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. 1978 Oct 1;79(1):110–120. doi: 10.1083/jcb.79.1.110

Calcium control of ciliary arrest in mussel gill cells

PMCID: PMC2110218  PMID: 359573

Abstract

After several hours in 20 mM sodium phosphate and 40 mM KCI (pH 7.4) or similar simple solutions, ciliated cells exfoliate en masse from stripped gill epithelium of freshwater mussels, e.g., Elliptio complanatus. Three types of ciliated cells--lateral (L), laterofrontal (LF), and frontal (F)--can be distiniguished and counted separately in the suspensions. About one-half of the cells of each type remain motile. Motility is unaffected by addition of 10(-5) M A23187 or 10(-2) M Ca+2 added separately, but when ionophore and Ca+2 are added together, ciliary beat is largely arrested. Treatment of the cells with Triton X-100 (Rohm & Haas Co., Philadelphia, Pa.) results in a total loss of motility as the ciliary membrane becomes disrupted. Such models can be reactivated by addition of ATP and Mg+2. All ciliated cell types are reactivated to about the same extent. At least 80% of the activity of the untreated preparation returns. Ca+2-EGTA buffers added to the reactivating solutions permit titration of free Ca+2 concentration vs. percent motility. Activity is unchanged for all cell types at Ca+2 less than 10(-7) M; at 10(-6) Ca+2, L cilia of all cell types are arrested differentially, whereas at Ca+2 greater than 10(-4) M most cilia of all cell types are arrested. We conclude: (a) that increasing cytoplasmic Ca+2 is directly responsible for ciliary arrest, (b) that the readily reversible physiological arrest response of the L cilia in the intact gill is caused by a rise in free Ca+2 in narrow limits from ca. 5 x 10(- 7) M to ca. 8 x 10(-7) M, and (c) that the site which is sensitive to Ca+2 is part of the ciliary axoneme or the basal apparatus.

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Selected References

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

  1. Ashley C. C. An estimate of calcium concentration changes during the contraction of single muscle fibres. J Physiol. 1970 Sep;210(2):133P–134P. [PubMed] [Google Scholar]
  2. Brokaw C. J., Josslin R., Bobrow L. Calcium ion regulation of flagellar beat symmetry in reactivated sea urchin spermatozoa. Biochem Biophys Res Commun. 1974 Jun 4;58(3):795–800. doi: 10.1016/s0006-291x(74)80487-0. [DOI] [PubMed] [Google Scholar]
  3. Holwill M. E., McGregor J. L. Effects of calcium on flagellar movement in the trypanosome Crithidia oncopelti. J Exp Biol. 1976 Aug;65(1):229–242. doi: 10.1242/jeb.65.1.229. [DOI] [PubMed] [Google Scholar]
  4. Mackie G. O. Neuroid conduction and the evolution of conducting tissues. Q Rev Biol. 1970 Dec;45(4):319–332. doi: 10.1086/406645. [DOI] [PubMed] [Google Scholar]
  5. Motokawa T., Satir P. Laser-induced spreading arrest of Mytilus gill cilia. J Cell Biol. 1975 Aug;66(2):377–391. doi: 10.1083/jcb.66.2.377. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Naito Y., Kaneko H. Reactivated triton-extracted models o paramecium: modification of ciliary movement by calcium ions. Science. 1972 May 5;176(4034):523–524. doi: 10.1126/science.176.4034.523. [DOI] [PubMed] [Google Scholar]
  7. PORTZEHL H., CALDWELL P. C., RUEEGG J. C. THE DEPENDENCE OF CONTRACTION AND RELAXATION OF MUSCLE FIBRES FROM THE CRAB MAIA SQUINADO ON THE INTERNAL CONCENTRATION OF FREE CALCIUM IONS. Biochim Biophys Acta. 1964 May 25;79:581–591. doi: 10.1016/0926-6577(64)90224-4. [DOI] [PubMed] [Google Scholar]
  8. SATIR P. STUDIES ON CILIA. THE FIXATION OF THE METACHRONAL WAVE. J Cell Biol. 1963 Aug;18:345–365. doi: 10.1083/jcb.18.2.345. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Satir P., Sale W. S. Tails of Tetrahymena. J Protozool. 1977 Nov;24(4):498–501. doi: 10.1111/j.1550-7408.1977.tb00999.x. [DOI] [PubMed] [Google Scholar]

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