期刊论文详细信息
BMC Veterinary Research
Short-term culture of ovarian cortex pieces to assess the cryopreservation outcome in wild felids for genome conservation
Katarina Jewgenow1  Jennifer Zahmel1  Caterina Wiedemann1 
[1] Leibniz Institute for Zoo and Wildlife Research (IZW), PF 700430, Berlin, 10324, Germany
关键词: Primordial follicles;    Ovarian tissue culture;    Ovarian cortex;    Cryopreservation;    Domestic cat;    Wild felids;   
Others  :  1119601
DOI  :  10.1186/1746-6148-9-37
 received in 2012-08-29, accepted in 2013-02-13,  发布年份 2013
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【 摘 要 】

Background

Cryopreservation of ovarian tissue has the potential to preserve female germ cells of endangered mammals. In the present study, a freezing protocol successfully used for human tissue, was adapted for preserving ovarian tissue of domestic and non-domestic felids. Ovaries from non-domestic felid species were obtained from seven freshly euthanized and two recently deceased wild felids kept in different European Zoos. In addition, ovaries from domestic cats were obtained after ovariectomy from local veterinary clinics for methological adaptations.

Ovarian cortex was dissected and uniform sized pieces of 2 mm diameter were obtained. Using a slow freezing protocol (-0.3°C per min) in 1.5 mol/L ethylene glycol, 0.1 mol/L sucrose, the pieces were cultured for up to 14 days both before and after cryopreservation. The integrity of primordial follicles was assessed by histology, and the impact of different protein sources (FCS or BSA) and Vitamin C was determined during two weeks of culture.

Results and conclusion

During culture the number of primordial follicles decreased within the ovarian pieces (p < 0.05). This effect was less pronounced when FCS was used as the protein source instead of BSA. Supplementation with Vitamin C had a detrimental effect on follicle survival. Since the procedure of cryopreservation had no effect on the follicle survival after one week of culture we conclude that the freezing protocol was suitable for felids. This is the first report of preserving a huge amount of follicles within ovarian tissue by slow freezing performed in several wild feline species.

【 授权许可】

   
2013 Wiedemann et al.; licensee BioMed Central Ltd.

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【 参考文献 】
  • [1]The Red List of IUCN. http://www.iucn.org/about/work/programmes/species/our_work/the_iucn_red_list/ webcite
  • [2]Convention on International Trade in Endangered Species of Wild Fauna and Flora. http://www.cites.org/ webcite
  • [3]Lermen D, Blomeke B, Browne R, Clarke A, Dyce PW, Fixemer T, Fuhr GR, Holt WV, Jewgenow K, Lloyd RE: Cryobanking of viable biomaterials: implementation of new strategies for conservation purposes. Mol Ecol 2009, 18(6):1030-1033.
  • [4]Holt WV, Bennett PM, Volobouev V, Watson PF: Genetic resource banks in wildlife conservation. J Zool 1996, 238:531-544.
  • [5]Wildt DE: Genetic resource banks for conserving wildlife species – justification, examples and becoming organized on a global basis. Anim Reprod Sci 1992, 28:247-257.
  • [6]Jewgenow K, Wiedemann C, Bertelsen MF, Ringleb J: Cryopreservation of mammalian oocytes and ovaries. Int Zoo Year 2011, 45:124-132.
  • [7]Shaw JM, Trounson AO: Experimental models for ovarian tissue and immature follicles. Semin Reprod Med 2002, 20(1):51-62.
  • [8]Jewgenow K, Paris MC: Preservation of female germ cells from ovaries of cat species. Theriogenology 2006, 66(1):93-100.
  • [9]Andersen CY, Silber SJ, Berghold SH, Jorgensen JS, Ernst E: Long-term duration of function of ovarian tissue transplants: case reports. Reprod Biomed Online 2012, 25(2):128-132.
  • [10]Andersen CY, Kristensen SG, Greve T, Schmidt KT: Cryopreservation of ovarian tissue for fertility preservation in young female oncological patients. Future Oncol 2012, 8(5):595-608.
  • [11]Gunasena KT, Villines PM, Critser ES, Critser JK: Live births after autologous transplant of cryopreserved mouse ovaries. Hum Reprod 1997, 12(1):101-106.
  • [12]Santos RR, Knijn HM, Vos PL, Oei CH, van Loon T, Colenbrander B, Gadella BM, van den Hurk R, Roelen BA: Complete follicular development and recovery of ovarian function of frozen-thawed, autotransplanted caprine ovarian cortex. Fertil Steril 2009, 91(4 Suppl):1455-1458.
  • [13]Gosden RG, Baird DT, Wade JC, Webb R: Restoration of fertility to oophorectomized sheep by ovarian autografts stored at -196°C. Hum Reprod 1994, 9(4):597-603.
  • [14]Bosch P, Hernandez-Fonseca HJ, Miller DM, Wininger JD, Massey JB, Lamb SV, Brackett BG: Development of antral follicles in cryopreserved cat ovarian tissue transplanted to immunodeficient mice. Theriogenology 2004, 61(2–3):581-594.
  • [15]Fassbender M, Hildebrandt TB, Paris MC, Colenbrander B, Jewgenow K: High-resolution ultrasonography of xenografted domestic cat ovarian cortex. J Reprod Dev 2007, 53(5):1023-1034.
  • [16]Kvist K, Thorup J, Byskov AG, Hoyer PE, Mollgard K, Yding Andersen C: Cryopreservation of intact testicular tissue from boys with cryptorchidism. Hum Reprod 2006, 21(2):484-491.
  • [17]Telfer EE, McLaughlin M, Ding C, Thong KJ: A two-step serum-free culture system supports development of human oocytes from primordial follicles in the presence of activin. Hum Reprod 2008, 23(5):1151-1158.
  • [18]Abercrombie M: Estimation of nuclear population from microtome sections. Anat Rec 1946, 94:239-247.
  • [19]Lima AK, Silva AR, Santos RR, Sales DM, Evangelista AF, Figueiredo JR, Silva LD: Cryopreservation of preantral ovarian follicles in situ from domestic cats (Felis catus) using different cryoprotective agents. Theriogenology 2006, 66(6–7):1664-1666.
  • [20]Luvoni GC, Tessaro I, Apparicio M, Ruggeri E, Luciano AM, Modina SC: Effect of vitrification of feline ovarian cortex on follicular and oocyte quality and competence. Reprod Domest Anim 2011, 47(3):385-391.
  • [21]Jewgenow K: Role of media, protein and energy supplements on maintenance of morphology and DNA-synthesis of small preantral domestic cat follicles during short-term culture. Theriogenology 1998, 49(8):1567-1577.
  • [22]Poschmann M, Fassbender M, Lopes C, Dorresteijn A, Jewgenow K: Viability assessment of primordial follicles of domestic cats to develop cryopreservation protocols for ovarian tissue. Reprod Domest Anim 2008, 43:25-25.
  • [23]Isachenko V, Montag M, Isachenko E, van der Ven K, Dorn C, Roesing B, Braun F, Sadek F, van der Ven H: Effective method for in-vitro culture of cryopreserved human ovarian tissue. Reprod Biomed Online 2006, 13(2):228-234.
  • [24]Wandji SA, Srsen V, Voss AK, Eppig JJ, Fortune JE: Initiation in vitro of growth of bovine primordial follicles. Biol Reprod 1996, 55(5):942-948.
  • [25]Wandji SA, Srsen V, Nathanielsz PW, Eppig JJ, Fortune JE: Initiation of growth of baboon primordial follicles in vitro. Hum Reprod 1997, 12(9):1993-2001.
  • [26]Hovatta O, Silye R, Abir R, Krausz T, Winston RM: Extracellular matrix improves survival of both stored and fresh human primordial and primary ovarian follicles in long-term culture. Hum Reprod 1997, 12(5):1032-1036.
  • [27]Matos MH, Lima-Verde IB, Bruno JB, Lopes CA, Martins FS, Santos KD, Rocha RM, Silva JR, Bao SN, Figueiredo JR: Follicle stimulating hormone and fibroblast growth factor-2 interact and promote goat primordial follicle development in vitro. Reprod Fertil Dev 2007, 19(5):677-684.
  • [28]Wright CS, Hovatta O, Margara R, Trew G, Winston RM, Franks S, Hardy K: Effects of follicle-stimulating hormone and serum substitution on the in-vitro growth of human ovarian follicles. Hum Reprod 1999, 14(6):1555-1562.
  • [29]Qureshi AI, Nussey SS, Bano G, Musonda P, Whitehead SA, Mason HD: Testosterone selectively increases primary follicles in ovarian cortex grafted onto embryonic chick membranes: relevance to polycystic ovaries. Reproduction 2008, 136(2):187-194.
  • [30]Yang MY, Fortune JE: Testosterone stimulates the primary to secondary follicle transition in bovine follicles in vitro. Biol Reprod 2006, 75(6):924-932.
  • [31]Wood TC, Byers AP, Jennette BE, Wildt DE: Influence of protein and hormone supplementation on in vitro maturation and fertilization of domestic cat eggs. J Reprod Fertil 1995, 104(2):315-323.
  • [32]Rossetto R, Lima-Verde IB, Matos MH, Saraiva MV, Martins FS, Faustino LR, Araujo VR, Silva CM, Name KP, Sn SN: Interaction between ascorbic acid and follicle-stimulating hormone maintains follicular viability after long-term in vitro culture of caprine preantral follicles. Domest Anim Endocrinol 2009, 37(2):112-123.
  • [33]Murray AA, Molinek MD, Baker SJ, Kojima FN, Smith MF, Hillier SG, Spears N: Role of ascorbic acid in promoting follicle integrity and survival in intact mouse ovarian follicles in vitro. Reproduction 2001, 121(1):89-96.
  • [34]Thomas FH, Leask R, Srsen V, Riley SC, Spears N, Telfer EE: Effect of ascorbic acid on health and morphology of bovine preantral follicles during long-term culture. Reproduction 2001, 122(3):487-495.
  • [35]Mortola E, Okuda M, Ohno K, Watari T, Tsujimoto H, Hasegawa A: Inhibition of apoptosis and virus replication in feline immunodeficiency virus-infected cells by N-acetylcysteine and ascorbic acid. J Vet Med Sci 1998, 60(11):1187-1193.
  • [36]Viviano KR, Lavergne SN, Goodman L, Vanderwielen B, Grundahl L, Padilla M, Trepanier LA: Glutathione, cysteine, and ascorbate concentrations in clinically ill dogs and cats. J Vet Intern Med 2009, 23(2):250-257.
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