Human oocyte vitrification with corona radiata, in autologous follicular fluid supplemented with ethylene glycol, preserves conventional IVF potential: birth of four healthy babies
Xian-Hong Tong A B , Li-Min Wu B , Ren-Tao Jin B , Hong-Bing Luan B and Yu-Sheng Liu B CA Institute of Immunology, Medical College of Shandong University, Jinan 250012, China.
B Reproductive Medical Centre of Anhui Provincial Hospital Affiliated to Anhui Medical University, Hefei 230001, China.
C Corresponding author. Email: shengzhizhongxin@126.com
Reproduction, Fertility and Development 26(7) 1001-1006 https://doi.org/10.1071/RD13161
Submitted: 25 May 2013 Accepted: 28 June 2013 Published: 5 August 2013
Abstract
The aim of this study was to examine the effects of vitrification with autologous follicular fluid (AFF) supplemented with ethylene glycol (EG) and sucrose on human oocytes with corona radiata. A total of 182 human oocytes with corona radiata from fifteen infertile patients were vitrified using either equilibration solutions (ES) and vitrification solution (VS) consisting of AFF, EG and sucrose (AFF group, n = 67) or commercial ES and VS (control group, n = 115). All oocytes were thawed in the next cycle, with surviving oocytes being inseminated by conventional IVF. The clinical outcome of vitrified–warmed oocytes by both vitrification methods was analysed retrospectively. In the AFF group, six patients received embryo transfer, with three couples taking four healthy babies home. In the control group, nine patients received embryo transfer, with four couples taking five healthy babies home. There was no significant difference in the survival rate (91.0 vs 92.2%), two pronuclei (2PN) fertilisation rate (73.8 vs 73.6%), cleavage rate (100 vs 100%), top-quality embryo rate (62.2 vs 59.2%), clinical pregnancy rate (50.0 vs 44.4%), implantation rate (33.3 vs 25%) or take-home baby rate (50.0 vs 44.4%) between the AFF group and the control group, respectively. These results show that AFF supplemented with EG and sucrose is an efficient, cost-effective cryoprotectant for human oocyte cryopreservation. A corona radiata on vitrified–warmed oocytes retains the oocytes’ fertilisation capability in conventional IVF.
Additional keywords: cryopreservation, cumulus cells, fertilisation, Open Pulled Straw (OPS), take home baby rate.
References
Coticchio, G., Bonu, M. A., Sciajno, R., Sereni, E., Bianchi, V., and Borini, A. (2007). Truths and myths of oocyte sensitivity to controlled rate freezing. Reprod. Biomed. Online 15, 24–30.| Truths and myths of oocyte sensitivity to controlled rate freezing.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BD2svgsFagtg%3D%3D&md5=2e7cf152a4c012fbfd4124016539c68bCAS | 17623530PubMed |
Ghetler, Y., Skutelsky, E., Ben Nun, I., Ben Dor, L., Amihai, D., and Shalgi, R. (2006). Human oocyte cryopreservation and the fate of cortical granules. Fertil. Steril. 86, 210–216.
| Human oocyte cryopreservation and the fate of cortical granules.Crossref | GoogleScholarGoogle Scholar | 16756978PubMed |
Gook, D. A., and Edgar, D. H. (2007). Human oocyte cryopreservation. Hum. Reprod. Update 13, 591–605.
| Human oocyte cryopreservation.Crossref | GoogleScholarGoogle Scholar | 17846105PubMed |
Grupen, C. G., and Armstrong, D. T. (2010). Relationship between cumulus cell apoptosis, progesterone production and porcine oocyte developmental competence: temporal effects of follicular fluid during IVM. Reprod. Fertil. Dev. 22, 1100–1109.
| Relationship between cumulus cell apoptosis, progesterone production and porcine oocyte developmental competence: temporal effects of follicular fluid during IVM.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXhtVOgu7vN&md5=1852eef0ffa8cef12e7a50b30c403e80CAS | 20797348PubMed |
Imoedemhe, D. G., and Sigue, A. B. (1992). Survival of human oocytes cryopreserved with or without the cumulus in 1,2-propanediol. J. Assist. Reprod. Genet. 9, 323–327.
| Survival of human oocytes cryopreserved with or without the cumulus in 1,2-propanediol.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DyaK3s7htlWmtQ%3D%3D&md5=bff8f2548a5c964ac62b20805d1316a2CAS | 1472809PubMed |
Józwik, M., Józwik, M., Teng, C., and Battaglia, F. C. (2006). Amino acid, ammonia and urea concentrations in human pre-ovulatory ovarian follicular fluid. Hum. Reprod. 21, 2776–2782.
| Amino acid, ammonia and urea concentrations in human pre-ovulatory ovarian follicular fluid.Crossref | GoogleScholarGoogle Scholar | 16950828PubMed |
Józwik, M., Józwik, M., Teng, C., and Battaglia, F. C. (2007). Concentrations of monosaccharides and their amino and alcohol derivatives in human preovulatory follicular fluid. Mol. Hum. Reprod. 13, 791–796.
| Concentrations of monosaccharides and their amino and alcohol derivatives in human preovulatory follicular fluid.Crossref | GoogleScholarGoogle Scholar | 17766681PubMed |
Kohaya, N., Fujiwara, K., Ito, J., and Kashiwazaki, N. (2011). High developmental rates of mouse oocytes cryopreserved by an optimized vitrification protocol: the effects of cryoprotectants, calcium and cumulus cells. J. Reprod. Dev. 57, 675–680.
| High developmental rates of mouse oocytes cryopreserved by an optimized vitrification protocol: the effects of cryoprotectants, calcium and cumulus cells.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38XjtVGrsLk%3D&md5=0ab0ea1702df80665fb41b35f0c016dbCAS | 21778666PubMed |
Lagares, M. A., Castanheira, P. N., Amaral, D. C., Vasconcelos, A. B., Veado, J. C., Arantes, R. M., and Stahlberg, R. (2009). Addition of ficoll and disaccharides to vitrification solutions improve in vitro viability of vitrified equine embryo. Cryo Letters 30, 408–413.
| 1:CAS:528:DC%2BC3cXks1Srs74%3D&md5=873d377c0e6be441939ca09a866e02aaCAS | 20309496PubMed |
Park, S. E., Chung, H. M., Cha, K. Y., Hwang, W. S., Lee, E. S., and Lim, J. M. (2001). Cryopreservation of ICR mouse oocytes: improved post-thawed preimplantation development after vitrification using Taxol, a cytoskeleton stabilizer. Fertil. Steril. 75, 1177–1184.
| Cryopreservation of ICR mouse oocytes: improved post-thawed preimplantation development after vitrification using Taxol, a cytoskeleton stabilizer.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BD3MzhtFymug%3D%3D&md5=e594bcdee8b7db8ade931491d7d67910CAS | 11384646PubMed |
Popelková, M., Turanová, Z., Koprdová, L., Ostró, A., Toporcerová, S., Makarevich, A. V., and Chrenek, P. (2009). Effect of vitrification technique and assisted hatching on rabbit embryo developmental rate. Zygote 17, 57–61.
| Effect of vitrification technique and assisted hatching on rabbit embryo developmental rate.Crossref | GoogleScholarGoogle Scholar | 19032802PubMed |
Santiquet, N. W., Develle, Y., Laroche, A., Robert, C., and Richard, F. J. (2012). Regulation of gap-junctional communication between cumulus cells during in vitro maturation in swine, a gap-FRAP study. Biol. Reprod. 87, 46.
| Regulation of gap-junctional communication between cumulus cells during in vitro maturation in swine, a gap-FRAP study.Crossref | GoogleScholarGoogle Scholar | 22649071PubMed |
Tadashi, M., Tomoko, A., and Hiroshi, S. (2000). Roles of gap junctional communication of cumulus cells in cytoplasmic maturation of porcine oocytes cultured in vitro. Biol. Reprod. 62, 913–919.
| Roles of gap junctional communication of cumulus cells in cytoplasmic maturation of porcine oocytes cultured in vitro.Crossref | GoogleScholarGoogle Scholar |
Tharasanit, T., Colleoni, S., Galli, C., Colenbrander, B., and Stout, T. A. (2009). Protective effects of the cumulus–corona radiata complex during vitrification of horse oocytes. Reproduction 137, 391–401.
| Protective effects of the cumulus–corona radiata complex during vitrification of horse oocytes.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXovV2ksbo%3D&md5=3b5ea55f2b364b15acc06c34f98868bdCAS | 19073713PubMed |
Tong, X. H., Wu, L. M., Jin, R. T., Luo, L. H., Luan, H. B., and Liu, Y. S. (2012). Fertilization rates are improved after IVF if the corona radiata is left intact in vitrified–warmed human oocytes. Hum. Reprod. 27, 3208–3214.
| Fertilization rates are improved after IVF if the corona radiata is left intact in vitrified–warmed human oocytes.Crossref | GoogleScholarGoogle Scholar | 22926844PubMed |
Vajta, G., Holm, P., Kuwayama, M., Booth, P. J., Jacobsen, H., Greve, T., and Callesen, H. (1998). Open pulled straw (OPS) vitrification: a new way to reduce cryoinjuries of bovine ova and embryos. Mol. Reprod. Dev. 51, 53–58.
| Open pulled straw (OPS) vitrification: a new way to reduce cryoinjuries of bovine ova and embryos.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK1cXltVGrs7g%3D&md5=49d4e9194babffb16608d70dd43f2acdCAS | 9712317PubMed |
Vergouw, C. G., Botros, L. L., Roos, P., Lens, J. W., Schats, R., Hompes, P. G. A., Burns, D. H., and Lambalk, C. B. (2008). Metabolomic profiling by near-infrared spectroscopy as a tool to assess embryo viability: a novel, non-invasive method for embryo selection. Hum. Reprod. 23, 1499–1504.
| Metabolomic profiling by near-infrared spectroscopy as a tool to assess embryo viability: a novel, non-invasive method for embryo selection.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXmvFWgtr4%3D&md5=88e99a18413a3dc294cbdef25b24da32CAS | 18424459PubMed |
Zhang, L., Jiang, S., Wozniak, P. J., Yang, X., and Godke, R. A. (1995). Cumulus cell function during bovine oocyte maturation, fertilization and embryo development in vitro. Mol. Reprod. Dev. 40, 338–344.
| Cumulus cell function during bovine oocyte maturation, fertilization and embryo development in vitro.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK2MXkt1Khs7k%3D&md5=5c8bcb7377b1883ec1f1fcb8d3ef8094CAS | 7772344PubMed |