Revisiting the role of H+ in chemotactic signaling of sperm

Journal of General Physiology

Volumn 124, Issue 2, 2004, Pages 115-124

  Solzin, Johannes ^a,b,d   Helbig, Annika ^a,b   Van, Qui ^a,b   Brown, Joel E ^b,c   Hildebrand, Eilo ^a   Weyand, Ingo ^a,b   Kaupp, Benjamin ^a,b  

^a FORSCHUNGSZENTRUM JÜLICH   (Germany)

^b MARINE BIOLOGICAL LABORATORY   (United States)

^c ALBERT EINSTEIN COLLEGE OF MEDICINE   (United States)

^d UNIVERSITY OF COLOGNE   (Germany)

Author keywords

Ca2+; Chemotaxis; Cyclic nucleotides; Fertilization; Kinetics

Indexed keywords

CALCIUM ION; CYCLIC AMP; CYCLIC GMP; CYCLIC NUCLEOTIDE; GUANOSINE TRIPHOSPHATE; GUANYLATE CYCLASE; IMIDAZOLE DERIVATIVE; PROTON; SODIUM ION; SODIUM PROTON EXCHANGE PROTEIN; SPERM ACTIVATING PEPTIDE; UNCLASSIFIED DRUG;

ANIMAL CELL; ARTICLE; CALCIUM CELL LEVEL; CHEMOTAXIS; ENZYME ACTIVATION; FERTILIZATION; ION EXCHANGE; KINETICS; MALE; MEMBRANE PERMEABILITY; NONHUMAN; PEPTIDE ANALYSIS; PH; RECEPTOR BINDING; RESACT; SEA URCHIN; SIGNAL TRANSDUCTION; SPERM;

ANIMALS; ARBACIA; CALCIUM SIGNALING; CHEMOTAXIS; HYDROGEN-ION CONCENTRATION; MALE; PROTONS; SEA URCHINS; SPERMATOZOA; STRONGYLOCENTROTUS PURPURATUS;

EID: 3843113236     PISSN: 00221295     EISSN: None     Source Type: Journal    
DOI: 10.1085/jgp.200409030     Document Type: Article

References (43)

1. + channels by the egg peptide speract. Proc. Natl. Acad. Sci. USA. 89:6001-6005.
2. Christen, R., R.W. Schackmann, and B.M. Shapiro. 1982. Elevation of the intracellular pH activates respiration and motility of sperm of the sea urchin, Strongylocentrotus purpuratus. J. Biol. Chem. 257: 14881-14890.
3. Christen, R., R.W. Schackmann, and B.M. Shapiro. 1983. Metabolism of sea urchin sperm. Interrelationships between intracellular pH, ATPase activity, and mitochondrial respiration. J. Biol. Chem. 258:5392-5399.
4. i increase induced by speract. J. Biol. Chem. 268:22408-22413.
5. + channel activated by speract. J. Biol. Chem. 268: 22402-22407.
6. 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.
7. Dangott, L.J., and D.L. Garbers. 1984. Identification and partial characterization of the receptor for speract. J. Biol. Chem. 259: 13712-13716.
8. Dangott, L.J., J.E. Jordan, R.A. Bellet, and D.L. Garbers. 1989. Cloning of the mRNA for the protein that crosslinks to the egg peptide speract. Proc. Natl. Acad. Sci. USA. 86:2128-2132.
9. Darszon, A., P. Labarca, T. Nishigaki, and F. Espinosa. 1999. Ion channels in sperm physiology. Physiol. Rev. 79:481-510.
10. Darszon, A., C. Beltrán, R. Felix, T. Nishigaki, and C.L. Treviño, 2001. Ion transport in sperm signaling. Dev. Biol. 240:1-14.
11. Garbers, D.L. 1989. Molecular basis of fertilization. Annu. Rev. Biochem. 58:719-742.
12. Garbers, D.L., H.D. Watkins, J.R. Hansbrough, A. Smith, and K.S. Misono. 1982. The amino acid sequence and chemical synthesis of speract and of speract analogues. J. Biol. Chem. 257:2734-2737.
13. Gauss, R., R. Seifert, and U.B. Kaupp. 1998. Molecular identification of a hyperpolarization-activated channel in sea urchin sperm. Nature. 393:583-587.
14. Goldstein, S.F. 1979. Starting transients in sea urchin sperm flagella. J. Cell Biol. 80:61-68.
15. Gray, J. 1928. The effect of dilution on the activity of sea urchin spermatozoa. Br. J. Exp. Biol. 5:337-344.
16. 2+ channels during the egg jelly-induced acrosome reaction of sea urchin sperm. J. Biol. Chem. 264:19593-19599.
17. Hansbrough, J.R., and D.L. Garbers. 1981a. Sodium-dependent activation of sea urchin spermatozoa by speract and monensin. J. Biol. Chem. 256:2235-2241.
18. Hansbrough, J.R., and D.L. Garbers. 1981b. Speract - purification and characterization of a peptide associated with eggs that activates spermatozoa. J. Biol. Chem. 256:1447-1452.
19. Harumi, T., K. Hoshino, and N. Suzuki. 1992. Effects of sperm-activating peptide 1 on Hemicentrotus pulcherrimus spermatozoa in high potassium sea water. Dev. Growth Differ. 34:163-172.
20. Johnson, C.H., D.L. Clapper, M.M. Winkler, H.C. Lee, and D. Epel. 1983. A volatile inhibitor immobilizes sea urchin sperm in semen by depressing the intracellular pH. Dev. Biol. 98:493-501.
21. Kaupp, U.B., J. Solzin, J.E. Brown, A. Helbig, V. Hagen, M. Beyermann, E. Hildebrand, and I. Weyand. 2003. The signal flow controling chemotaxis of sea urchin sperm. Nat. Cell Biol. 5:109-117.
22. + exchange system in flagella isolated from sea urchin spermatozoa. J. Biol. Chem. 259:15315-15319.
23. Lee, H.C. 1984b. Sodium and proton transport in flagella isolated from sea urchin spermatozoa. J. Biol. Chem. 259:4957-4963.
24. + exchange in sea urchin spermatozoa flagellar membrane vesicles studied with an entrapped pH probe. J. Biol. Chem. 260:10794-10799.
25. + exchange in sea urchin spermatozoa through membrane potential changes induced by the egg peptide speract. J. Biol. Chem. 261:16026-16032.
26. Lee, H.C., C. Johnson, and D. Epel. 1983. Changes in internal pH associated with initiation of motility and acrosome reaction of sea urchin sperm. Dev. Biol. 95:31-45.
27. Matsumoto, M., J. Solzin, A. Helbig, V. Hagen, S.-I. Ueno, O. Kawase, Y. Maruyama, M. Ogiso, M. Godde, H. Minakata, et al. 2003. A sperm-activating peptide controls a cGMP-signaling pathway in starfish sperm. Dev. Biol. 260:314-324.
28. Miller, R.L. 1985. Sperm chemo-orientation in the metazoa. In Biology of Fertilization, Vol. 2: Biology of the Sperm. C.B. Metz and A. Monroy, editors. Academic Press, New York. 275-337.
29. Nishigaki, T., F.Z. Zamudio, L.D. Possani, and A. Darszon. 2001. Time-resolved sperm responses to an egg peptide measured by stopped-flow fluorometry. Biochem. Biophys. Res. Commun. 284: 531-535.
30. Ogawa, K., H. Takai, A. Ogiwara, E. Yokota, T. Shimizu, K. Inaba, and H. Mohri. 1996. Is outer arm dynein intermediate chain 1 multifunctional? Mol. Biol. Cell. 7:1895-1907.
31. Ohtake, H. 1976. Respiratory behaviour of sea-urchin spermatozoa. I. Effect of pH and egg water on the respiratory rate. J. Exp. Zool. 198:303-311.
32. Repaske, D.R., and D.L. Garbers. 1983. A hydrogen ion flux mediates stimulation of respiratory activity by speract in sea urchin spermatozoa. J. Biol. Chem. 258:6025-6029.
33. Reynaud, E., L. De la Torre, O. Zapata, A. Liévano, and A. Darszon. 1993. Ionic bases of the membrane potential and intracellular pH changes induced by speract in swollen sea urchin sperm. FEBS Lett. 329:210-214.
34. 2+] in sea urchin sperm by the egg peptide speract. J. Biol. Chem. 261:8719-8728.
35. Schackmann, R.W., R. Christen, and B.M. Shapiro. 1981. Membrane potential depolarization and increased intracellular pH accompany the acrosome reaction of sea urchin sperm. Proc. Natl. Acad. Sci. USA. 78:6066-6070.
36. i, phosphorylcreatine shuttles, and sperm motility. Bioessays. 3:100-103.
37. Suzuki, N., H. Shimomura, E.W. Radany, C.S. Ramarao, G.E. Ward, J.K. Bentley, and D.L. Garbers. 1984. A peptide associated with eggs causes a mobility shift in a major plasma membrane protein of spermatozoa. J. Biol. Chem. 259:14874-14879.
38. Tombes, R.M., and B.M. Shapiro. 1985. Metabolite channeling: a phosphorylcreatine shuttle to mediate high energy phosphate transport between sperm mitochondrion and tail. Cell. 41:325-334.
39. 2+ in sea urchin spermatozoa. Proc. Natl. Acad. Sci. USA. 83:9055-9059.
40. van Dorsten, F.A., M. Wyss, T. Wallimann, and K. Nicolay. 1997. Activation of sea-urchin sperm motility is accompanied by an increase in the creatine kinase exchange flux. Biochem. J. 325:411-416.
41. Ward, C.R., and G.S. Kopf. 1993. Molecular events mediating sperm activation. Dev. Biol. 158:9-34.
42. 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.
43. Wood, C.D., A. Darszon, and M. Whitaker. 2003. Speract induces calcium oscillations in the sperm tail. J. Cell Biol. 161:89-101.