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Angiopoietin-1 and -2 and vascular endothelial growth factor expression in ovarian grafts after cryopreservation using two methods

  • Cho, In Ae (Department of Obstetrics and Gynecology, Gyeongsang National University Hospital) ;
  • Lee, Yeon Jee (Department of Obstetrics and Gynecology, Gyeongsang National University Hospital) ;
  • Lee, Hee Jung (Department of Obstetrics and Gynecology, Gyeongsang National University Hospital) ;
  • Choi, In Young (Department of Obstetrics and Gynecology, Gyeongsang National University Hospital) ;
  • Shin, Jeong Kyu (Department of Obstetrics and Gynecology, Gyeongsang National University Hospital) ;
  • Lee, Soon Ae (Department of Obstetrics and Gynecology, Gyeongsang National University Hospital) ;
  • Lee, Jong Hak (Department of Obstetrics and Gynecology, Gyeongsang National University Hospital) ;
  • Choi, Won Jun (Department of Obstetrics and Gynecology, Gyeongsang National University Hospital)
  • 투고 : 2018.06.01
  • 심사 : 2018.07.05
  • 발행 : 2018.09.30

초록

Objective: The favored method of preserving fertility in young female cancer survivors is cryopreservation and autotransplantation of ovarian tissue. Reducing hypoxia until angiogenesis takes place is essential for the survival of transplanted ovarian tissue. The aim of this study was to investigate the role of angiopoietin-1 (Angpt-1), angiopoietin-2 (Angpt-2), and vascular endothelial growth factor (VEGF) in ovarian tissue grafts that were cryopreserved using two methods. Methods: Ovarian tissues harvested from ICR mice were divided into three groups: group I (control), no cryopreservation; group II, vitrification in EFS (ethylene-glycol, ficoll, and sucrose solution)-40; and group III, slow freezing in dimethyl sulfoxide. We extracted mRNA for VEGF, Angpt-1, and Angpt-2 from ovarian tissue 1 week following cryopreservation and again 2 weeks after autotransplantation. We used reverse transcriptase-polymerase chain reaction to quantify the levels of VEGF, Angpt-1, and Angpt-2 in the tissue. Results: Angpt-1 and Angpt-2 expression decreased after cryopreservation in groups II and III. After autotransplantation, Angpt-1 and Angpt-2 expression in ovarian tissue showed different trends. Angpt-1 expression in groups II and III was lower than in group I, but Angpt-2 in groups II and III showed no significant difference from group I. The vitrified ovarian tissues had higher expression of VEGF and Angpt-2 than the slow-frozen ovarian tissues, but the difference was not statistically significant. Conclusion: Our results indicate that Angpt-2 may play an important role in ovarian tissue transplantation after cryopreservation although further studies are needed to understand its exact function.

키워드

참고문헌

  1. Donnez J, Martinez-Madrid B, Jadoul P, Van Langendonckt A, Demylle D, Dolmans MM. Ovarian tissue cryopreservation and transplantation: a review. Hum Reprod Update 2006;12:519-35. https://doi.org/10.1093/humupd/dml032
  2. Meirow D, Baum M, Yaron R, Levron J, Hardan I, Schiff E, et al. Ovarian tissue cryopreservation in hematologic malignancy: ten years' experience. Leuk Lymphoma 2007;48:1569-76. https://doi.org/10.1080/10428190701471957
  3. Donnez J, Dolmans MM. Ovarian cortex transplantation: 60 reported live births brings the success and worldwide expansion of the technique towards routine clinical practice. J Assist Reprod Genet 2015;32:1167-70. https://doi.org/10.1007/s10815-015-0544-9
  4. Jensen AK, Macklon KT, Fedder J, Ernst E, Humaidan P, Andersen CY. Erratum to: 86 successful births and 9 ongoing pregnancies worldwide in women transplanted with frozen-thawed ovarian tissue: focus on birth and perinatal outcome in 40 of these children. J Assist Reprod Genet 2017;34:337. https://doi.org/10.1007/s10815-017-0873-y
  5. Sonmezer M, Shamonki MI, Oktay K. Ovarian tissue cryopreservation: benefits and risks. Cell Tissue Res 2005;322:125-32. https://doi.org/10.1007/s00441-005-1098-4
  6. Van den Broecke R, Liu J, Handyside A, Van der Elst JC, Krausz T, Dhont M, et al. Follicular growth in fresh and cryopreserved human ovarian cortical grafts transplanted to immunodeficient mice. Eur J Obstet Gynecol Reprod Biol 2001;97:193-201. https://doi.org/10.1016/S0301-2115(00)00507-8
  7. Bedaiwy MA, Jeremias E, Gurunluoglu R, Hussein MR, Siemianow M, Biscotti C, et al. Restoration of ovarian function after autotransplantation of intact frozen-thawed sheep ovaries with microvascular anastomosis. Fertil Steril 2003;79:594-602. https://doi.org/10.1016/S0015-0282(02)04842-2
  8. Oktay K, Economos K, Kan M, Rucinski J, Veeck L, Rosenwaks Z. Endocrine function and oocyte retrieval after autologous transplantation of ovarian cortical strips to the forearm. JAMA 2001;286:1490-3. https://doi.org/10.1001/jama.286.12.1490
  9. Robinson RS, Woad KJ, Hammond AJ, Laird M, Hunter MG, Mann GE. Angiogenesis and vascular function in the ovary. Reproduction 2009;138:869-81. https://doi.org/10.1530/REP-09-0283
  10. Jeansson M, Gawlik A, Anderson G, Li C, Kerjaschki D, Henkelman M, et al. Angiopoietin-1 is essential in mouse vasculature during development and in response to injury. J Clin Invest 2011;121:2278-89. https://doi.org/10.1172/JCI46322
  11. Fiedler U, Reiss Y, Scharpfenecker M, Grunow V, Koidl S, Thurston G, et al. Angiopoietin-2 sensitizes endothelial cells to TNF-alpha and has a crucial role in the induction of inflammation. Nat Med 2006;12:235-9. https://doi.org/10.1038/nm1351
  12. Joo HJ, Kim H, Park SW, Cho HJ, Kim HS, Lim DS, et al. Angiopoietin-1 promotes endothelial differentiation from embryonic stem cells and induced pluripotent stem cells. Blood 2011;118:2094-104. https://doi.org/10.1182/blood-2010-12-323907
  13. de Vries DK, Khairoun M, Lindeman JH, Bajema IM, de Heer E, Roest M, et al. Renal ischemia-reperfusion induces release of angiopoietin-2 from human grafts of living and deceased donors. Transplantation 2013;96:282-9. https://doi.org/10.1097/TP.0b013e31829854d5
  14. Syrjala SO, Tuuminen R, Nykanen AI, Raissadati A, Dashkevich A, Keranen MA, et al. Angiopoietin-2 inhibition prevents transplant ischemia-reperfusion injury and chronic rejection in rat cardiac allografts. Am J Transplant 2014;14:1096-108. https://doi.org/10.1111/ajt.12672
  15. Lobov IB, Brooks PC, Lang RA. Angiopoietin-2 displays VEGF-dependent modulation of capillary structure and endothelial cell survival in vivo. Proc Natl Acad Sci U S A 2002;99:11205-10. https://doi.org/10.1073/pnas.172161899
  16. Abramovich D, Rodriguez Celin A, Hernandez F, Tesone M, Parborell F. Spatiotemporal analysis of the protein expression of angiogenic factors and their related receptors during folliculogenesis in rats with and without hormonal treatment. Reproduction 2009;137:309-20. https://doi.org/10.1530/REP-08-0130
  17. Choi WJ, Lee JH, Park MH, Choi IY, Park JK, Shin JK, et al. Influence of the vitrification solution on the angiogenic factors in vitrificated mouse ovarian tissue. Obstet Gynecol Sci 2013;56:382-8. https://doi.org/10.5468/ogs.2013.56.6.382
  18. Choi WJ, Seok JS, Choi IY, Park JK, Shin JK, Lee SA, et al. Expression of angiogenic factors in cryopreserved mouse ovaries after heterotopic autotransplantation. Obstet Gynecol Sci 2015;58:391-6. https://doi.org/10.5468/ogs.2015.58.5.391
  19. Kasai M, Komi JH, Takakamo A, Tsudera H, Sakurai T, Machida T. A simple method for mouse embryo cryopreservation in a low toxicity vitrification solution, without appreciable loss of viability. J Reprod Fertil 1990;89:91-7. https://doi.org/10.1530/jrf.0.0890091
  20. Cho HJ, Son WY, Yoon SH, Lee SW, Lim JH. An improved protocol for dilution of cryoprotectants from vitrified human blastocysts. Hum Reprod 2002;17:2419-22. https://doi.org/10.1093/humrep/17.9.2419
  21. Bedaiwy MA, Falcone T. Ovarian tissue banking for cancer patients: reduction of post-transplantation ischaemic injury: intact ovary freezing and transplantation. Hum Reprod 2004;19:1242-4. https://doi.org/10.1093/humrep/deh262
  22. Wang L, Ying YF, Ouyang YL, Wang JF, Xu J. VEGF and bFGF increase survival of xenografted human ovarian tissue in an experimental rabbit model. J Assist Reprod Genet 2013;30:1301-11. https://doi.org/10.1007/s10815-013-0043-9
  23. Mahmoodi M, Soleimani Mehranjani M, Shariatzadeh SM, Eimani H, Shahverdi A. Effects of erythropoietin on ischemia, follicular survival, and ovarian function in ovarian grafts. Reproduction 2014;147:733-41. https://doi.org/10.1530/REP-13-0379
  24. Asahara T, Chen D, Takahashi T, Fujikawa K, Kearney M, Magner M, et al. Tie2 receptor ligands, angiopoietin-1 and angiopoietin-2, modulate VEGF-induced postnatal neovascularization. Circ Res 1998;83:233-40. https://doi.org/10.1161/01.RES.83.3.233
  25. Suri C, Jones PF, Patan S, Bartunkova S, Maisonpierre PC, Davis S, et al. Requisite role of angiopoietin-1, a ligand for the TIE2 receptor, during embryonic angiogenesis. Cell 1996;87:1171-80. https://doi.org/10.1016/S0092-8674(00)81813-9
  26. Youm HW, Lee J, Kim EJ, Kong HS, Lee JR, Suh CS, et al. Effects of angiopoietin-2 on transplanted mouse ovarian tissue. PLoS One 2016;11:e0166782. https://doi.org/10.1371/journal.pone.0166782
  27. Kong HS, Lee J, Youm HW, Kim SK, Lee JR, Suh CS, et al. Effect of treatment with angiopoietin-2 and vascular endothelial growth factor on the quality of xenografted bovine ovarian tissue in mice. PLoS One 2017;12:e0184546. https://doi.org/10.1371/journal.pone.0184546
  28. Brindle NP, Saharinen P, Alitalo K. Signaling and functions of angiopoietin-1 in vascular protection. Circ Res 2006;98:1014-23. https://doi.org/10.1161/01.RES.0000218275.54089.12
  29. Hormozi M, Talebi S, Khorram Khorshid HR, Zarnani AH, Kamali K, Jeddi-Tehrani M, et al. The effect of Setarud (IMOD(TM)) on angiogenesis in transplanted human ovarian tissue to nude mice. Iran J Reprod Med 2015;13:605-14.