Protoplasma 188: 267–276

    Google Scholar 

  • —, van Amstel ANM, Rutten ALM, Knuiman B, Li Y-Q, Pierson ES (1999) Pollen tubes: cellular organization and control of growth. In: Clement C, Pacini E, Audran J-C (eds) Anther and pollen. Springer, Berlin Heidelberg New York Tokyo, pp 119–133

    Google Scholar 

  • De Win AH, Knuiman B, Pierson ES, Geurts H, Kengen HMP, Derksen J (1996) Development and cellular organization ofPinus sylvestris pollen tubes. Sex Plant Reprod 9: 93–101

    Google Scholar 

  • Ferguson C, Teeri TT, Siika-Aho M, Read SM, Bacic A (1998) Location of cellulose and callose in pollen tubes and grains ofNicotiana tabacum. Planta 206: 452–460

    Google Scholar 

  • Franklin-Tong VE, Drøbak BK, Allan AC, Watkins PAC, Trewavas AJ (1996) Growth of pollen tubes ofPapaver rhoeas is regulated by a slow-moving calcium wave propagated by inositol 1,4,5-triphosphate. Plant Cell 8: 1305–1321

    PubMed  Google Scholar 

  • Geitmann A, Hudak J, Venningerholz F, Walles B (1995) Immunogold localization of pectin and callose pollen grains and pollen tubes ofBrugmansia suaveolens: implications for the self incompatibility reaction. J Plant Physiol 147: 225–235

    Google Scholar 

  • Johri BM (1992) Haustorial role of pollen tubes. Ann Bot 70: 471–475

    Google Scholar 

  • Knox JP, Linstead PJ, King J, Cooper C, Roberts K (1990) Pectin esterification is spatially regulated both within walls and between developing tissues of root apices. Planta 181: 512–521

    Google Scholar 

  • Knox RB (1984) Pollen pistil interactions. In: Linskens HF, Heslop-Harrison J (eds) Cellular interactions. Springer, Berlin Heidelberg New York Tokyo, pp 508–608 (Pirson A, Zimmermann MH [eds] Encyclopedia of plant physiology, vol 17)

    Google Scholar 

  • Kroh M, Knuiman B (1982) Ultrastructure of cell wall and plugs of tobacco pollen tubes after chemical extraction of polysaccharides. Planta 154: 241–250

    Google Scholar 

  • Lancelle SA, Hepler PK (1988) Cytochalasin-induced ultrastructural alterations inNicotiana pollen tubes. Protoplasma Suppl 2: 65–75

    Google Scholar 

  • — —, (1992) Ultrastructure of freeze-substituted pollen tubes ofLilium longiflorum. Protoplasma 167: 215–230

    Google Scholar 

  • Lazzaro MD (1996) The actin microfilament network within elongating pollen tubes of the gymnospermPicea abies (Norway spruce). Protoplasma 194: 186–194

    Google Scholar 

  • Li YQ, Chen F, Linskens HF, Cresti M (1994) Distribution of unesterified and esterified pectins in cell walls of pollen tubes. Sex Plant Reprod 7: 145–152

    Google Scholar 

  • —, Faleri C, Geitmann A, Zhang HQ, Cresti M (1995a) Immunogold localization of arabinogalactan proteins, unesterified and esterified pectins in pollen grains and pollen tubes ofNicotiana tabacum L. Protoplasma 189: 26–36

    Google Scholar 

  • —, Fang C, Faleri C, Ciampolini F, Linskens HF, Cresti M (1995b) Presumed phylogenetic basis of pectin deposition pattern in pollen tube walls and the stylar structure of angiosperms. Proc Kon Ned Akad Wetensch 98: 39–44

    Google Scholar 

  • Linskens HF, Esser K (1957) Über eine spezifische Anfärbung der Pollenschläuche und die Zahl der Kallosepropfen nach Selbstung und Fremdung. Naturwissenschaften 44: 16

    Google Scholar 

  • Martens P, Waterkeyn L (1961) Structure du pollen “ailé” chez les conifères. Cellule 62: 28–222

    Google Scholar 

  • Miki-Hirosige H, Nakamura S (1982) Process of metabolism during pollen tube wall formation. J Electron Microsc 31: 51–62

    Google Scholar 

  • Pierson ES, Cresti M (1992) Cytoskeleton and cytoplasmic organization of pollen and pollen tubes. Int Rev Cytol 140: 73–125

    Google Scholar 

  • —, Miller DD, Callaham DA, van Aken J, Shipley AM, Rivers BA, Cresti M, Hepler PK (1994) Pollen tube growth is coupled to the extracellular calcium ion flux and the extracellular calcium gradient: effect of BAPTA-type buffers and hypertonic media. Plant Cell 6: 1815–1828

    PubMed  Google Scholar 

  • —, Li YQ, Zhang HQ, Willemse MTM, Linskens HF, Cresti M (1995) Pulsatory growth of pollen tubes: investigation of a possible relationship with the periodic distribution of cell wall components. Acta Bot Neerl 44: 121–128

    Google Scholar 

  • Sassen MMA (1964) Fine structure of petunia pollen grain and pollen tube. Acta Bot Neerl 13: 175–181

    Google Scholar 

  • Singh H (1978) Embryology of gymnosperm. Borntraeger, Berlin (Handbuch der Pflanzenanatomie, vol 10, part 2)

    Google Scholar 

  • Steer MW, Steer JM (1989) Pollen tube tip growth. New Phytol 111: 323–358

    Google Scholar 

  • Stone BA, Clarke AE (1992) Chemistry and biology of (1 → 3)-β-glucans. La Trobe University Press, Bundoora, Victoria

    Google Scholar 

  • Taylor PL, Hepler PK (1997) Pollen germination and tube growth. Annu Rev Plant Physiol Plant Mol Biol 48: 461–491

    PubMed  Google Scholar 

  • Terasaka O, Niitsu T (1994) Differential roles of microtubule and actin-myosin cytoskeleton in the growth ofPinus pollen tubes. Sex Plant Reprod 7: 264–272

    Google Scholar 

  • Waterkeyn L (1957) Callose microsporocytaire et callose pollinique. In: HF Linskens (ed) Pollen physiology and fertilization. North-Holland, Amsterdam, pp 52–58

    Google Scholar 

  • Willemse MTM (1971a) Gamétogénèse male dePinus sylvestris: morphologie et évaluation approximative des organites. Ann Univ ARERS 9: 127–132

    Google Scholar 

  • Willemse MTM (1971b) Morphological and quantitative changes in the population of cell organelles during microsporogenesis ofPinus sylvestris L. Ill: morphological changes during the tetrad stage and in the young microspore. A quantitative approach to the changes in the population of cell organelles. Acta Bot Neerl 20: 498–523

    Google Scholar 

  • Wolters-Arts AMC, van Amstel ANM, Derksen J (1993) Tracing cellulose microflbril orientations in inner primary walls. Protoplasma 175: 102–111

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Jan Derksen.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Derksen, J., Li, Y.q., Knuiman, B. et al. The wall ofPinus sylvestris L. pollen tubes. Protoplasma 208, 26–36 (1999). https://doi.org/10.1007/BF01279072

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01279072

Keywords

Navigation