The comparison of developed mouse vitrified preantral follicle with isolated preantral follicles from vitrified ovary

authors:

avatar Elmira Hosseinzade , avatar saeed zavareh , * , avatar Taghi Lashkarboluki

Koomesh: Vol.17, issue 4; 981-989
article type: issue_documents_importer
received: March 01, 2015
accepted: December 03, 2015

how to cite: Hosseinzade E, zavareh S, Lashkarboluki T. The comparison of developed mouse vitrified preantral follicle with isolated preantral follicles from vitrified ovary. koomesh. 2024;17(4):e151193. 

Abstract

Introduction: Cryopreservation techniques are useful methods for long-term storage of cells and tissues of the reproductive system. The purpose of this study was to investigate the development and survival rate of vitrified preantral follicles compare with those of isolated preantral follicles from vitrified ovaries. Materials and methods: Preantral follicles of 14 to 16 days-old of NMRI mice ovaries were randomly divided into three groups. Group I: preantral follicles derived from fresh ovaries (control). Group II: preantral follicles derived from vitrified ovaries and group 3: vitrified preantral follicles. After thawing, preantral follicles were cultured in α- MEM medium containing 5% FBS, 100 mIU/ml hFSH, 1% ITS and 10 ng/ ml EGF.  At the day 12 of culture, ovulation was induced by adding 1.5 IU/ml hCG. The preantral follicle diameter and the rates of survival, antrum formation and developmental stages of released oocytes were evaluated. Results: The results showed that the survival rate of vitrified preantral follicles was significantly higher than that of isolated preantral follicle from vitrified ovaries. The mean diameter of preantral follicles, the rates of antrum formation and MII stage oocytes in vitrified preantral follicles were significantly higher than those of isolated preantral follicles from vitrified ovaries. Conclusion: Vitrified preantral follicles were more suitable to develop to mature oocytes in comparison with isolated preantral follicles from vitrified ovaries.

References

  • 1.

    Porcu E, Fabbri R, Seracchioli R, Ciotti PM, Magrini O, Flamigni C. Birth of a healthy female after intracytoplasmic sperm injection of cryopreserved human oocytes. Fertil Steril 1997; 68: 724-726.

  • 2.

    Choi J, Lee B, Lee E, Yoon BK, Bae D, Choi D. Cryopreservation of ovarian tissues temporarily suppresses the proliferation of granulosa cells in mouse preantral follicles. Cryobiology 2008; 56: 36-42.

  • 3.

    Choi J, Lee Jy, Lee E, Yoon BK, Bae D, Choi D. Cryopreservation of the mouse ovary inhibits the onset of primordial follicle development. Cryobiology 2007; 54: 55-62.

  • 4.

    Choi WJ, Yeo HJ, Shin JK, Lee S, Lee JH, Paik WY. Effect of vitrification method on survivability, follicular growth and ovulation of preantral follicles in mice. J Obstet Gynaecology Res 2007; 33: 128-133.

  • 5.

    Amorim CA, Gonalves PB, Figueiredo JR. Cryopreservation of oocytes from pre-antral follicles. Hum Reprod Update 2003; 9: 119-129.

  • 6.

    Son WY, Yoon SH, Park SJ, Yoon HJ, Lee WD, Lim JH. Ongoing twin pregnancy after vitrification of blastocysts produced by in-vitro matured oocytes retrieved from a woman with polycystic ovary syndrome: case report. Human Reprod 2002; 17: 2963-2966.

  • 7.

    Mathias FJ, D'Souza F, Uppangala S, Salian SR, Kalthur G, Adiga SK. Ovarian tissue vitrification is more efficient than slow freezing in protecting oocyte and granulosa cell DNA integrity. Syst Biol Reprod Med 2014; 60: 317-322.

  • 8.

    Kagabu S, Umezu M. Transplantation of cryopreserved mouse, Chinese hamster, rabbit, Japanese monkey and rat ovaries into rat recipients. Exp Anim 2000; 49: 17-21.

  • 9.

    Pegg D. The current status of tissue cryopreservation. Cryo Lett 2000; 22: 105-114.

  • 10.

    Isachenko V, Isachenko E, Rahimi G, Krivokharchenko A, Alabart J, Nawroth F. Cryopreservation of human ovarian tissue by direct plunging into liquid nitrogen: negative effect of disaccharides in vitrification solution. Cryo Lett 2002; 23: 333-344.

  • 11.

    Oktay K, Karlikaya GG, Aydin BA. Ovarian cryopreservation and transplantation: basic aspects. Mol Cell Endocrinol 2000; 169: 105-108.

  • 12.

    Oktay K, Oktem O. Ovarian cryopreservation and transplantation for fertility preservation for medical indications: report of an ongoing experience. Fertil Steril 2010; 93: 762-768.

  • 13.

    Shaw J, Cox S-L, Trounson A, Jenkin G. Evaluation of the long-term function of cryopreserved ovarian grafts in the mouse, implications for human applications. Mol Cell Endocrinol 2000; 161: 103-110.

  • 14.

    Shaw J, Oranratnachai A, Trounson A. Fundamental cryobiology of mammalian oocytes and ovarian tissue. Theriogenology 2000; 53: 59-72.

  • 15.

    Shaw JM, Bowles J, Koopman P, Wood EC, Trounson AO. Fresh and cryopreserved ovarian tissue samples from donors with lymphoma transmit the cancer to graft recipients. Hum Reprod 1996; 11: 1668-1673.

  • 16.

    Demeestere I, Simon P, Emiliani S, Delbaere A, Englert Y. Fertility preservation: successful transplantation of cryopreserved ovarian tissue in a young patient previously treated for Hodgkin's disease. The Oncologist 2007; 12: 1437-1442.

  • 17.

    Paynter S, Cooper A, Fuller B, Shaw R. Cryopreservation of bovine ovarian tissue: structural normality of follicles after thawing and culturein vitro. Cryobiology 1999; 38: 301-309.

  • 18.

    Salle B, Demirci B, Franck M, Berthollet C, Lornage J. Long-term follow-up of cryopreserved hemi-ovary autografts in ewes: pregnancies, births, and histologic assessment. Fertil Steril 2003; 80: 172-177.

  • 19.

    Silber S, DeRosa M, Pineda Je, Lenahan K, Grenia D, Gorman K, Gosden R. A series of monozygotic twins discordant for ovarian failure: ovary transplantation (cortical versus microvascular) and cryopreservation. Hum Reprod 2008; 23: 1531-1537.

  • 20.

    Chen SU, Chien CL, Wu MY, Chen TH, Lai SM, Lin CW, Yang YS. Novel direct cover vitrification for cryopreservation of ovarian tissues increases follicle viability and pregnancy capability in mice. Hum Reprod 2006; 21: 2794-2800.

  • 21.

    Kuwayama M. Highly efficient vitrification for cryopreservation of human oocytes and embryos: the Cryotop method. Theriogenology 2007; 67: 73-80.

  • 22.

    Abedelahi A, Salehnia M, Allameh AA, Davoodi D. Sodium selenite improves the in vitro follicular development by reducing the reactive oxygen species level and increasing the total antioxidant capacity and glutathione peroxide activity. Hum Reprod 2010; 25: 977-985.

  • 23.

    Gook DA, Edgar D, Stern C. Cryopreservation of human ovarian tissue. Eur J Obstet Gynecol Reprod Biol 2004; 113: S41-S44.

  • 24.

    Gook DA, Edgar D, Stern C. The effects of cryopreservation regimens on the morphology of human ovarian tissue. Mol Cell Endocrinol 2000; 169: 99-103.

  • 25.

    Eimani H, Behbahanian A, Zeinali B, Valoujerdi MR, Eftekhari P, Shahverdi A, et al. Heterotopic autotransplantation of vitrified mouse ovary. Reprod Med Biol 2011; 10: 267-275.

  • 26.

    Kim SS, Battaglia DE, Soules MR. The future of human ovarian cryopreservation and transplantation: fertility and beyond. Fertil Steril 2001; 75: 1049-1056.

  • 27.

    Kim SS, Yang HW, Kang HG, Lee HH, Lee HC, Ko DS, Gosden RG. Quantitative assessment of ischemic tissue damage in ovarian cortical tissue with or without antioxidant (ascorbic acid) treatment. Fertil Steril 2004; 82: 679-685.

  • 28.

    Dahl SL, Chen Z, Solan AK, Brockbank KG, Niklason LE, Song YC. Feasibility of vitrification as a storage method for tissue-engineered blood vessels. Tissue Eng 2006; 12: 291-300.

  • 29.

    Rahimi G, Isachenko E, Sauer H, Isachenko V, Wartenberg M, Hescheler J, et al. Effect of different vitrification protocols for human ovarian tissue on reactive oxygen species and apoptosis. Reprod Fertil Dev 2003; 15: 343-349.

  • 30.

    Hatami S, Zavareh S, Salehnia M, Lashkarbolouki T, Ghorbanian MT, Karimi I. The impact of alpha lipoic acid on developmental competence of mouse vitrified pre-antral follicles in comparison to those isolated from vitrified ovaries. Iranian J Reprod Med 2014; 12: 57.

  • 31.

    Wang LY, Wang DH, Zou XY, Xu CM. Mitochondrial functions on oocytes and preimplantation embryos. J Zhejiang Univ Sci B 2009; 10: 483-492.

  • 32.

    De los Reyes M, Palomino J, Parraguez VH, Hidalgo M, Saffie P. Mitochondrial distribution and meiotic progression in canine oocytes during in vivo and in vitro maturation. Theriogenology 2011; 75: 346-353.

  • 33.

    Brenner CA, Kubisch HM, Pierce KE. Role of the mitochondrial genome in assisted reproductive technologies and embryonic stem cell-based therapeutic cloning. Reprod Fertil Dev 2004; 16: 743-751.

  • 34.

    Nagai S, Mabuchi T, Hirata S, Shoda T, Kasai T, Yokota S, et al. Correlation of abnormal mitochondrial distribution in mouse oocytes with reduced developmental competence. Tohoku J Exp Med 2006; 210: 137-144.

  • 35.

    Wang AW, Zhang H, Ikemoto I, Anderson DJ, Loughlin KR. Reactive oxygen species generation by seminal cells during cryopreservation. Urology 1997; 49: 921-925.

  • 36.

    Taghavi A, Voloojerdi R, Foroozandeh M. Comparison of apoptosis, viability and maturation in mouse preantral follicle after slow freezing and cryotop vitrification. Tehran Tarbiat Modares 2009. (Persian).

  • 37.

    Huang L, Mo Y, Wang W, Li Y, Zhang Q, Yang D. Cryopreservation of human ovarian tissue by solid-surface vitrification. Eur J Obstet Gynecol Reprod Biol 2008; 139: 193-198.

  • 38.

    Fuller B, Paynter S. Fundamentals of cryobiology in reproductive medicine. Reprod Biomed Online 2004; 9: 680-691.