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. 1982 Sep 1;94(3):607–612. doi: 10.1083/jcb.94.3.607

Lidocaine reversibly inhibits fertilization in Chlamydomonas: a possible role for calcium in sexual signalling

PMCID: PMC2112220  PMID: 7130274

Abstract

A flagellar adhesion-induced signal sent during the mating reaction of the biflagellate alga, Chlamydomonas reinhardtii, initiates release of cell-wall-degrading enzymes, activation of mating structures, and cell fusion. The nature of this signal is unknown, but it may be mediated by an adhesion-induced change (activation) of flagellar tips. The studies reported here show that lidocaine, a local anesthetic that is reported to interfere with the movement of divalent cations across cell membranes, reversibly blocks cell wall loss and gametic fusion without blocking adhesion or flagellar tip activation. In these experiments lidocaine inhibited both the initial rates and the extent of wall loss and zygote formation. Studies with gametes of a paralyzed flagellar mutant, pf 17, revealed that lidocaine also blocked flagellar surface motility (visualized as movement of polystyrene beads) at concentrations of the inhibitor which also prevented gametic fusion. The concentration of lidocaine required to block cell fusion was dependent on the concentration of calcium or magnesium in the medium. In the absence of added calcium, 0.5 mM lidocaine inhibited fusion by 70%. In 0.5 mM calcium, 0.5 mM lidocaine had no effect on fusion and 2 mM lidocaine was required for 90% inhibition. The results suggest that divalent cations may play a critical role in sexual signalling in Chlamydomonas.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Bessen M., Fay R. B., Witman G. B. Calcium control of waveform in isolated flagellar axonemes of Chlamydomonas. J Cell Biol. 1980 Aug;86(2):446–455. doi: 10.1083/jcb.86.2.446. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Bloodgood R. A., Leffler E. M., Bojczuk A. T. Reversible inhibition of Chlamydomonas flagellar surface motility. J Cell Biol. 1979 Sep;82(3):664–674. doi: 10.1083/jcb.82.3.664. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bloodgood R. A. Motility occurring in association with the surface of the Chlamydomonas flagellum. J Cell Biol. 1977 Dec;75(3):983–989. doi: 10.1083/jcb.75.3.983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Collins F., Epel D. The role of calcium ions in the acrosome reaction of sea urchin sperm: regulation of exocytosis. Exp Cell Res. 1977 Apr;106(1):211–222. doi: 10.1016/0014-4827(77)90258-0. [DOI] [PubMed] [Google Scholar]
  5. Forest C. L., Goodenough D. A., Goodenough U. W. Flagellar membrane agglutination and sexual signaling in the conditional GAM-1 mutant of Chlamydomonas. J Cell Biol. 1978 Oct;79(1):74–84. doi: 10.1083/jcb.79.1.74. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Friedmann I., Colwin A. L., Colwin L. H. Fine-structural aspects of fertilization in Chlamydomonas reinhardi. J Cell Sci. 1968 Mar;3(1):115–128. doi: 10.1242/jcs.3.1.115. [DOI] [PubMed] [Google Scholar]
  7. Goodenough U. W., Adair W. S., Caligor E., Forest C. L., Hoffman J. L., Mesland D. A., Spath S. Membrane-membrane and membrane-ligand interactions in Chlamydomonas mating. Soc Gen Physiol Ser. 1980;34:131–152. [PubMed] [Google Scholar]
  8. Hoffman J. L., Goodenough U. W. Experimental dissection of flagellar surface motility in Chlamydomonas. J Cell Biol. 1980 Aug;86(2):656–665. doi: 10.1083/jcb.86.2.656. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Hyams J. S., Borisy G. G. Isolated flagellar apparatus of Chlamydomonas: characterization of forward swimming and alteration of waveform and reversal of motion by calcium ions in vitro. J Cell Sci. 1978 Oct;33:235–253. doi: 10.1242/jcs.33.1.235. [DOI] [PubMed] [Google Scholar]
  10. Kung C., Chang S. Y., Satow Y., Houten J. V., Hansma H. Genetic dissection of behavior in paramecium. Science. 1975 May 30;188(4191):898–904. [PubMed] [Google Scholar]
  11. LEWIN R. A. Mutants of Chlamydomonas moewusii with impaired motility. J Gen Microbiol. 1954 Dec;11(3):358–363. doi: 10.1099/00221287-11-3-358. [DOI] [PubMed] [Google Scholar]
  12. Mesland D. A., Hoffman J. L., Caligor E., Goodenough U. W. Flagellar tip activation stimulated by membrane adhesions in Chlamydomonas gametes. J Cell Biol. 1980 Mar;84(3):599–617. doi: 10.1083/jcb.84.3.599. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. SAGER R., GRANICK S. Nutritional control of sexuality in Chlamydomonas reinhardi. J Gen Physiol. 1954 Jul 20;37(6):729–742. doi: 10.1085/jgp.37.6.729. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Schmidt J. A., Eckert R. Calcium couples flagellar reversal to photostimulation in Chlamydomonas reinhardtii. Nature. 1976 Aug 19;262(5570):713–715. doi: 10.1038/262713a0. [DOI] [PubMed] [Google Scholar]
  15. Seeman P. The membrane actions of anesthetics and tranquilizers. Pharmacol Rev. 1972 Dec;24(4):583–655. [PubMed] [Google Scholar]
  16. Shapiro B. M., Schackmann R. W., Gabel C. A. Molecular approaches to the study of fertilization. Annu Rev Biochem. 1981;50:815–843. doi: 10.1146/annurev.bi.50.070181.004123. [DOI] [PubMed] [Google Scholar]
  17. Snell W. J., Dentler W. L., Haimo L. T., Binder L. I., Rosenbaum J. L. Assembly of chick brain tubulin onto isolated basal bodies of Chlamydomonas reinhardi. Science. 1974 Jul 26;185(4148):357–360. doi: 10.1126/science.185.4148.357. [DOI] [PubMed] [Google Scholar]
  18. Snell W. J. Mating in Chlamydomonas: a system for the study of specific cell adhesion. I. Ultrastructural and electrophoretic analyses of flagellar surface components involved in adhesion. J Cell Biol. 1976 Jan;68(1):48–69. doi: 10.1083/jcb.68.1.48. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Snell W. J., Moore W. S. Aggregation-dependent turnover of flagellar adhesion molecules in Chlamydomonas gametes. J Cell Biol. 1980 Jan;84(1):203–210. doi: 10.1083/jcb.84.1.203. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Snell W. J., Roseman S. Kinetics of adhesion and de-adhesion of Chlamydomonas gametes. J Biol Chem. 1979 Nov 10;254(21):10820–10829. [PubMed] [Google Scholar]
  21. Snell W. J. Study of the release of cell wall degrading enzymes during adhesion of Chlamydomonas gametes. Exp Cell Res. 1982 Mar;138(1):109–119. doi: 10.1016/0014-4827(82)90096-9. [DOI] [PubMed] [Google Scholar]
  22. Snell W. K. Flagellar adhesion and deadhesion in Chlamydomonas gametes: effects of tunicamycin and observations on flagellar tip morphology. J Supramol Struct Cell Biochem. 1981;16(4):371–376. doi: 10.1002/jsscb.1981.380160407. [DOI] [PubMed] [Google Scholar]
  23. Watanabe T., Flavin M. Nucleotide-metabolizing enzymes in Chlamydomonas flagella. J Biol Chem. 1976 Jan 10;251(1):182–192. [PubMed] [Google Scholar]

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