Real-time analysis of the role of Ca 2 in flagellar movement and motility in single sea urchin sperm

Journal of Cell Biology

Volumn 169, Issue 5, 2005, Pages 725-731

  Wood, Christopher D ^a   Nisihigaki, Takuya ^a   Furuta, Toshiaki ^b   Baba, Shoji A ^c   Darszon, Alberto ^a  

^a INSTITUTO DE BIOTECNOLOGÍA   (Mexico)

^b TOHO UNIVERSITY   (Japan)

^c OCHANOMIZU UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM;

ANIMAL CELL; ARTICLE; BIOLOGICAL MODEL; CALCIUM CELL LEVEL; CALCIUM TRANSPORT; CELL COMPARTMENTALIZATION; CELL INFILTRATION; FLAGELLUM; FLUORESCENCE; MALE; NONHUMAN; PRIORITY JOURNAL; REGULATORY MECHANISM; SEA URCHIN; SPERM; SPERMATOZOON MOTILITY; STROBOSCOPY;

ANIMALS; CALCIUM; CALCIUM CHANNEL BLOCKERS; CALCIUM CHANNELS; CALCIUM SIGNALING; CELL MOVEMENT; CHEMOTAXIS; CYCLIC GMP; FERTILIZATION; FLAGELLA; MALE; SIGNAL TRANSDUCTION; SPERMATOZOA; STRONGYLOCENTROTUS PURPURATUS; TIME FACTORS;

ECHINOIDEA; MAMMALIA;

EID: 22344450118     PISSN: 00219525     EISSN: None     Source Type: Journal    
DOI: 10.1083/jcb.200411001     Document Type: Article

References (30)

1. Akaike, N., P.G. Kostyuk, and Y.V. Osipchuk. 1989. Dihydropyridine- sensitive low-threshold calcium channels in isolated rat hypothalamic neurones. J. Physiol. 412:181-195.
2. Baba, S.A., and Y. Mogami. 1985. An approach to digital image analysis of bending shapes of eukaryotic flagella and cilia. Cell Motil. Cytoskeleton.5:475-489.
3. Brokaw, C.J. 1974. Calcium and flagellar response during the chemotaxis of bracken spermatozoids. J. Cell. Physiol. 83:151-158.
4. Brokaw, C.J. 1979. Calcium-induced asymmetrical beating of triton-demembranated sea urchin sperm flagella. J. Cell Biol. 82:401-411.
5. Chung, M.K., and H. Kim. 2002. Volume-activated chloride currents from human fibroblasts: blockade by nimodipine. Gen. Physiol. Biophys. 21:85-101.
6. 2+ permeability by cAMP is coordinated through the pHi increase induced by speract. J. Biol. Chem. 268:22408-22413.
7. Cook, S.P., C.J. Brokaw, C.H. Muller, and D.F. Babcock. 1994. Sperm chemotaxis: egg peptides control cytosolic calcium to regulate flagellar responses. Dev. Biol. 165:10-19.
8. Cosson, J., P. Huitorel, and C. Gagnon. 2003. How spermatozoa come to be confined to surfaces. Cell Motil. Cytoskeleton. 54:56-63.
9. Cosson, M.P., D. Carre, and J. Cosson. 1984. Sperm chemotaxis in siphonophores. II. Calcium-dependent asymmetrical movement of spermatozoa induced by the attractant. J. Cell Sci. 68:163-181.
10. 2+ fluctuations in sperm physiology. Int. Rev. Cytol. 243:79-172.
11. Doering, C.J., and G.W. Zamponi. 2003. Molecular pharmacology of high voltage-activated calcium channels. J. Bioenerg. Biomembr. 35:491-505.
12. Eisenbach, M. 1999. Sperm chemotaxis. Rev. Reprod. 4:56-66.
13. Escobar, A.L., P. Velez, A.M. Kim, F. Cifuentes, M. Fill, and J.L. Vergara. 1997. Kinetic properties of DM-nitrophen and calcium indicators: rapid transient response to flash photolysis. Pflugers Arch. 434:615-631.
14. Furuta, T., H. Takeuchi, M. Isozaki, Y. Takahashi, M. Kanehara, M. Sugimoto, T. Watanabe, K. Noguchi, T.M. Dore, T. Kurahashi, et al. 2004. Bhc-cNMPs as either water-soluble or membrane-permeant photoreleasable cyclic nucleotides for both one- and two-photon excitation. ChemBio-Chem. 5:1119-1128.
15. + channels as targets for specific immunomodulation. Trends Pharmacol. Sci. 25:280-289.
16. 2+ is required for the acrosome reaction in sea urchin sperm. Dev. Biol. 236:220-229.
17. Goodwin, L.O., N.B. Leeds, I. Hurley, G.W. Cooper, R.G. Pergolizzi, and S. Benoff. 1998. Alternative splicing of exons in the α1 subunit of the rat testis L-type voltage-dependent calcium channel generates germ linespecific dihydropyridine binding sites. Mol. Hum. Reprod. 4:215-226.
18. Harumi, T., K. Hoshino, and N. Suzuki. 1992. Effects of sperm-activating peptide I on Hemicentrotus pulcherrimus spermatozoa in high potassium sea water. Dev. Growth Differ. 34:163-172.
19. Ishikawa, M., H. Tsutsui, J. Cosson, Y. Oka, and M. Morisawa. 2004. Strategies for sperm chemotaxis in the siphonophores and ascidians: a numerical simulation study. Biol. Bull. 206:95-102.
20. Kaupp, U.B., J. Solzin, E. Hildebrand, J.E. Brown, A. Helbig, V. Hagen, M. Beyermann, F. Pampaloni, and I. Weyand. 2003. The signal flow and motor response controling chemotaxis of sea urchin sperm. Nat. Cell Biol. 5:109-117.
21. Kazazoglou, T., R.W. Schackmann, M. Fosset, and B.M. Shapiro. 1985. Calcium channel antagonists inhibit the acrosome reaction and bind to plasma membranes of sea urchin sperm. Proc. Natl. Acad. Sci. USA.82:1460-1464.
22. Miller, R. 1985. Sperm chemo-orientation in the metazoa. In Biology of Fertilization. C. Metz and A. Monroy, editors. Academic Press Inc., New York.275-337.
23. Miller, R.L., and C.J. Brokaw. 1970. Chemotactic turning behaviour of Tubularia spermatozoa. J. Exp. Biol. 52:699-706.
24. 2+ before its increase. Dev. Biol. 272:376-388.
25. Shimomura, H., and D.L. Garbers. 1986. Differential effects of resact analogues on sperm respiration rates and cyclic nucleotide concentrations. Biochemistry. 25:3405-3410.
26. Spehr, M., G. Gisselmann, A. Poplawski, J.A. Riffell, C.H. Wetzel, R.K. Zimmer, and H. Hatt. 2003. Identification of a testicular odorant receptor mediating human sperm chemotaxis. Science. 299:2054-2058.
27. Suzuki, N., and D.L. Garbers. 1984. Stimulation of sperm respiration rates by speract and resact at alkaline extracellular pH. Biol. Reprod. 30:1167-1174.
28. Ward, G.E., C.J. Brokaw, D.L. Garbers, and V.D. Vacquier. 1985. Chemotaxis of Arbacia punctulata spermatozoa to resact, a peptide from the egg jelly layer. J. Cell Biol. 101:2324-2329.
29. Wood, C.D., A. Darszon, and M. Whitaker. 2003. Speract induces calcium oscillations in the sperm tail. J. Cell Biol. 161:89-101.
30. Yunker, A.M. 2003. Modulation and pharmacology of low voltage-activated ("T-Type") calcium channels. J. Bioenerg. Biomembr. 35:577-598.