Theriogenology
Volume 74, Issue 3 , Pages 413-423 , August 2010

Ice-age endurance: the effects of cryopreservation on proteins of sperm of common carp, Cyprinus carpio L

  • P. Li

      Affiliations

    • University of South Bohemia in Ceske Budejovice, Faculty of Fisheries and Protection of Waters, Research Institute of Fish Culture and Hydrobiology, Zatisi 728/II, 389 25 Vodnany, Czech Republic
    • Key Laboratory of Freshwater Biodiversity Conservation and Utilization, Ministry of Agriculture, Yangtze River Fisheries Research Institute, Chinese Academy of Fishery Science, Jingzhou, Hubei, China
    • Corresponding Author InformationCorresponding author: Tel.: (420) 387 774 611; fax: (420) 387 774 634
  • ,
  • M. Hulak

      Affiliations

    • University of South Bohemia in Ceske Budejovice, Faculty of Fisheries and Protection of Waters, Research Institute of Fish Culture and Hydrobiology, Zatisi 728/II, 389 25 Vodnany, Czech Republic
  • ,
  • P. Koubek

      Affiliations

    • Institute of Biotechnology, AS CR, v.v.i., Videnska 1083, 142 20 Prague 4, Czech Republic
  • ,
  • M. Sulc

      Affiliations

    • Institute of Microbiology, AS CR, v.v.i., Videnska 1083, 142 20 Prague 4, Czech Republic
  • ,
  • B. Dzyuba

      Affiliations

    • University of South Bohemia in Ceske Budejovice, Faculty of Fisheries and Protection of Waters, Research Institute of Fish Culture and Hydrobiology, Zatisi 728/II, 389 25 Vodnany, Czech Republic
    • Institute for Problems of Cryobiology and Cryomedicine of the National Academy of Sciences of Ukraine, Pereyaslavskaya str., 23, 61015 Kharkov, Ukraine
  • ,
  • S. Boryshpolets

      Affiliations

    • University of South Bohemia in Ceske Budejovice, Faculty of Fisheries and Protection of Waters, Research Institute of Fish Culture and Hydrobiology, Zatisi 728/II, 389 25 Vodnany, Czech Republic
  • ,
  • M. Rodina

      Affiliations

    • University of South Bohemia in Ceske Budejovice, Faculty of Fisheries and Protection of Waters, Research Institute of Fish Culture and Hydrobiology, Zatisi 728/II, 389 25 Vodnany, Czech Republic
  • ,
  • D. Gela

      Affiliations

    • University of South Bohemia in Ceske Budejovice, Faculty of Fisheries and Protection of Waters, Research Institute of Fish Culture and Hydrobiology, Zatisi 728/II, 389 25 Vodnany, Czech Republic
  • ,
  • P. Manaskova-Postlerova

      Affiliations

    • Institute of Biotechnology, AS CR, v.v.i., Videnska 1083, 142 20 Prague 4, Czech Republic
  • ,
  • J. Peknicova

      Affiliations

    • Institute of Biotechnology, AS CR, v.v.i., Videnska 1083, 142 20 Prague 4, Czech Republic
  • ,
  • O. Linhart

      Affiliations

    • University of South Bohemia in Ceske Budejovice, Faculty of Fisheries and Protection of Waters, Research Institute of Fish Culture and Hydrobiology, Zatisi 728/II, 389 25 Vodnany, Czech Republic

Received 21 January 2010 ,Revised 23 February 2010 ,Accepted 28 February 2010.

References 

  1. Cabrita E, Alvarez R, Anel L, Rana KJ, Herraez MP. Sublethal damage during cryopreservation of rainbow trout sperm. Cryobiology. 1998;37:245–253
  2. Cao WL, Wang YX, Xiang ZQ, Li Z. Cryopreservation-induced decrease in heat-shock protein 90 in human spermatozoa and its mechanism. Asian J Androl. 2003;5:43–46
  3. Schuffner A, Morshedi M, Oehninger S. Cryopreservation of fractionated, highly motile human spermatozoa: effect on membrane phosphatidylserine externalization and lipid peroxidation. Hum Reprod. 2001;16:2148–2153
  4. Muller P, Erlemann KR, Muller K, Calvete JJ, Topfer-Petersen E, Marienfeld K, et al. Biophysical characterization of the interaction of bovine seminal plasma protein PDC-109 with phospholipid vesicles. Eur Biophys J. 1998;27:33–41
  5. Gadea J, Selles E, Marco MA, Coy P, Matas C, Romar R, et al. Decrease in glutathione content in boar sperm after cryopreservation-Effect of the addition of reduced glutathione to the freezing and thawing extenders. Theriogenology. 2004;62:690–701
  6. Suquet M, Dreanno C, Fauvel C, Cosson J, Billard R. Cryopreservation of sperm in marine fish. Aqua Res. 2000;31:231–243
  7. Lahnsteiner F, Berger B, Horvath A, Urbanyi B. Studies on the semen biology and sperm cryopreservation in the sterlet, Acipenser ruthenus L. Aqua Res. 2004;35:519–528
  8. Zilli L, Schiavone R, Zonno V, Rossano R, Storelli C, Vilella S. Effect of cryopreservation on sea bass sperm proteins. Bio Reprod. 2005;72:1262–1267
  9. Gwo J, Kurokura H, Hirano R. Cryopreservation of spermatozoa from rainbow-trout, common carp, and marine puffer. Nippon suisan gakkaishi. 1993;59:777–782
  10. Horvath A, Miskolui E, Mihalffy S, Osz K, Szabo K, Urbanyi B. Cryopreservation of common carp (Cyprinus carpio) sperm in 1.2 and 5 ml straws and occurrence of haploids among larvae produced with cryopreserved sperm. Cryobiology. 2007;54:251–257
  11. Linhart O, Rodina M, Cosson J. Cryopreservation of sperm in common carp Cyprinus carpio: Sperm motility and hatching success of embryos. Cryobiology. 2000;41:241–250
  12. Warnecke D, Pluta H. Motility and fertilizing capacity of frozen/thawed common carp (Cyprinus carpio L.) sperm using dimethyl-acetamide as the main cryoprotectant. Aquaculture. 2003;215:167–185
  13. McLean L, Young IS, Doherty MK, Robertson DH, Cossins AR, Gracey AY, et al. Global cooling: cold acclimation and the expression of soluble proteins in carp skeletal muscle. Proteomics. 2007;7:2667–2681
  14. Kopeika E. Instruction on low temperature preservation of carp sperm. Moscow: VNIPRKh; 1986;In Russian
  15. Huang SY, Kuo YH, Lee WC, Tsou HL, Lee YP, Chang HL, et al. Substantial decrease of heat-shock protein precedes the decline of sperm motility during cooling of boar spermatozoa. Theriogenology. 1999;51:1007–1016
  16. Lessard C, Parent S, Leclerc P, Bailey JL, Sullivan R. Cryopreservation alters the levels of the bull sperm surface protein P25b. J Andrology. 2000;21:700–707
  17. Burgoyne R, Geisow M. The annexin family of calciumbinding proteins. Cell Calcium. 1989;10:1–10
  18. Warren GH, Marcia AK, Bellamkonda KK, John RD, Mark LZ. Annexin A4 reduces water and proton permeability of model membranes but does not alter aquaporin 2-mediated water transport in isolated endosomes. J Gen Physiol. 2003;121:413–425
  19. Devaux PF. Protein involvement in transmembrane lipid asymmetry. Annu Rev Biophys Biomol Struct. 1992;21:417–439
  20. Hill WG, Zeidel ML. Reconstituting the barrier properties of a water-tight epithelial membrane by design of leaflet specific liposomes. J Biol Chem. 2000;275:30176–30185
  21. Maisse G. Cryopreservation of fish semen: A review. In: Conference of IIR Commission C2 on Refrigeration and Aquaculture. Paris, France: Int Inst Refrigeration; 1996;p. 443–467
  22. Bamburg JR. Proteins of the ADF/cofilin family: essential regulators of actin dynamics. Annu Rev Cell Dev Biol. 1999;15:185–230
  23. Yanagimachi R. Mammalian fertilization. In:  Knobil E,  Neill JD editor. The Physiology of Reproduction. 2nd edition. New York: Raven Press; 1994;p. 189–317
  24. Tomes CN, De Blas GA, Michaut MA, Farre EV, Cherhitin O, Visconti PE, et al. a-SNAP and NSF are required in a priming step during the human sperm acrosome reaction. Molecul Hum Reprod. 2004;11:43–51
  25. Billard R, Cosson J, Crim LW. Motility and survival of halibut sperm during short term storage. Aquat Living Resour. 1993;6:67–75
  26. Palmer JL, Abeles RH. Mechanism of action of S-adenosylhomocysteinase. J Biol Chem. 1979;254:1217–1226
  27. Turner MA, Dole K, Yuan C, Hershfield MS, Borchardt RT, Howell LP. Crystallization and preliminary x-ray analysis of human placental S-adenosylhomocysteine hydrolase. Acta Crystallogr. 1997;D53:339–341
  28. Wojtczak M, Dietrich GJ, Ciereszko A. Transferrin and antiproteases are major proteins of common carp seminal plasma. Fish Shellfish Immun. 2005;19:387–391
  29. Wojtczak M, Dietrich GJ, Irnazarow I, Jurecka P, Słowinska M, Ciereszko A. Polymorphism of transferrin of carp seminal plasma: relationship to blood transferrin and sperm motility characteristics. Comp Biochem Physiol B Biochem Mol Biol. 2007;148:426–431
  30. Chauhan A, Chauhan V, Brown WT, Cohen I. Oxidative stress in autism: increased lipid peroxidation and reduced serum levels of ceruloplasmin and transferrin-the antioxidant proteins. Life Sci. 2004;75:2539–2549
  31. Saleh RA, Agarwal A. Oxidative stress and male infertility: from research bench to clinical practice. J Androl. 2002;23:737–752
  32. Fukuda A, Osawa T, Oda H, Tanaka T, Toyokuni S, Uchida K. Oxidative stress response in iron-induced acute nephrotoxicity: enhanced expression of heat shock protein 90. Biochem Biophys Res Commun. 1996;219:76–81
  33. Satorre MM, Breininger E, Beconi MT, Beorlegui NB. a-Tocopherol modifies tyrosine phosphorylation and capacitation-like state of cryopreserved porcine sperm. Theriogenology. 2007;68:958–965

PII: S0093-691X(10)00139-1

doi: 10.1016/j.theriogenology.2010.02.024

Theriogenology
Volume 74, Issue 3 , Pages 413-423 , August 2010