Stretch-activated calcium channels relay fast calcium waves propagated by calcium-induced calcium influx

Biology of the Cell

Volumn 99, Issue 3, 2007, Pages 175-184

  Jaffe, Lionel F ^a  

^a MARINE BIOLOGICAL LABORATORY   (United States)

Author keywords

Calcium wave; Calcium induced calcium influx; Flagella; Metachronal wave; Stretch activated calcium channel

Indexed keywords

CALCIUM CHANNEL; CALCIUM ION; DYNEIN ADENOSINE TRIPHOSPHATASE; KINESIN; MYOSIN ADENOSINE TRIPHOSPHATASE; TUBULIN;

ARTHROPOD; ARTICLE; BIOLOGICAL MODEL; BRYOZOA; CALCIUM TRANSPORT; CELL MEMBRANE; CONTROLLED STUDY; EQUISETUM; EUKARYOTIC FLAGELLUM; FISH; FROG; HUMAN; INSECT; MAMMAL CELL; MECHANICAL STIMULATION; MECHANOTRANSDUCTION; MICROTUBULE; MOLLUSC; NONHUMAN; PREDICTION; PRIORITY JOURNAL; PROTOZOON; SEA URCHIN; WORM;

ANIMALS; CALCIUM; CALCIUM CHANNELS; CALCIUM SIGNALING; CELL MEMBRANE; CELL MOVEMENT; CELL POLARITY; MICROFILAMENTS; MICROTUBULES; MODELS, BIOLOGICAL; STRESS, MECHANICAL;

ANURA; ARTHROPODA; BRANCHIOSTOMA LANCEOLATUM; BRYOZOA; ECHINOIDEA; EQUISETUM; HEXAPODA; MAMMALIA; MOLLUSCA; POLYCHAETA; PROTOZOA; TRACHEOPHYTA;

EID: 33847745390     PISSN: 02484900     EISSN: None     Source Type: Journal    
DOI: 10.1042/BC20060031     Document Type: Article

References (91)

1. Baccetti, B., Burrini, A.G., Dallai, R., Pallini, V., Pereiti, P., Piantelli, F., Rosati, F. and Selmi, G. (1973a) Structure and function in the spermatozoan of Bacillus rossius. The spermatozoon of arthropoda. XIX. J. Ultrastruct. Res. Suppl. 12, 5-73
2. Baccetti, B., Burrini, G., Dallai, R., Giusti, F., Mazzini, M., Renieri, T., Rosati, F. and Selmi, G. (1973b) Structure and function in the spermatozoan of Tenebrio molitor (the spermatozoon of Arthropoda. XX). J. Mechanochem. Cell Motil. 2, 149-161
3. Baccetti, B., Gibbons, B.H. and Gibbons, I.R. (1989) Bidirectional swimming in spermatozoa of Tephritid flies. J. Submicrosc. Cytol. Pathol. 21, 619-625
4. Bilderback, D.E., Bilderback, D.E., Jahn, T.L. and Fonseca, J.R. (1973) The release mechanism and locomotor behavior of Equisetum sperm. Am. J. Bot. 60, 796-801
5. Bannai, H., Yoshimura, M., Takahashi, K. and Shingyoji, C. (2000) Calcium regulation of microtubule sliding in reactivation sea urchin sperm flagella. J. Cell Sci. 113, 831-839
6. Bressac, C., Joly, D., Devaus, J., Serres, C., Feneux, B. and Lachaise, D. (1991) Comparative kinetics of short and long sperm in sperm dimorphic Drosophila species. Cell Motil. Cytoskeleton 19, 269-274
7. Brokaw, C.J. (1963) Movement of the flagella of Polytoma uvella. J. Exp. Biol. 40, 149-156
8. Brokaw, C.J. (1972) Flagellar movement: a sliding filament model. Science 178, 455-462
9. Brokaw, C.J. and Wright, L. (1963) Bending waves of the posterior flagellum of Ceratium. Science 142, 116-170
10. Brust-Mascher, I. and Webb, W.W. (1998) Calcium waves induced by large voltage pulses in fish keratocytes. Biophys. J. 75, 1669-1678
11. Charles, A.C., Kodali, S.K. and Tyndale, R.F. (1996) Intercellular calcium waves in neurons. Mol. Cell Neurosci. 7, 337-353
12. 2+]i waves in cardiac myocytes. Am. J. Physiol. 270, C148-C159
13. Chevrier, C. and Dacheux, J.-L. (1992) Evolution of the flagellar waveform of ram spermatozoa in relation to the degree of epididymal maturation. Cell Motil. Cytoskeleton 23, 8-18
14. Chiesa, A., Rapizzi, E., Tosello, V., Pinton, P., de Virgilio, M., Fogarty, K.E. and Rizzuto, R. (2001) Recombinant aequorin and green flluorescent protein as valuable tools in the study of cell signalling. Biochem. J. 355, 1-12
15. Clary-Meinesz, C.F., Cosson, J., Huitorel, P. and Blaive, B. (1992) Temperature effect on the ciliary beat frequency of human nasal and trachael ciliated cells. Biol. Cell 76, 335-338
16. Cleveland, L.R. and Cleveland, B.T. (1966) The locomotory waves of Koruga, Deltotrichonympha and Mixotricha. Arch. Protistenkd. 109, 39-63
17. Corey, D.P., Garcia-Anoveros, J., Holt, J.R., Kwan, K.Y, Lin, S.Y., Vollrath, M.A., Amalfitano, A., Cheung, E.L., Derfler, B.H., Duggan, A., Geleoc, G.S., Gray, P.A., Hoffman, M.P., Rehm, H.L., Tamasauskas, D. and Zhang, D.S. (2004) TRPA1 is a candidate for the mechanosensitive transduction channel of vertebrate hair cells. Nature 432, 723-729
18. Cosson, J. (1992) The covalent oscillator: a paradigm accounting for the sliding/bend mechanism and wave propagation in cilia and flagella. Biol. Cell 76, 319-327
19. Créton, R. and Jaffe, L.F. (2001) Chemiluminescence microscopy as a tool in biomedical research. Biotechniques 31, 1098-1105
20. Dumollard, R., Carroll, J., Dupont, G. and Sardet, C. (2002) Calcium wave pacemakers in eggs. J. Cell Sci. 115, 3557-3564
21. Ehlers, K.M., Samuel, A.D.T., Berg, H.C. and Montgomery, R. (1996) Do cyanobacteria swim using surface waves? Proc. Natl. Acad. Sci. U.S.A. 93, 8340-8343
22. Eshel D. and Priel, Z. (1987) Characterization of metachronal wave of beating cilia on frog's palate epithelium in tissue culture. J. Physiol. 388, 1-8
23. Featherstone, N.C., Jesudason, E.C., Connell, M.G., Fernig, D.G., Wray, S., Losty, P.D. and Burdyga, T.V. (2005) Spontaneous propagating calcium waves underpin airway peristalsis in embryonic rat lung. Am. J. Respir. Cell Mol. Biol. 33, 153-160
24. Feller, M.B., Butts, D.A., Aaron, H.L., Rokhsar, D.S. and Shatz, D.J. (1997) Dynamic processes shape spatiotemporal properties of retinal waves. Neuron 19, 293-306
25. Gheber, L. and Priel, Z. (1987) Extraction of cilium beat parameters by the combined application of photoelectric measurements and computer simulation. Biophys. J. 72, 449-462
26. Gibbons, I.R. (1980) Intermittent swimming in live sea urchin sperm. J. Cell Biol. 84, 1-12
27. Gibbons, I.R. (1982) Sliding and bending in sea urchin sperm flagella. Symp. Soc. Exp. Biol. 35, 225-287
28. Gilkey, J.C., Jaffe, L.F., Ridgway, E.B. and Reynolds, G.T. (1978) A free calcium wave traverses the activating egg of the medaka, Oryzias latipes. J. Cell Biol. 76, 448-466
29. Gray, J. and Hancock (1955) The propulsion of sea-urchin spermatozoa. J. Exp. Biol. 32, 802-814
30. Guthrie, P.B., Knappenberger, J., Segal, M., Bennett, M.V.L., Charles, A.C. and Kater, S.B. (1999) ATP released from astrocytes mediates glial calcium waves. J. Neurosci. 19, 520-528
31. 2+ and not cAMP. Dev. Biol. 250, 208-217
32. Holland, E.M., Hartmann, H., Uhl, R. and Hegemann, P. (1997) Control of phobic behavioral responses by rhodopsin-induced photocurrents in Chlamydomonas. Biophys. J. 73, 1395-1401
33. Holwill, M.E.J. (1965) The motion of Strigomonas oncopelti. J. Exp. Biol. 42, 125-137
34. Holwill, M.E.J. and Silvester, N.R. (1965) The thermal dependence of flagellar activity in Strigomonas oncopelti. J. Exp. Biol. 42, 537-544
35. Holwill, M.E.J. and McGregor, J.L. (1976) Effects of calcium on flagellar movement in the trypanosome Crithidia oncopelti. J. Exp. Biol. 65, 229-242
36. Howard, D.R., Trantow, C.M. and Thaler, C.D. (2004) Motility of a biflagellate sperm: waveform analysis and cyclic nucleotide activatrion. Cell Motil. Cytoskeleton 59, 120-130
37. Hu, H. and Sachs, F. (1997) Stretch-activated ion channels in the heart. J. Mol. Cardiol. 29, 1511-1523
38. Huang, J.-B., Kindzelskii, S.L., Clark, A.F. and Petty, H. (2004) Identification of calcium channels promoting calcium waves in HT1080 tumor cells. Cancer Res. 64, 2482-2489
39. Hyams, J.S. and Borisy, G.G. (1978) Isolated flagellar apparatus of Chlamydomonas: characterization of forward swimming and alteration of waveform and reversal of motion by calciuim ions in vitro. J. Cell Sci. 33, 235-253
40. Ishide, N., Urayama, T., Inoue, K.-I., Komaru, T. and Takashima, T. (1990) Propagation and collision characteristics of calcium waves in rat myocytes Am. J. Physiol. 259, H940-H950
41. Ishijima, S., Ishijima, S.A. and Afzelius, B.A. (1994) Movement of Myzostomium spermatozoa: calcium ion regulation of swimming direction. Cell Motil. Cytoskeleton 28, 145-142
42. Ishijima, S., Ishijima, S.A. and Afzelius, B.A. (1999) Movement of Turritella spermatozoa: direction of propagation and chirality of flagellar bends. Cell Motil. Cytoskeleton 44, 85-95
43. Ishijima, S., Baba, S.A., Mohri, H. and Suarez, S.S. (2002) Quantitative analysis of flagellar movement in hyperactivated and acrosome-reacted golden hamster spermatozoa. Mol. Reprod. Dev. 61, 376-384
44. 2+ and completed by cAMP. Mol. Reprod. Dev. 73, 1129-1139
45. 2+ waves sneaking under the plasma membrane in endothelial cells. Circ. Res. 95, e11-e21
46. Jaffe, L.F. (1999) Organization of early development by calcium patterns. BioEssays 21, 657-667
47. Jaffe, L.F. (2003) The propagation speeds of calcium action potentials are remarkably invariant. Biol. Cell 95, 343-355
48. Jaffe, L.F. and Créton, R. (1998) On the conservation of calcium wave speeds. Cell Calcium 24, 1-8
49. Jeulin, C., Lewin, L.M., Chevrier, C. and Schoevaert-Brossault, D. (1996) Changes in flagellar movement of rat spermatozoa along the length of the epididymis: manual and computor-aided image analysis. Cell Motil. Cytoskeleton 35, 147-161
50. 2+ waves in Langendorff-perfused rat heart revealed by real-time confocal microscopy. Circ. Res. 86, 1093-1099
51. Kindzelskii, A.L. and Petty, H.R. (2003) Intracellular calcium waves accompany neutrophil polarization, formylmethylleucyl-phenylalanine stimulation and phagocytosis: a high speed microscopy study. J. Immunol. 170, 64-72
52. 2+ and cAMP. Cell Motil. Cytoskeleton 8, 324-332
53. Linhart, O., Cosson, J., Mims, S.D., Selton, W.L. and Rodina, M. (2002) Effects of ions on the motility of fresh and demembranated paddle fish (Polyodon spathula) spermatozoa. Reproduction 124, 713-719
54. 2+ release in cultured neonatal cardiac myocytes. Circ. Res. 74, 979-990
55. Lowndes, A.G. (1941) On flagellar movement in unicellular organisms. Proc. Zool. Soc. London 111, 111-134
56. Lowndes, A.G. (1944) On the swimming of uniflagellate organisms. Proc. Zool. Soc. London 113A, 99-197
57. Lowndes, A.G. (1945) Swimming of Monas stigmata. Nature 155, 579
58. Lucas, A.M. (1931) An investigation of the nervous system as a possible factor in the regulation of ciliary activity of the lamellibranch gill. J. Morphol. Physiol. 51, 147-185
59. Machemer, H. (1972) Temperature influences on ciliary beat and metachronal coordination in Paramecium. J. Mechanochem. Cell Motil. 1, 57-66
60. Machemer, H. (1974) In Ciliary activity and metachronism in protozoa. In Cilia and Flagella (Sleigh, M.A., ed.), pp. 199-286, Academic Press, London
61. Martinac, B. (2004) Mechanosensitive ion channels: molecules of mechanotransductin. J. Cell Sci. 117, 2449-2460
62. Mortimer, S.T., Schoevaert, D., Swan, M.A. and Mortimer, D. (1997) Quantitative observations of flagellar motility of capacitating human spermatozoa. Hum. Reprod. 12, 1006-1012
63. Naitoh, Y. and Kaneko, H. (1972) Reactivated Triton-extracted models of Paramecium: modification of ciliary movement by calcium ions. Science 176, 523-524
64. Okajima, A. (1953) Studies on the metachronal wave in Opalina I. Electrical stimulation with the microelectrode. Jpn. J. Zool. 10, 87-100
65. Pasey, A.A., Cosson, J.C. and Bentley, M.G. (1994) Intermittent swimming in the spermatozoa of the lugworm Arenicola marina (L.) (annelida: polychaeta). Cell Motil. Cytoskeleton 29, 186-194
66. Pitta, T.P., Sherwood, E.E., Kobel, A.M. and Berg, H.C. (1997) Calcium is required for swimming by the nonflagellated cyanobacterium Synechoccus strain WH8113. J. Bacteriol. 179, 2524-2528
67. Reber, B.F.X. and Schindelholz, B. (1996) Detection of a trigger zone of bradykinin-induced fast calcium waves in PC12 neurites. Pflügers Arch. 432, 893-903
68. Rikmenspoel, R. (1978) The equation of motion for sperm flagella. Biophys. J. 23, 177-205
69. Riisgard, H.U., Nielsen, K.K., Fuchs, J., Rasmussen, B.F., Obst, M. and Funch, P. (2004) Ciliary feeding structures and particle capture mechanism in the freshwater bryozoan Plumatella repens (Phylactolaemata). Invertebr. Biol. 123, 156-167
70. Rintoul, G.L. and Bainbridge, K.G. (2003) Effects of calcium buffers and calbindin D-28k upon histamineinduced calcium oscillations and calcium waves in HeLa cells. Cell Calcium 34, 131-144
71. 2+ dynamics with genetically encoded bioluminescent reporters. Eur. J. Neurosci. 21, 597-610
72. Sala-Newby, G.B., Badminton, M.N., Evans, W.H., George, C.H., Jones, H.E., Kendall, J.M., Ribiero, A.R. and Campbell, A.K. (2000) Targeted bioluminescence indicators in living cells. Methods Enzymol. 305, 479-498
73. Samuel, A.D.T., Petersen, J.D. and Reese, T.S. (2001) Envelope structure of Synechoccus sp. WH8113, a nonflagellated swimming cyanobacterium. BMC Microbiol. 1, 4
74. Satir, P. (1968) Studies on cilia III. Further studies on the cilium tip and a 'sliding filament' model of ciliary motility. J. Cell Biol. 39, 77-94
75. Schmidt, J.A. and Eckert, R. (1976) Calcium couples flagellar reversal to photostimulation in Chlamydomonas Reinhardttii. Nature 262, 713-715
76. Schoevaert, D., Krishnashwamy, S., Couturier, M. and Marano, F. (1988) Ciliary beat and cell motility of Dunaliella: computer analysis of high speed microcinematography. Biol. Cell 62, 229-240
77. Serres, C., Feneux, D. and Berthon, B. (1991) Decrease of internal free calcium and human sperm movement. Cell Motil. Cytoskeleton 18, 228-240
78. Sleigh, M.A. (1956) Metachronism and frequency of beat in the peristomal cilia of Stentor. J. Exp. Biol. 33, 15-28
79. Sleigh, M.A. (1960) The form of beat in cilia of Stentor and Opalina. J. Exp. Biol. 37, 1-10
80. Sleigh, M.A. (1974) Metachronism of cilia of metazoa. In Cilia and Flagella (Sleigh, M.A., ed.), pp. 287-304, Academic Press, London
81. Spungin, B. and Silberberg, A. (1984) Stimulation of mucus secretion, ciliary activity, and transport in frog palate epithelium. Am. J. Physiol. 247, C299-C308
82. Stokes, M.D. and Holland, N.D. (1995) Ciliary hovering in larval lancelets (Amphioxus). Biol. Bull. 188, 231-233
83. Sugrue, P., Hirons, M.R., Adam, J.U. and Holwill, M.E.J. (1988) Flagellar wave reversal in the kinetoplastid flagellate Crithidia oncopelti. Biol. Cell 63, 127-131
84. Takamatsu, T., Minamikawa, T., Kawachi, H. and Fujita, S. (1991) Imaging of calcium wave propagation in guinea pig ventricular cell pairs by confocal laser scanning microscopy. Cell Struct. Funct. 16, 341-346
85. Tamm, S.L. (1999) Locomotory waves of Koruga and Deltotrichonympha: flagella wag the cell. Cell Motil. Cytoskeleton 43, 145-158
86. Trafford, A.W., Lipp, P., O'Neill, Niggli, E. and Eisner, D.A. (1995) Propagating calcium waves initiated by local caffeine application in rat ventricular myocytes. J. Physiol. 489, 319-326
87. 2+ dependent waveform conversion in the flagellar axoneme of Chlamydomonas mutants lacking the central-pair/radial spoke system. Cell Motil. Cytoskeleton 38, 22-28
88. Werner, M., Tscheulin, T., Speck, T., Zissler, D. and Peschke, K. (2002) Ultrastructure and motility pattern of the spermatozoa of Aleochara curtula (coleoptera, staphylinidae). Arthropod Struct. Dev. 31, 243-254
89. Wooley, D.M. (1998) Studies on the eel sperm flagellum. 2. The kinematics of normal motility. Cell Motil. Cytoskeleton 39, 233-245
90. Wussling, M. and Mair, T. (1999) Calcium waves in rat cardiac myocytes underlie the principles of selforganization in excitable media. Lect. Notes Phys. 532, 151-163
91. Wussling, M.H.P. and Salz, H. (1996) Nonlinear propagation of spherical calcium waves in rat cardiac myocytes. Biophys. J. 70, 1144-1153