Regulation of protein phosphorylation during sperm capacitation

Biology of Reproduction

Volumn 59, Issue 1, 1998, Pages 1-6

  Visconti, Pablo E ^a   Kopf, Gregory S ^a  

^a HOSPITAL OF THE UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BICARBONATE; CALCIUM ION; CHOLESTEROL; CYCLIC AMP; CYCLIC AMP DEPENDENT PROTEIN KINASE; FREE RADICAL; GLUCOSE; HEPARIN; SERUM ALBUMIN; TYROSINE;

ACROSOME REACTION; CELL MEMBRANE; CELL MEMBRANE POTENTIAL; CELL PH; FERTILIZATION; HUMAN; NONHUMAN; PRIORITY JOURNAL; PROTEIN PHOSPHORYLATION; SECOND MESSENGER; SHORT SURVEY; SPERMATOZOON CAPACITATION; SPERMATOZOON MOTILITY;

ANIMALS; HUMANS; MALE; PHOSPHOPROTEINS; PHOSPHORYLATION; SECOND MESSENGER SYSTEMS; SPERM CAPACITATION;

EID: 0031778295     PISSN: 00063363     EISSN: None     Source Type: Journal    
DOI: 10.1095/biolreprod59.1.1     Document Type: Short Survey

References (81)

1. Chang MC. Fertilizing capacity of spermatozoa deposited into the fallopian tubes. Nature 1951; 168:697-698.
2. Chang MC. Development of fertilizing capacity of rabbit spermatozoa in the uterus. Nature 1955; 175:1036-1037.
3. Austin CR. Observations on the penetration of the sperm into the mammalian egg. Aust J Sci Res 1951; 4:581-596.
4. Austin CR. The "capacitation" of the mammalian sperm. Nature 1952; 170:326.
5. Yanagimachi R. Mammalian fertilization. In: Knobil E, Neill JD (eds.), The Physiology of Reproduction. New York. Raven Press, Ltd.; 1994: 189-317.
6. Suarez SS. Hyperactivated motility in sperm. J Androl 1996; 17:331-335.
7. Neill J, Olds-Clarke P. A computer-assisted assay for mouse sperm hyperactivation demonstrates that bicarbonate but not bovine serum albumin is required. Gamete Res 1987; 18:121-140.
8. Florman HM, Babcock DF. Progress towards understanding the molecular basis of capacitation. CRC Uniscience-Chemistry of Fertilization 1991; 105-132.
9. Cohen-Dayag A, Eisenbach M. Potential assays for sperm capacitation in mammals. Am J Physiol Cell Physiol 1994; 267:C1167-C1176.
10. de Lamirande E, Leclerc P, Gagnon C. Capacitation as a regulatory event that primes spermatozoa for the acrosome reaction and fertilization. Mol Hum Reprod 1997; 3:175-194.
11. Cross NL. Role of cholesterol in sperm capacitation. Biol Reprod 1998; 59:7-11.
12. Florman HM, Lemos JR, Arnoult C, Kazam I, Li C, O'Toole CM. A tale of two channels: a perspective on the control of mammalian fertilization by egg-activated ion channels in sperm. Biol Reprod 1998; 59:12-16.
13. Hunter AG, Nornes HO. Characterization and isolation of a sperm-coating antigen from rabbit seminal plasma with capacity to block fertilization. J Reprod Fertil 1969; 20:419-427.
14. Carr DW, Acott TS. Inhibition of bovine spermatozoa by caudal epididymal fluid: I. Studies of a sperm motility quiescence factor. Biol Reprod 1984; 30:913-925.
15. Acott TS, Carr DW. Inhibition of bovine spermatozoa by caudal epididymal fluid: II. Interaction of pH and a quiescence factor. Biol Reprod 1984; 30:926-935.
16. Langlais J, Roberts KD. A molecular membrane model of sperm capacitation and the acrosome reaction of mammalian spermatozoa. Gamete Res 1985; 12:183-224.
17. Davis BK. Timing of fertilization in mammals: sperm cholesterol/ phospholipid ratio as a determinant of the capacitation interval. Proc Natl Acad Sci USA 1981; 78:7560-7564.
18. Davis BK, Byrne R, Hangund B. Studies on the mechanism of capacitation II. Evidence for lipid transfer between plasma membrane of rat sperm and serum albumin during capacitation in vitro. Biochim Biophys Acta 1979; 558:257-266.
19. Go KJ, Wolf DP. Albumin-mediated changes in sperm sterol content during capacitation. Biol Reprod 1985; 32:145-153.
20. Wolf DE, Hagopian SS, Isogima S. Changes in sperm plasma membrane lipid diffusibility after hyperactivation during in vitro capacitation in the mouse. J Cell Biol 1986; 102:1372-1377.
21. Wolf DE, Cardullo RA. Physiological properties of the mammalian sperm plasma membrane. In: Baccetti B (ed.), Comparative Spermatology 20 Years After. New York: Raven Press; 1991: 599-604.
22. Therien I, Manjunath P. Phospholipid-binding proteins of bovine seminal vesicles modulate HDL-and heparin-induced capacitation of spermatozoa. Biol Reprod 1996; 54(suppl 1): 62 (abstract 23).
23. Cross NL. Human seminal plasma prevents sperm from becoming acrosomally responsive to the agonist, progesterone: cholesterol is the major inhibitor. Biol Reprod 1996; 54:138-145.
24. Zarintash RJ, Cross NL. Unesterified cholesterol content of human sperm regulates the response of the acrosome to the agonist, progesterone. Biol Reprod 1996; 55:19-24.
25. Cross NL, Razy-Faulkner P. Control of human sperm intracellular pH by cholesterol and its relationship to the response of the acrosome to progesterone. Biol Reprod 1997; 56:1169-1174.
26. Visconti PE, Bailey JL, Moore GD, Pan D, Olds-Clarke P, Kopf GS. Capacitation of mouse spermatozoa. I. Correlation between the capacitation state and protein tyrosine phosphorylation. Development 1995; 121:1129-1137.
27. 2+-related changes in the capacitation state of human spermatozoa assessed by a chlortetracycline fluorescence assay. J Reprod Fertil 1993; 99:135-143.
28. Baldi E, Casana R, Falsetti C. Intracellular calcium accumulation and responsiveness to progesterone in capacitating human spermatozoa. J Androl 1991; 12:323-330.
29. Lee MA, Storey BT. Bicarbonate is essential for fertilization of mouse eggs; mouse sperm require it to undergo the acrosome reaction. Biol Reprod 1986; 34:349-356.
30. 2 is not required for zona pellucida-or progesterone-induced acrosomal exocytosis of mouse spermatozoa but is essential for capacitation. Biol Reprod 1995; 52:540-546.
31. Boatman DE, Robbins RS. Bicarbonate: carbon-dioxide regulation of sperm capacitation, hyperactivated motility, and acrosome reactions. Biol Reprod 1991; 44:806-813.
32. Visconti PE, Muschietti JP, Flawia MM, Tezon JG. Bicarbonate dependence of cAMP accumulation induced by phorbol esters in hamster spermatozoa. Biochim Biophys Acta 1990; 1054:231-236.
33. Spira B, Breitbart H. The role of anion channels in the mechanism of acrosome reaction in bull spermatozoa. Biochim Biophys Acta 1992; 1109:65-73.
34. Parkkila S, Rajaniemi H, Kellokumpu S. Polarized expression of a band 3-related protein in mammalian sperm cells. Biol Reprod 1993; 49:326-331.
35. Okamura N, Tajima Y, Sugita Y. Decrease in bicarbonate transport activities during epididymal maturation of porcine sperm. Biochem Biophys Res Commun 1988; 157:1280-1287.
36. Uguz C, Vredenburgh WL, Parrish JJ. Heparin-induced capacitation but not intracellular alkalinization of bovine sperm is inhibited by Rp-adenosine-3′,5′-cyclic monophosphothioate. Biol Reprod 1994; 51: 1031-1039.
37. 3- dependent and arylaminobenzoate-dependent regulatory mechanisms and characterization of their role in sperm capacitation. Dev Biol 1996; 173:510-520.
38. Okamura N, Tajima Y, Soejima A, Masuda H, Sugita Y. Sodium bicarbonate in seminal plasma stimulates the motility of mammalian spermatozoa through the direct activation of adenylate cyclase. J Biol Chem 1985; 260:9699-9705.
39. Garty N, Salomon Y. Stimulation of partially purified adenylate cyclase from bull sperm by bicarbonate. FEBS Lett 1987; 218:148-152.
40. Brooks DE. Epididymal function and their hormonal regulation. Aust J Biol Sci 1983; 36:205-221.
41. Eddy EM, O'Brien DA. The spermatozoon. In: Knobil E, Neill JD (eds.), The Physiology of Reproduction. New York: Raven Press; 1994: 29-77.
42. Visconti PE, Moore GD, Bailey JL, Leclerc P, Connors SA, Pan D, Olds-Clarke P, Kopf GS. Capacitation of mouse spermatozoa. II. Protein tyrosine phosphorylation and capacitation are regulated by a cAMP-dependent pathway. Development 1995; 121:1139-1150.
43. Leclerc P, de Lamirande E, Gagnon C. Cyclic adenosine 3′,5′ monophosphate-dependent regulation of protein tyrosine phosphorylation in relation to human sperm capacitation and motility. Biol Reprod 1996; 55:684-692.
44. White DR, Aitken RJ. Relationship between calcium, cyclic AMP, ATP, and intracellular pH and the capacity of hamster spermatozoa to express hyperactivated motility. Gamete Res 1989; 22:163-177.
45. Visconti PE, Johnson L, Oyaski M, Fornés M, Moss SB, Gerton GL, Kopf GS. Regulation, localization, and anchoring of protein kinase A subunits during mouse sperm capacitation. Dev Biol 1997; 192:351-363.
46. Hyne RV, Garbers DL. Regulation of guinea pig sperm adenylate cyclase by calcium. Biol Reprod 1979; 21:1135-1142.
47. Gross MK, Toscano DG, Toscano WA. Calmodulin-mediated adenylate cyclase from mammalian sperm. J Biol Chem 1987; 262:8672-8676.
48. Kopf GS, Vacquier VD. Characterization of a calmodulin stimulated adenylate cyclase from abalone spermatozoa. J Biol Chem 1984; 259: 7590-7596.
49. Okamura N, Tajima Y, Onoe S, Sugita Y. Purification of bicarbonate-sensitive sperm adenylyl cyclase by 4-acetamido-4′-isothiocyanostilbene-2,2′-disulfonic acid-affinity chromatography. J Biol Chem 1991; 266:17754-17759.
50. Galantino-Homer H, Visconti PE, Kopf GS. Regulation of protein tyrosine phosphorylation during bovine sperm capacitation by a cyclic adenosine 3′,5′-monophosphate-dependent pathway. Biol Reprod 1997; 56:707-719.
51. Carrera A, Moos J, Ning XP, Gerton GL, Tesarik J, Kopf GS, Moss SB. Regulation of protein tyrosine phosphorylation in human sperm by a calcium/calmodulin-dependent mechanism: identification of A kinase anchor proteins as major substrates for tyrosine phosphorylation. Dev Biol 1996; 180:284-296.
52. Aitken RJ, Paterson M, Fisher H, Buckingham DW, Van Duin M. Redox regulation of tyrosine phosphorylation in human spermatozoa and its role in the control of human sperm function. J Cell Sci 1995; 108:2017-2025.
53. Hunter T. Tyrosine phosphorylation: past, present and future. Biochem Soc Trans 1996; 24:307-327.
54. Clark EA, Shattil SJ, Brugge JS. Regulation of protein tyrosine kinases in platelets. TIBS 1994; 19:464-469.
55. Visconti PE, Ning XP, Fornes MW, Alvarez J, Kopf GS. Role of protein phosphorylation in sperm capacitation. Biol Reprod 1997; 56(suppl 1):35 (abstract M-27).
56. Van Haastert PJM, Van Driel R, Jastorff B, Baraniak J, Stec WJ, De Wit RJW. Competitive cAMP antagonists for cAMP-receptor proteins. J Biol Chem 1984; 259:10020-10024.
57. Takagi K, Ogawa K, Tanaka H, Satake T, Watanabe Y, Chijiwa T, Hidaka H. Relaxant effects of various xanthine derivatives: relationship to cyclic nucleotide phosphodiesterase inhibition. Adv Second Messenger Phosphoprotein Res 1992; 25:353-362.
58. Parker Botelho LH, Rothermel JD, Coombs RV, Jastorff B. cAMP analog antagonists of cAMP action. Methods Enzymol 1988; 159: 159-172.
59. Wu J, Dent P, Jelinek T, Wolfman A, Weber MJ, Sturgill TW. Inhibition of the EGF-activated MAP kinase signaling pathway by adenosine 3′,5′-monophosphate. Science 1993; 262:1065-1069.
60. Cook SJ, McCormick F. Inhibition by cAMP of ras-dependent activation of raf. Science 1993; 262:1069-1072.
61. Begum N, Graham AL, Sussman KE, Draznin B. Role of cAMP in mediating effects of fasting on dephosphorylation of insulin receptor. Am J Physiol 1992; 262:E142-E149.
62. Brautigan DL, Pinault FM. Activation of membrane protein-tyrosine phosphatase involving cAMP-and Ca/phospholipid-dependent protein kinases. Proc Natl Acad Sci USA 1991; 88:6696-6700.
63. Vredenburgh-Wilberg WL, Parrish JJ. Intracellular pH of bovine sperm increases during capacitation. Mol Reprod Dev 1995; 40:490-502.
64. Zeng Y, Clark EN, Florman HM. Sperm membrane potential: hyperpolarization during capacitation regulates zona pellucida-dependent acrosomal secretion. Dev Biol 1995; 171:554-563.
65. Arnoult C, Zeng Y, Florman HM. ZP3-dependent activation of sperm cation channels regulates acrosomal secretion during mammalian fertilization. J Cell Biol 1996; 134:637-645.
66. Alvarez JG, Storey BS. Spontaneous lipid peroxidation in rabbit epididymal spermatozoa: its effect on sperm motility. Biol Reprod 1982; 27:1102-1108.
67. Alvarez JG, Storey BS. Taurine, hypotaurine, epinephrine, and albumin inhibit lipid peroxidation in rabbit spermatozoa. Biol Reprod 1983; 29:548-555.
68. Alvarez JG, Storey BS. Assessment of cell damage caused by lipid peroxidation in rabbit spermatozoa. Biol Reprod 1984; 30:323-331.
69. Storey BS. Biochemistry of the induction and prevention of lipoperoxidative damage in human spermatozoa. Mol Hum Reprod 1997; 3: 203-213.
70. de Lamirande E, Gagnon C. Impact of reactive oxygen species on spermatozoa: a balancing act between beneficial and detrimental effects. Hum Reprod 1995; 10(suppl 1):15-21.
71. de Lamirande E, Gagnon C. Human sperm hyperactivation and capacitation as parts of an oxidative process. Free Radical Biol Med 1993; 14:157-166.
72. de Lamirande E, Gagnon C. A positive role for the superoxide anion in triggering hyperactivation and capacitation of human spermatozoa. Int J Androl 1993; 16:21-25.
73. Leclerc P, de Lamirande E, Gagnon C. Regulation of protein-tyrosine phosphorylation and human sperm capacitation by reactive oxygen derivatives. Free Radical Biol Med 1997; 22:643-656.
74. Parrish JJ, Susko-Parrish J, Winer MA, First NL. Capacitation of bovine sperm by heparin. Biol Reprod 1988; 38:1171-1180.
75. Miller DJ, Ax RL. Carbohydrates and fertilization in animals. Mol Reprod Dev 1990; 26:184-198.
76. Miller DJ, Winer MA, Ax RL. Heparin-binding proteins from seminal plasma bind to bovine spermatozoa and modulate capacitation by heparin. Biol Reprod 1990; 42:899-915.
77. Thérien I, Bleau G, Manjunath P. Phosphatidylcholine-binding proteins of bovine seminal plasma modulate capacitation of spermatozoa by heparin. Biol Reprod 1995; 52:1372-1379.
78. Parrish JJ, Susko-Parrish JL, Uguz C, First NL. Differences in the role of cyclic adenosine 3′,5′-monophosphate during capacitation of bovine sperm by heparin or oviduct fluid. Biol Reprod 1994; 51:1099-1108.
79. Mahadevan MM, Miller MM, Moutos DM. Absence of glucose decreases human fertilization and sperm movement characteristics in vitro. Hum Reprod 1997; 12:119-123.
80. Rogers BJ, Perreault SD. Importance of glycolysable substrates for in vitro capacitation of human spermatozoa. Biol Reprod 1990; 43:1064-1069.
81. Fraser LR, Herod JE. Expression of capacitation-dependent changes in chlortetracycline fluorescence patterns in mouse spermatozoa requires a suitable glycolysable substrate. J Reprod Fertil 1990; 88:611-621.