Abstract
The intention of this investigation was to acquire more concise information about the nature of the action potential of Dionaea muscipula Ellis and the different types of cells generating and conducting it. It is shown by microelectrode measurements that, besides the sensory cells, all the major tissues of the trap lobes are excitable, firing action potentials with pronounced after-hyperpolarizations. The action potentials are strictly dependent on Ca2+. Their peak depolarizations are shifted 25–27 mV in a positive direction after a tenfold increase in external Ca2+ concentration. Perfusions with 1 mM ethylene glycol-bis(β-aminoethyl ether)-N,N,N′,N′-tetraacetic acid (EGTA) or 1 mM LaCl3 completely inhibit excitability. Magnesium ions only slightly affect the peak depolarizations but considerably prolong action potentials. Sodium azide and 2,4-dinitrophenol also abolish excitation, probably by reducing the intracellular ATP concentration. Furthermore, it is tested whether the sensory cells can be distinguished from the other cells of the trap by their electrical behaviour. The resting potentials of sensory cells (-161±7 mV) and mesophyll cells (-155±8 mV) are of the same magnitude. Changes in external ion concentrations affect resting and action potentials in both cell types in a similar way. Additional freeze-fracture studies of both cell types reveal similar numbers and distributions of intramembrane particles on the fracture faces of the plasma membrane, which is most likely the mechanosensor. These findings stress the view that the high mechanosensitivity of the sensory hair results from its anatomy and not from a specialized perception mechanism. It is proposed that trap closure is triggered by a rise in the cytoplasmic concentration of Ca2+ or a Ca2+-activated regulatory complex, which must exceed a threshold concentration. Since the Ca2+ influx during a single action potential does not suffice to reach this threshold, at least two stimulations of the trap are necessary to elicit movement.
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Abbreviations
- DNP:
-
2,4-dinitrophenol
- EF:
-
exoplasmic fracture face
- EGTA:
-
ethylene glycol-bis(β-aminoethyl ether)-N,N,N′,N′-tetraacetic acid
- Em :
-
membrane potential
- Em,r :
-
resting potential
- PF:
-
protoplasmic fracture face
References
Ashida, J. (1934) Studies on the leaf movement of Aldrovanda vesiculosa. Mem. Coll. Sci. Kyoto Imp. Univ. Ser. B 9, 141–244
Benolken, R.M., Jacobson, S.L. (1970) Response properties of a sensory hair excised from Venus's flytrap. J. Gen. Physiol. 56, 64–82
Branton, D., Bullivant, S., Gilula, N.B., Karnovsky, M.J., Moor, H., Mühlethaler, K., Northcote, D.H., Packer, L., Satir, B., Satir, P., Speth, V., Staehelin, L.A., Steere, R.L., Weinstein, R.S. (1975) Freeze fracture nomenclature. Science 190, 54–56
Brown, W.H. (1916) The mechanism of movement and the duration of the effect of stimulation in the leaves of Dionaea. Am. J. Bot. 3, 68–90
Brown, W.H., Sharp, L.W. (1910) The closing response in Dionaea. Bot. Gaz. 49, 290–302
Buchen, B., Hensel, D., Sievers, A. (1983) Polarity in mechanoreceptor cells of Dionaea muscipula Ellis. Planta 158, 458–468
Burdon-Sanderson, J. (1873) Note on the electrical phenomena which accompany stimulation of the leaf of Dionaea muscipula. Proc. Royal Soc. 21, 495–496
Dargel, R. (1981) Mitochondrieller Elektronentransport. pp. 75, 124–129; VEB Gustav Fischer Verlag, Jena
Eaton, D.C., Brodwick, M.S. (1980) Effects of barium on the potassium conductance of squid axon. J. Gen. Physiol. 75, 727–750
Gaffey, C.T., Mullins, L.J. (1958) Ion fluxes during the action potential in Chara. J. Physiol. 144, 505–524
Haberlandt, G. (1906) Sinnesorgane im Pflanzenreich zur Perzeption mechanischer Reize, 2. Auflage, pp. 133–143, Engelmann, Leipzig
Hayama, T., Shimmen, T., Tazawa, M. (1979) Participation of Ca2+ in cessation of cytoplasmic streaming induced by membrane excitation in Characeae internodal cells. Protoplasma 99, 305–321
Hodick, D., Sievers, A. (1986) The influence of Ca2+ on the action potential in mesophyll cells of Dionaea muscipula Ellis. Protoplasma 133, 83–84
Hope, A.B. (1961) Ionic relations of cells of Chara australis: The action potential. Aust. J. Biol. Sci. 14, 312–322
Iijima, T., Sibaoka, T. (1985) Membrane potentials in excitable cells of Aldrovanda vesiculosa trap-lobes. Plant Cell Physiol. 26, 1–13
Jacobson, S.L. (1974) The effect of ionic environment on the response of the sensory hair of Venus's flytrap. Can. J. Bot. 52, 1293–1302
Keifer, D.W., Lucas, W.J. (1982) Potassium channels in Chara corallina. Plant Physiol. 69, 781–788
Keifer, D.W., Spanswick, R.M. (1979) Correlation of adenosine triphosphate levels in Chara corallina with the activity of the electrogenic pump. Plant Physiol. 64, 165–168
Kessler, R.J., Tyson, C.A., Green, D.E. (1976) Mechanism of uncoupling in mitochondria: uncouplers as ionophores for cycling cations and protons. Proc. Natl. Acad. Sci. USA 73, 3141–3145
Kojima, H., Katou, K., Okamoto, H. (1985) Homeostatic regulation of membrane potential by an electrogenic ion pump against change in the K+ concentration of the extra- and intra-organ perfusion solution. Plant Cell Physiol. 26, 351–359
Lichtner, F.T., Spanswick, R.M. (1977) Ion relations in Dionaea. (Abstr.) Plant Physiol. 59, Suppl., 84
Richards, J.L., Hope, A.B. (1974) The role of protons in determining membrane electrical characteristics in Chara corallina. J. Membr. Biol. 16, 121–144
Shiina, T., Tazawa, M. (1987) Demonstration and characterization of Ca2+ channel in tonoplast-free cells of Nitellopsis obtusa. J. Membr. Biol. 96, 263–276
Shimmen, T., Tazawa, M. (1977) Control of membrane potential and excitability of Chara cells with ATP and Mg2+. J. Membr. Biol. 37, 167–192
Sibaoka, T. (1962) Excitable cells in Mimosa. Science 137, 226
Sibaoka, T. (1966) Action potentials in plant organs. Symp. Soc. Exp. Biol. 20, 49–74
Von Guttenberg, H. (1959) Die physiologische Anatomie seismonastisch reaktionsfähiger Organe. In: Handbuch der Pflanzenphysiologie Bd. 17/1, pp. 175–191, Ruhland, W., Hrsg. Springer, Berlin Heidelberg New York
Williams, M., Mozingo, H. (1971) The fine structure of the trigger hair in Venus's Flytrap. Am. J. Bot. 58, 532–539
Williamson, R.E., Ashley, C.C. (1982) Free Ca2+ and cytoplasmic streaming in the alga Chara. Nature 296, 647–651
Zimmermann, U., Beckers, F. (1978) Generation of action potentials in Chara corallina by turgor pressure changes. Planta 138, 173–179
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Dedicated to Professor Karl-Ernst Wohlfarth-Bottermann on the occasion of his 65th birthday
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Hodick, D., Sievers, A. The action potential of Dionaea muscipula Ellis. Planta 174, 8–18 (1988). https://doi.org/10.1007/BF00394867
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DOI: https://doi.org/10.1007/BF00394867