Summary
The cytochalasins, known as inhibitors of various processes involving motility in plant and animal cells, induce far-reaching structural changes in the cytoplasm and walls of pollen tubes without destroying the capacity for subsequent growth in normal media. The fine structure of tubes of Endymion non-scriptus modified by cytochalasin D suggests that the changes all stem directly or indirectly from the interruption of the longrange cyclosis along the tube axis, which is sustained throughout the period of normal growth. The elimination of this movement breaks down the the pattern of flow responsible for the sorting-out process that maintains the characteristic zonation of organelles and other inclusions at the apex of the extending tube, and leads gradually to re-distribution of the vacuoles and membranes in the vegetative cell, the disposition of which is normally correlated with the longitudinally oriented flow pathways. Random local migrations of organelles and other inclusions of greater amplitude than is to be expected from Brownian movement continue in the tubes in the presence of cytochalasin D, indicating that the motility system is not wholly destroyed. Following the interruption of concerted axial movement, the polysaccharide wall-precursor bodies (P-particles), normally inserted into the wall mainly in the apical part of the tube during tip growth, gradually become dispersed throughout the tube and are incorporated in the wall at random, entering even into the intine of the parent pollen grain.
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References
Cooper JA (1987) Effects of cytochalasin and phalloidin on actin. J Cell Biol 105:1472–1478
Dickinson HG, Lawson J (1975) Pollen tube growth in the stigma of Oenothera organensis following compatible and incompatible intraspecific pollinations. Proc R Soc Ser B 188:327–344
Franke W, Herth W, Van der Woude WF, Morré DJ (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
Heslop-Harrison J (1987) Pollen germination and pollen-tube growth. Int Rev Cytol 107:1–78
Heslop-Harrison J, Heslop-Harrison Y (1982) The growth of the grass pollen tube. 1. Characteristics of the polysaccharide particles (“ P-particles”) associated with apical growth. Protoplasma 112:71–80
Heslop-Harrison J, Heslop-Harrison Y (1985) Germination of stress-tolerant Eucalyptus pollen. J Cell Sci 73:135–137
Heslop-Harrison J, Heslop-Harrison Y (1989) Cytochalasin effects on structure and movement in the pollen tube of Iris. Sex Plant Reprod 2:27–37
Heslop-Harrison J, Heslop-Harrison Y (1990) Dynamic aspects of apical zonation in the angiosperm pollen tube. Sex Plant Reprod 3:187–194
Iwanami Y (1956) Protoplasmic movement in pollen grains and tubes. Phytomorphology 6:288–296
Johnson LV, Walsh ML, Bockus BJ, Chen LB (1981) Monitoring of relative mitochondrial membrane potential in living cells by fluorescent microscopy. J Cell Biol 88:526–535
Kroh M, Knuiman B (1982) Ultrastructure of cell wall and plugs of tobacco pollen tubes after chemical extraction of polysaccharides. Planta 154:241–250
Lancelle SA, Hepler PK (1988) Cytochalasin-induced structural alterations in Nicotiana pollen tubes. Protoplasma [Suppl 2] 65–75
Lin J, Uwate WJ, Stallman V (1977) Ultrastructural localisation of acid phosphatase in the pollen tubes of Prunus avium L. (sweet cherry). Planta 135:183–190
Mascarenhas JP, La Fountain J (1972) Protoplasmic streaming, cytochalasin B and the growth of the pollen tube. Tissue Cell 4:11–14
Palevitz BA (1980) Comparative effects of phalloidin and cytochalasin B on motility and morphogenesis in Allium. Can J Bot 58:773–785
Picton JM, Steer MW (1981) Determination of secretory vesicle production rates by dictyosomes in pollen tubes of Tradescantia using cytochalasin D. J Cell Sci 49:261–272
Rosen WG, Gawlick SR, Dashek WV, Siegesmund KA (1964) Fine structure and cytochemistry of Lilium pollen tubes. Am J Bot 51:61–71
Steer MW, Steer JM (1989) Pollen tube tip growth. New Phytol 111:323–358
Wessels NK, Spooner BS, Ash JF, Bradley MO, Luduena MA, Taylor EL, Wrenn JT, Yamada KM (1971) Microfilaments in cellular and developmental process. Science 171:335–343
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Heslop-Harrison, J., Heslop-Harrison, Y., Cresti, M. et al. Ultrastructural features of pollen tubes of Endymion non-scriptus modified by cytochalasin D. Sexual Plant Reprod 4, 73–80 (1991). https://doi.org/10.1007/BF00196491
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DOI: https://doi.org/10.1007/BF00196491