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2020 | 76 | 03 |

Tytuł artykułu

Piglets produced by transfer of embryos obtained by in vitro fertilization of oocytes matured in vitro with thymosin: a case report

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
The aim of the study was to examine the in vivo viability of in vitro-produced (IVP) porcine embryos obtained from oocytes matured with thymosin. The research material for this study consisted of immature pig oocytes obtained from ovaries after slaughter and ejaculated semen obtained from one boar. The immature oocytes were cultured in vitro until the metaphase II stage in a medium supplemented with thymosin (TMS). The presumptive zygotes obtained were cultured in vitro for 4-40 hours. The presumptive zygotes and 2-4-cell embryos were evaluated in vivo after transferring them to synchronized recipients. After the transfer of embryos from the experimental group into 2 recipients (50 embryos into each gilt) and the transfer of 50 embryos from the control group into 1 recipient, both gilts that had received embryos obtained by in vitro fertilization of oocytes matured with TMS became pregnant and delivered a total of 16 live piglets. After the transfer of embryos from the control group, no pregnancy was achieved. In conclusion, the results of our preliminary study suggest that the maturation of pig oocytes with thymosin supports the in vivo survival of in vitro produced embryos. It is important to note, that this was the first birth of piglets obtained after transfer of IVP embryos in Poland.

Słowa kluczowe

Wydawca

-

Rocznik

Tom

76

Numer

03

Opis fizyczny

p.181-185,fig.,ref.

Twórcy

  • Department of Reproductive Biotechnology and Cryopreservation, National Research Institute of Animal Production, 32-083 Balice-Krakow, Poland
autor
  • Department of Reproductive Biotechnology and Cryopreservation, National Research Institute of Animal Production, 32-083 Balice-Krakow, Poland
autor
  • Department of Reproductive Biotechnology and Cryopreservation, National Research Institute of Animal Production, 32-083 Balice-Krakow, Poland
autor
  • Department of Reproductive Biotechnology and Cryopreservation, National Research Institute of Animal Production, 32-083 Balice-Krakow, Poland
autor
  • Department of Reproductive Biotechnology and Cryopreservation, National Research Institute of Animal Production, 32-083 Balice-Krakow, Poland

Bibliografia

  • Batista R. I., Moro L. N., Corbin E., Alminana C., Gonҫalves Souza-Fabian J. M., de Figueirȇdo Freitas V. J., Mermillod P.: Combination of oviduct fluid and heparin to improve monospermic zygotes production during porcine in vitro fertilization. Theriogenology 2016, 86, 495-502.
  • Beckmann L. S., Day B. N.: Effects of media NaCl concentration and osmolarity on the culture of early-stage porcine embryos and the viability of embryos cultured in a selected superior medium. Theriogenology 1993, 39, 611-622.
  • Bock-Marquette I., Saxena A., White M. D., DiMaio J. M., Srivastava D.: Thymosin β4 activates integrin-linked kinase and promotes cardiac cell migration, survival and cardiac repair. Nature 2004, 432, 7016, 466-472.
  • Brüssow K. P., Rátky J., Antosik P., Kempisty B., Jaśkowski J. M.: An indispensable key for the application of reproductive technique. EJPAU 2018, 21, 1-6.
  • Cheng W. T. K., Polge C., Moor R. M.: In vitro fertilization of pig and sheep oocytes. Theriogenology 1986, 25, 146 (abstract).
  • Dobrinsky J. R., Johnson L. A., Rath D.: Development of a culture medium (BECM-3) for porcine embryos: effects of bovine serum albumin and fetal bovine serum on embryo development. Biol. Reprod. 1996, 55, 1069-1074.
  • Ford J. J., Vakharia D. D., Anderson L. L., Klindt J.: Thymosin-beta 4 concentrations during the estrous cycle and after hypophyseal stalk transection of female pigs. Proc. Soc. Exp. Biol. Med. 1990, 193, 185-189.
  • Fowler K. E., Mandawala A. A., Griffin D. K., Walling G. A., Harvey S. C.: The production of pig preimplantation embryos in vitro: Current progress and future prospects. Reprod. Biol. 2018, 18, 203-211.
  • Gajda B., Poniedziałek-Kempny K., Rajska I., Smorąg Z.: Effect of thymosin on in vitro fertilization and developmental competence and quality of pig embryos. Proc. 31st Meeting AETE, Ghent, Belgium, Animal. Reprod. 2015, 12, 735.
  • Gajda B., Poniedziałek-Kempny K., Rajska I., Smorąg Z.: Wpływ tymozyny na dojrzewanie in vitro oocytów świni. Proc. LXXIX Zjazd Naukowy PTZ, Siedlce 15-17 września 2014, p. 125.
  • Gajda B., Smorąg Z.: Kriokonserwacja oocytów i zarodków świni – aspekty biologiczne i biotechnologiczne. Ośrodek Wydawnictw Naukowych, Poznań 2013, p. 130.
  • Gil M. A., Nohalez A., Martinez C. A., Ake-Villanueva J. R., Centurion-Castro F., Maside C., Cuello C., Roca J., Parrilla I., Martinez E. A.: Effects of meiotic inhibitors and gonadotrophins on porcine oocytes in vitro maturation, fertilization and development. Reprod. Domest. Anim. 2017, 52, 873-880.
  • Hara T.: Thymosins and muscle regeneration. Vitam. Horm. 2011, 87, 277-286.
  • Lee S., Jin J. X., Khoirinaya C., Kim G. A., Lee B. C.: Lanosterol influences cytoplasmic maturation of pig oocytes in vitro and improves preimplantation development of cloned embryos. Theriogenology 2016, 85, 575-584.
  • Lee S., Jin J. X., Taweechaipaisankul A., Kim G. A., Lee B. Ch.: Synergistic effect of resveratrol and melatonin on in vitro maturation of porcine oocytes and subsequent embryo development. Theriogenology 2018, 114, 191-198.
  • Liang S., Guo J., Jin Y. X., Yuan B., Zhang J. B., Kim N. H.: C-Phycocyanin supplementation during in vitro maturation enhances pre-implantation developmental competence of parthenogenetic and cloned embryos in pigs. Theriogenology 2018, 106, 69-78.
  • Mandryk I.: Optymalizacja warunków hodowli zarodków uzyskanych po zapłodnieniu metodą ICSI świeżych i kriokonserwowanych oocytów świni. Doct. diss. Instytut Zootechniki, Balice 2013.
  • Nagai T., Yamauchi N., Kikuchi K.: Nuclear and cytoplasmic maturation in vitro of porcine oocytes. J. Reprod. Dev. 2001, 47, S55-S62.
  • Nakamura Y., Tajima S., Kikuchi K.: The quality after culture in vitro or in vivo of porcine oocytes matured and fertilized in vitro and their ability to develop to term. Anim. Sci. J. 2017, 88, 1916-1924.
  • Nguyen T. V., Tanihara F., Do L., Sato Y., Taniguchi M., Takagi M., Van Nguyen T., Otoi T.: Chlorogenic acid supplementation during in vitro maturation improves maturation, fertilization and developmental competence of porcine oocytes. Reprod. Domest. Anim. 2017, 52, 969-975.
  • Oberlender G., Murgas L. D. S., Zangeronimo M. G., Silva A. C., Menezes T. D. A., Pontelo T. P., Vieira L. A.: Role of insulin-like growth factor-I and follicular fluid from ovarian follicles with different diameters on porcine oocyte maturation and fertilization in vitro. Theriogenology 2013, 80, 4, 319-327.
  • Petters R. M.: In vitro culture of early stage embryos from livestock. Tiss. Cult. Res. Comm. 1992, 11, 305-313.
  • Petters R. M., Wells K. D.: Culture of pig embryos. J. Reprod. Fertil. 1993, 48, 61-73.
  • Poniedziałek-Kempny K.: Wpływ zmodyfikowanych warunków dojrzewania oocytów oraz jakości i sposobu przygotowania nasienia knura na pozaustrojowe zapłodnienie u świni. Doct. diss. Instytut Zootechniki, Balice 2019.
  • Romek M., Gajda B., Krzysztofowicz E., Kucia M., Uzarowska A., Smorąg Z.: Improved quality of porcine embryos cultured with hyaluronan due to the modification of the mitochondrial membrane potential and reactive oxygen species level. Theriogenology 2017, 102, 1-9.
  • Salhab M., Papillier P., Perreau Ch., Guyader-Joly C., Dupont J., Mermillod P., Uzbekova S.: Thymosins β-4 and β-10 are expressed in bovine ovarian follicles and upregulated in cumulus cells during meiotic maturation. Reprod. Fertil. Dev. 2010, 22, 1206-1221.
  • Sato E., Miyamoto H., Koide S.: Glycoaminoglycans in porcine follicular fluid promoting viability of oocytes in culture. Mol. Reprod. Dev. 1990, 26, 391-397.
  • Skowronek O., Zdebska N., Opiela J.: The impact of thymosin β4 on bovine oocytes meiotic maturation and fragmentation DNA. Proc. 4th Winter Workshop of the Society for Biology of Reproduction. Zakopane, 3-5 February 2016, p. 25.
  • Suzuki Ch., Iwamura Sh., Yoshioka K.: Birth of piglets through the non-surgical transfer of blastocysts produced in vitro. J. Reprod. Dev. 2004, 50, 487-491.
  • Yang J. G., Chen W. Y., Li P. S.: Effects of glucocorticoids on maturation of pig oocytes and their subsequent fertilizing capacity in vitro. Biol. Reprod. 1999, 70, 159-169.
  • Yoshida M., Mizoguchi Y., Ishigaki K., Kojima T., Nagai T.: Birth of piglets derived from in vitro fertilization of pig oocytes matured in vitro. Theriogenology 1993, 39, 1303-1311.
  • Yoshioka K.: Development and application of a chemically defined medium for the in vitro production of porcine embryos. J. Reprod. Dev. 2011, 57, 9-16.
  • Yoshioka K., Noguchi M., Suzuki Ch.: Production of piglets from in vitroproduced embryos following non-surgical transfer. Anim. Reprod. Sci. 2012, 131, 23-29.
  • Yoshioka K., Suzuki C., Itoh S., Kikuchi K., Iwamura S., Rodriquez-Martinez H.: Production of piglets derived from in vitro-produced blastocysts fertilized and cultured in chemically defined media: effects of theophylline, adenosine and cysteine during in vitro fertilization. Biol. Reprod. 2003, 69, 2092-2099.
  • Yoshioka K., Suzuki C., Tanaka A., Anas I., Iwamura S.: Birth of piglets derived from porcine zygotes cultured in a chemically defined medium. Biol. Reprod. 2002, 66, 112-119.
  • Yuan Y., Spate L. D., Redel B. K., Tian Y., Zhou J., Prather R. S.: Quadrupling efficiency in production of genetically modified pigs through improved oocyte maturation. PNAS 2017, E5796-E5804.
  • Zhang M. Z., Wang X., Yang H., Fogo A. B., Murphy B. J., Kaltenbach R., Cheng P., Zinker B., Harris R. C.: Lysophosphatidic Acid Receptor Antagonism Protects against Diabetic Nephropathy in a Type 2 Diabetic Model. J. Am. Soc. Nephrol. 2015, 28, 3300-3311.

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

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