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http://dx.doi.org/10.12750/JET.2017.32.3.95

Optimization of Post-Activation Systems to Improve the Embryonic Development in Porcine Parthenogenesis and Somatic Cell Nuclear Transfer  

Roy, Pantu Kumar (College of Veterinary Medicine, Chungnam National University)
Kim, Ghangyong (College of Veterinary Medicine, Chungnam National University)
Fang, Xun (College of Veterinary Medicine, Chungnam National University)
Hassan, Bahia MS (College of Veterinary Medicine, Chungnam National University)
Soysa, Mahanama De (College of Veterinary Medicine, Chungnam National University)
Shin, Sang Tae (College of Veterinary Medicine, Chungnam National University)
Cho, Jong Ki (College of Veterinary Medicine, Chungnam National University)
Publication Information
Journal of Embryo Transfer / v.32, no.3, 2017 , pp. 95-104 More about this Journal
Abstract
This study was conducted to establish the optimal chemical post-activation conditions in porcine embryonic development after parthenogenesis (PA) and somatic cell nuclear transfer (SCNT) using 4 different chemical compositions (cytochalasin B (CB), cyclohexamide (CHX), demecolcine (DC), 6-dimethylaminopurine (DMAP). Porcine embryos were produced by PA and SCNT and then, cultured for post-activation with CB ($7.5{\mu}g/mL$), CB ($7.5{\mu}g/mL$) + CHX ($10{\mu}g/mL$), CB ($7.5{\mu}g/mL$) +DC ($0.4{\mu}g/mL$), and CB ($7.5{\mu}g/mL$) + DMAP (2 mM). In PA embryonic development, cleavage rates have been significantly higher in CB group (94.7%) and CB+DMAP group (94.1%) than that of CB+CHX and CB+DC group (88.1 and 84.3%, respectively). There have been no significant differences in blastocyst formation rates among the four groups. In cell number of blastocyst was shown in CB group (42.3%) significantly higher than CB+CHX and CB+DC group (40.6 and 40.6%, respectively). In SCNT embryonic development, CB+DMAP group (89.7%) significant differences were found on embryo cleavage rates when compared with other three groups. Blastocyst formation rates in CB+DMAP group (26.9%) were significantly higher when compared with CB, CB+CHX, and CB+DC groups (25.5, 20.2, and 22.1%, respectively). In blastocyst cell number, CB+DMAP group (41.4%) was found higher significant difference compared with other three groups. Additionally, we have investigated survivin expression in early development stages of porcine SCNT embryos for more confirmation. Our results establish that CB group and CB+DMAP group for 4 h during post-activation improves pre-implantation improvement of PA and SCNT embryos.
Keywords
Embryo; Cloning; Parthenogenesis; Pig; Post-activation;
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1 Himaki T, Mori H, Mizobe Y, Miyoshi K, Sato M, Takao S and Yoshida M. 2010. Latrunculin A Dramatically Improves the Developmental Capacity of Nuclear Transfer Embryos Derived from Gene-Modified Clawn Miniature Pig Cells. Cell Reprogram 12:127-131.   DOI
2 Holm IE, Alstrup AK and Luo Y. 2016. Genetically modified pig models for neurodegenerative disorders. J. Pathol. 238:267-287.   DOI
3 Ibanez E, Albertini DF and Overstrom EW. 2003. Demecolcine-induced oocyte enucleation for somatic cell cloning: coordination between cell-cycle egress, kinetics of cortical cytoskeletal interactions, and second polar body extrusion. Biol. Reprod. 68:1249-1258.   DOI
4 Im GS, Samuel M, Lai L, Hao Y and Prather RS. 2007. Development and calcium level changes in pre-implantation porcine nuclear transfer embryos activated with 6-DMAP after fusion. Mol. Reprod. Dev. 74:1158-1164.   DOI
5 Ito T, Sendai Y, Yamazaki S, Seki-Soma M, Hirose K, Watanabe M, Fukawa K and Nakauchi H. 2014. Generation of recombination activating gene-1-deficient neonatal piglets: a model of T and B cell deficient severe combined immune deficiency. PLoS One 9:e113833.   DOI
6 Jeon K, Kim EY, Tae JC, Lee CH, Lee KS, Kim YO, Jeong DK, Cho SK, Kim JH, Lee HY, Riu KZ, Cho SG and Park SP. 2008. Survivin protein expression in bovine follicular oocytes and their in vitro developmental competence. Anim. Reprod. Sci. 108:319-333.   DOI
7 Kawamura K, Sato N, Fukuda J, Kodama H, Kumagai J, Tanikawa H, Nakamura A, Honda Y, Sato T and Tanaka T. 2003. Ghrelin inhibits the development of mouse preimplantation embryos in vitro. Endocrinology 144:2623-2633.   DOI
8 Lee J, You J, Kim J, Hyun SH and Lee E. 2010. Postactivation treatment with nocodazole maintains normal nuclear ploidy of cloned pig embryos by increasing nuclear retention and formation of single pronucleus. Theriogenology 73:429-436.   DOI
9 Kim NH, Simerly C, Funahashi H, Schatten G and Day BN. 1996. Microtubule organization in porcine oocytes during fertilization and parthenogenesis. Biol. Reprod. 54:1397-1404.   DOI
10 Kurome M, Fujimura T, Murakami H, Takahagi Y, Wako N, Ochiai T, Miyazaki K and Nagashima H. 2003. Comparison of electro-fusion and intracytoplasmic nuclear injection methods in pig cloning. Cloning Stem Cells 5:367-378.   DOI
11 Lee JW, Tian XC and Yang X. 2004a. Optimization of parthenogenetic activation protocol in porcine. Mol. Reprod. Dev. 68:51-57.   DOI
12 Meena CR and Das SK. 2006. Development of water buffalo (Bubalus bubalis) embryos from in vitro matured oocytes reconstructed with fetal skin fibroblast cells as donor nuclei. Anim. Reprod. Sci. 93:258-267.   DOI
13 Miyazaki K, Tomii R, Kurome M, Ueda H, Hirakawa K, Ueno S, Hiruma K and Nagashima H. 2005. Evaluation of the quality of porcine somatic cell nuclear transfer embryo by gene transcription profiles. J. Reprod. Dev. 51:123-131.   DOI
14 Polejaeva IA, Chen SH, Vaught TD, Page RL, Mullins J, Ball S, Dai YF, Boone J, Walker S, Ayares DL, Colman A and Campbell KHS. 2000. Cloned pigs produced by nuclear transfer from adult somatic cells. Nature 407:86-90.   DOI
15 Miyoshi K, Yuki Y and Yoshida M. 2005. Optimization of Ca2+ concentrations in fusion and activation media for production of cloned embryos from miniature pig somatic cells. J. Reprod. Dev. 51:699-706.   DOI
16 Wilmut I, Schnieke AE, McWhir J, Kind AJ and Campbell KH. 1997. Viable offspring derived from fetal and adult mammalian cells. Nature 385:810-813.   DOI
17 Yi YJ and Park CS. 2005a. Parthenogenetic development of porcine oocytes treated by ethanol, cycloheximide, cytochalasin B and 6-dimethylaminopurine. Anim. Reprod. Sci. 86:297-304.   DOI
18 Yi YJ and Park CS. 2005b. Parthenogenetic development of porcine oocytes treated by ethanol, cycloheximide, cytochalasin B and 6-dimethylaminopurine. Anim. Reprod. Sci. 86:297-304.   DOI
19 Motlik J, Pavlok A, Kubelka M, Kalous J and Kalab P. 1998. Interplay between CDC2 kinase and MAP kinase pathway during maturation of mammalian oocytes. Theriogenology 49:461-469.   DOI
20 Park SY, Kim EY, Jeon K, Cui XS, Lee WD, Kim NH, Park SP and Lim JH. 2007. Survivin acts as anti-apoptotic factor during the development of bovine pre-implantation embryos. Mol. Reprod. Dev. 74:582-590.   DOI
21 Rieder CL and Palazzo RE. 1992. Colcemid and the mitotic cycle. J. Cell. Sci. 102(Pt 3):387-392.
22 Ruchaud S, Carmena M and Earnshaw WC. 2007. Chromosomal passengers: conducting cell division. Nat. Rev. Mol. Cell. Bio. 8:798-812.   DOI
23 Schneider-Poetsch T, Ju J, Eyler DE, Dang Y, Bhat S, Merrick WC, Green R, Shen B and Liu JO. 2010. Inhibition of eukaryotic translation elongation by cycloheximide and lactimidomycin. Nat. Chem. Biol. 6:209-217.   DOI
24 Song K, Hyun SH, Shin T and Lee E. 2009a. Post-activation treatment with demecolcine improves development of somatic cell nuclear transfer embryos in pigs by modifying the remodeling of donor nuclei. Mol. Reprod. Dev. 76:611-619.   DOI
25 Song K, Hyun SH, Shin T and Lee E. 2009b. Post-Activation Treatment With Demecolcine Improves Development of Somatic Cell Nuclear Transfer Embryos in Pigs by Modifying the Remodeling of Donor Nuclei. Mol. Reprod. Dev. 76:611-619.   DOI
26 Vichera G, Alfonso J, Duque CC, Silvestre MA, Pereyra-Bonnet F, Fernandez-Martin R and Salamone D. 2010. Chemical activation with a combination of ionomycin and dehydroleucodine for production of parthenogenetic, ICSI and cloned bovine embryos. Reprod. Domest. Anim. 45:e306-312.   DOI
27 Song K, Hyun SH, Shin T and Lee E. 2009c. Post-activation treatment with demecolcine improves development of somatic cell nuclear transfer embryos in pigs by modifying the remodeling of donor nuclei. Mol. Reprod. Dev. 76:611-619.   DOI
28 Szollosi MS, Kubiak JZ, Debey P, de Pennart H, Szollosi D and Maro B. 1993. Inhibition of protein kinases by 6-dimethylaminopurine accelerates the transition to interphase in activated mouse oocytes. J. Cell. Sci. 104(Pt 3):861-872.
29 Umeyama K, Honda K, Matsunari H, Nakano K, Hidaka T, Sekiguchi K, Mochizuki H, Takeuchi Y, Fujiwara T, Watanabe M, Nagaya M and Nagashima H. 2013. Production of diabetic offspring using cryopreserved epididymal sperm by in vitro fertilization and intrafallopian insemination techniques in transgenic pigs. J. Reprod. Dev. 59:599-603.   DOI
30 Zhu ZY, Chen DY, Li JS, Lian L, Lei L, Han Z.M and Sun QY. 2003. Rotation of meiotic spindle is controlled by microfilaments in mouse oocytes. Biol. Reprod. 68:943-946.   DOI
31 Bavister BD, Leibfried ML and Lieberman G. 1983. Development of preimplantation embryos of the golden hamster in a defined culture medium. Biol. Reprod. 28:235-247.   DOI
32 Betthauser J, Forsberg E, Augenstein M, Childs L, Eilertsen K, Enos J, Forsythe T, Golueke P, Jurgella G, Koppang R, Lesmeister T, Mallon K, Mell G, Misica P, Pace M, Pfister-Genskow M, Strelchenko N, Voelker G, Watt S, Thompson S and Bishop M. 2000a. Production of cloned pigs from in vitro systems. Nat. Biotechnol. 18:1055-1059.   DOI
33 Adida C, Crotty PL, McGrath J, Berrebi D, Diebold J and Altieri DC. 1998. Developmentally regulated expression of the novel cancer anti-apoptosis gene survivin in human and mouse differentiation. Ame. J. Patho. 152:43-49.
34 Cooper JA. 1987. Effects of cytochalasin and phalloidin on actin. J. Cell. Biol. 105:1473-1478.   DOI
35 Whitelaw CB, Sheets TP, Lillico SG and Telugu BP. 2016. Engineering large animal models of human disease. J. Pathol. 238:247-256.   DOI
36 Altieri DC. 2004. Molecular circuits of apoptosis regulation and cell division control: The survivin paradigm. J. Cell. Bioche. 92:656-663.   DOI
37 Betthauser J, Forsberg E, Augenstein M, Childs L, Eilertsen K, Enos J, Forsythe T, Golueke P, Jurgella G, Koppang R, Lesmeister T, Mallon K, Mell G, Misica P, Pace M, Pfister-Genskow M, Strelchenko N, Voelker G, Watt S, Thompson S and Bishop M. 2000b. Production of cloned pigs from in vitro systems. Nat. Biotechnol. 18:1055-1059.   DOI
38 Cervera RP, Silvestre MA, Marti N, Garcia-Mengual E, Moreno R and Stojkovic M. 2010. Effects of different oocyte activation procedures on development and gene expression of porcine pre-implantation embryos. Reprod. Domest. Anim. 45:e12-20.
39 Cheng WM, Sun XL, An L, Zhu SE, Li XH, Li Y and Tian JH. 2007. Effect of different parthenogenetic activation methods on the developmental competence of in vitro matured porcine oocytes. Anim. Biotechnol. 18:131-141.   DOI
40 Chieppa MN, Perota A, Corona C, Grindatto A, Lagutina I, Vallino Costassa E, Lazzari G, Colleoni S, Duchi R, Lucchini F, Caramelli M, Bendotti C, Galli C and Casalone C. 2014. Modeling amyotrophic lateral sclerosis in hSOD1 transgenic swine. Neu. Dis. 13:246-254.
41 De Sousa PA, Dobrinsky JR, Zhu J, Archibald AL, Ainslie A, Bosma W, Bowering J, Bracken J, Ferrier PM, Fletcher J, Gasparrini B, Harkness L, Johnston P, Ritchie M, Ritchie WA, Travers A, Albertini D, Dinnyes A, King TJ and Wilmut I. 2002. Somatic cell nuclear transfer in the pig: control of pronuclear formation and integration with improved methods for activation and maintenance of pregnancy. Biol. Reprod. 66:642-650.   DOI
42 Guo Q, Zhu HY, Jin L, Gao QS, Kang JD, Cui CD and Yin XJ. 2015. Production of Cloned Wuzhishan Miniature Pigs and Application for Alloxan Toxicity Test. Anim. Biotechnol. 26:292-297.   DOI
43 Du Y, Pribenszky CS, Molnar M, Zhang X, Yang H, Kuwayama M, Pedersen AM, Villemoes K, Bolund L and Vajta G. 2008. High hydrostatic pressure: a new way to improve in vitro developmental competence of porcine matured oocytes after vitrification. Reproduction 135:13-17.   DOI
44 Grupen CG, Mau JC, McIlfatrick SM, Maddocks S and Nottle MB. 2002. Effect of 6-dimethylaminopurine on electrically activated in vitro matured porcine oocytes. Mol. Reprod. Dev. 62:387-396.   DOI