Skip to main content
Log in

Dependence of ciliary reversal inParamecium on extracellular Ca2+ concentration

  • Published:
Journal of comparative physiology Aims and scope Submit manuscript

Summary

The locomotor behaviour ofParamecium caudatum was studied in solutions of various low Ca2+ concentration, adjusted by EGTA, in the presence of K+, Na+and other substances, which under normal conditions induce ciliary reversal.

A distinct [Ca2+]0 of ca. 6·10−8mol/l was found below which ciliary reversal failed to occur. Monovalent cations shifted this threshold towards higher [Ca2+]0 values. Previous incubation at different [K+ 0 and [Ca2+]0 did not influence the threshold concentration. At low [Ca2+]0 monovalent cations caused the surface membrane to disrupt, and the organisms swam backward until they became immobile. The threshold [Ca2+]0 for this phenomenon induced by 67 mmol/l NaCl was 2·10−7 mol/l. The critical Ca2+ activity required for reversal was slightly lower for live paramecia than for those whose membrane was disintegrated. The intraciliary Ca2+ concentration, [Ca2+]i; at rest was estimated to be less than 5·10−8 mol/l.

The results support the assumption that the increment in [Ca2+]i underlying ciliary reversal is caused by passive Ca2+ influx through voltagesensitive Ca channels in the ciliary membrane. The effect of monovalent cations on the critical [Ca2+] is explained mainly by their depolarizing action which lowers the effective voltage for Ca2+ entry.

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

References

  • Akita YK (1941) Electrolytes inParamecium. Mem Fac Sci Agr Taihoku Imp Univ 23:99–120

    Google Scholar 

  • Baker PF, Hodgkin AL, Ridgway EB (1971) Depolarization and calcium entry in squid giant axons. J Physiol (Lond) 218:709–755

    Google Scholar 

  • Browning JL, Nelson DL (1976) Biochemical studies of the excitable membrane ofParamecium aurelia. I.45Ca2+ fluxes across resting and excited membrane. Biochim Biophys Acta 448:338–351

    Google Scholar 

  • Caldwell PC (1970) Calcium chelation and buffers. In: Cuthbert AW (ed) Symp on Calcium and Cellular Function. MacMillan, London, pp 10–16

    Google Scholar 

  • Chang S-Y, Kung C (1976) Selection and analysis of a mutantParamecium tetraurelia lacking behavioral response to tetraethylammonium. Genet Res Camb 27:97–107

    Google Scholar 

  • DiPolo R, Requena J, Brinley FJ Jr., Mullins LJ, Scarpa A, Tiffert T (1976) Ionized calcium concentrations in squid axons. J Gen Physiol 67:433–467

    Google Scholar 

  • Dryl S (1958) Photographic registration of movement of Protozoa. Bull Acad Pol Sci Ser Sci Biol 6:429–430

    Google Scholar 

  • Dryl S (1959) Effects of adaptation to environment on chemotaxis ofParamecium caudatum. Acta Biol Exp (Warsaw) 19:83–93

    Google Scholar 

  • Dunlap K (1977) Localization of calcium channels inParamecium caudatum. J Physiol (Lond) 271:119–133

    Google Scholar 

  • Eckert R (1972) Bioelectric control of ciliary activity. Science 176:473–481

    Google Scholar 

  • Eckert R, Naitoh Y, Machemer H (1976) Calcium in the bioelectric and motor functions ofParamecium. In: Duncan CJ (ed) Calcium in biological systems. Cambridge Univ Press, London, pp 233–255

    Google Scholar 

  • Ferguson ML (1957) Photographic technique for quantitative studies of paramecia and other motile cells. Physiol Zool 30:208–215

    Google Scholar 

  • Grebecki A (1965) Role of Ca2+ ions in the excitability of protozoan cell. Decalcification, recalcification, and the ciliary reversal inParamecium caudatum. Acta Protozool 3:275–289

    Google Scholar 

  • Hildebrand E (1975) Significance of the competition between calcium and other cations for the conductivity control in sensory membranes. Verh Dtsch Zool Ges 1974:24–28

    Google Scholar 

  • Hook C, Hildebrand E (1980) Excitability ofParamecium and the significance of negative surface charges. J Math Biol 9:347–360

    Google Scholar 

  • Jennings HS (1899) Studies on reactions to stimuli in unicellular organisms. II. The mechanism of the motor reactions ofParamecium. Am J Physiol 2:311–341

    Google Scholar 

  • Kamada T, Kinosita H (1940) Calcium-potassium factor in ciliary reversal ofParamecium. Proc Imp Acad (Tokyo) 16:125–130

    Google Scholar 

  • Kung C (1971) Genetic mutants with altered systems of excitation inParamecium aurelia. II. Mutagenesis, screening and genetic analysis of the mutants. Genetics 69:29–45

    Google Scholar 

  • Machemer H (1974) Frequency and directional responses of cilia to membrane potential changes inParamecium. J Comp Physiol 92:293–316

    Google Scholar 

  • Machemer H, Eckert R (1975) Ciliary frequency and orientational responses to clamped voltage steps inParamecium. J Comp Physiol 104:247–260

    Google Scholar 

  • Machemer H, Peyer J de (1977) Swimming sensory cells: Electrical membrane parameters, receptor properties and motor control in ciliated Protozoa. Verh Dtsch Zool Ges 1977:86–110

    Google Scholar 

  • Martinac B, Hildebrand E (1981) Electrically induced Ca2+ transport across the membrane ofParamecium caudatum measured by means of flow-through technique. Biochim Biophys Acta 649:244–252

    Google Scholar 

  • Meech RW, Standen NB (1975) Potassium activation inHelixaspersa neurons under voltage clamp: A component mediated by Ca influx. J Physiol (Lond) 249:211–239

    Google Scholar 

  • Naitoh Y (1968) Ionic control of the reversal response of cilia inParamecium caudatum. A calcium hypothesis. J Gen Physiol 51:85–103

    Google Scholar 

  • Naitoh Y (1969) Control of the orientation of cilia by adenosine-triphosphate, calcium, and zinc in glycerol-extractedParamecium caudatum. J Gen Physiol 53:517–529

    Google Scholar 

  • Naitoh Y, Eckert R (1968) Electrical properties ofParamecium caudatum: Modification by bound and free cations. Z Vergl Physiol 61:427–452

    Google Scholar 

  • Naitoh Y, Kaneko H (1972) Reactivated Triton-extracted models ofParamecium: Modification of ciliary movement by calcium ions. Science 176:523–524

    Google Scholar 

  • Naitoh Y, Kaneko H (1973) Control of ciliary activities by adenosinetriphosphate and divalent cations in Triton-extracted models ofParamecium caudatum. J Exp Biol 58:657–676

    Google Scholar 

  • Ogawa Y (1968) The apparent binding constant of glycol-etherdiaminetetraacetic acid for calcium at neutral pH. J Biochem (Tokyo) 64:255–257

    Google Scholar 

  • Ogura A, Takahashi K (1976) Artificial deciliation causes loss of calcium-dependent response inParamecium. Nature 264:170–172

    Google Scholar 

  • Oliphant JF (1942) Reversal of ciliary action inParamecium induced by chemicals. Physiol Zool 15:443–452

    Google Scholar 

  • Párducz B (1959) Reizphysiologische Untersuchungen an Ziliaten. VIII. Ablauf der Fluchtreaktion bei allseitiger und anhaltender Reizung. Ann Hist-Nat Mus Natl Hung 51:227–246

    Google Scholar 

  • Schein SJ (1976) Nonbehavioral selection for pawns, mutants ofParamecium aurelia with decreased excitability. Genetics 84:453–468

    Google Scholar 

  • Sillén LG, Martell AE (eds) (1964) Stability constants of metalion complexes. Special Publication No. 17. The Chemical Society, London

    Google Scholar 

  • Yamaguchi T (1963) Time changes in Na, K and Ca contents ofParamecium caudatum afer γ-irradation. Annot Zool Jpn 36:55–65

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Hildebrand, E., Dryl, S. Dependence of ciliary reversal inParamecium on extracellular Ca2+ concentration. J. Comp. Physiol. 152, 385–394 (1983). https://doi.org/10.1007/BF00606243

Download citation

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00606243

Keywords

Navigation