Improving the Quality of Miniature Pig Somatic Cell Nuclear Transfer Blastocysts: Aggregation of SCNT Embryos at the Four-cell Stage

被引:23
作者
Terashita, Y. [1 ]
Sugimura, S. [1 ]
Kudo, Y. [1 ]
Amano, R. [1 ]
Hiradate, Y. [1 ]
Sato, E. [1 ]
机构
[1] Tohoku Univ, Lab Anim Reprod, Grad Sch Agr Sci, Aoba Ku, Sendai, Miyagi 9818555, Japan
基金
日本学术振兴会;
关键词
GAP JUNCTIONAL COMMUNICATION; IN-VITRO DEVELOPMENT; MOUSE EMBRYOS; CO-TRANSFER; CLONING; EXPRESSION; OOCYTES; SYSTEM; PLURIPOTENCY; COMPETENCE;
D O I
10.1111/j.1439-0531.2010.01614.x
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
Contents Miniature pigs share many similar characteristics such as anatomy, physiology and body size with humans and are expected to become important animal models for therapeutic cloning using embryonic stem cells (ESCs) derived by somatic cell nuclear transfer (SCNT). In the present study, we observed that miniature pig SCNT blastocysts possessed a lower total number of nuclei and a lower percentage of POU5F1-positive cells than those possessed by in vitro fertilized (IVF) blastocysts. To overcome these problems, we evaluated the applicability of aggregating miniature pig SCNT embryos at the four-cell stage. We showed that (i) aggregation of two or three miniature pig SCNT embryos at the four-cell stage improves the total number of nuclei and the percentage of POU5F1-positive cells in blastocysts, and (ii) IVF blastocysts with low cell numbers induced by the removal of two blastomeres at the four-cell stage did not exhibit a decrease in the percentage of POU5F1-positive cells. These results suggest that the aggregation of miniature pig SCNT embryos at the four-cell stage can be a useful technique for improving the quality of miniature pig SCNT blastocysts and indicating that improvement in the percentage of POU5F1-positive cells in aggregated SCNT embryos is not simply the consequence of increased cell numbers.
引用
收藏
页码:189 / 196
页数:8
相关论文
共 43 条
[1]   Culture of preimplantation embryos: Facts and artifacts [J].
Bavister, BD .
HUMAN REPRODUCTION UPDATE, 1995, 1 (02) :91-148
[2]   Pluripotency deficit in clones overcome by clone-clone aggregation:: epigenetic complementation? [J].
Boiani, M ;
Eckardt, S ;
Leu, NA ;
Schöler, HR ;
McLaughlin, KJ .
EMBO JOURNAL, 2003, 22 (19) :5304-5312
[3]   Oct4 distribution and level in mouse clones:: consequences for pluripotency [J].
Boiani, M ;
Eckardt, S ;
Schöler, HR ;
McLaughlin, KJ .
GENES & DEVELOPMENT, 2002, 16 (10) :1209-1219
[4]   Incomplete reactivation of Oct4-related genes in mouse embryos cloned from somatic nuclei [J].
Bortvin, A ;
Eggan, K ;
Skaletsky, H ;
Akutsu, H ;
Berry, DL ;
Yanagimachi, R ;
Page, DC ;
Jaenisch, R .
DEVELOPMENT, 2003, 130 (08) :1673-1680
[5]  
BRONSON RA, 1970, J REPROD FERTIL, V22, P129, DOI 10.1530/jrf.0.0220129
[6]   Induction of Oct-3/4 expression in somatic cells by gap junction-mediated cAMP signaling from blastomeres [J].
Burnside, AS ;
Collas, P .
EUROPEAN JOURNAL OF CELL BIOLOGY, 2002, 81 (11) :585-591
[7]   Targeted disruption of the α1,3-galactosyltransferase gene in cloned pigs [J].
Dai, YF ;
Vaught, TD ;
Boone, J ;
Chen, SH ;
Phelps, CJ ;
Ball, S ;
Monahan, JA ;
Jobst, PM ;
McCreath, KJ ;
Lamborn, AE ;
Cowell-Lucero, JL ;
Wells, KD ;
Colman, A ;
Polejaeva, IA ;
Ayares, DL .
NATURE BIOTECHNOLOGY, 2002, 20 (03) :251-255
[8]   Interpretation of reprogramming to predict the success of somatic cell cloning [J].
Eckardt, S ;
McLaughlin, KJ .
ANIMAL REPRODUCTION SCIENCE, 2004, 82-3 :97-108
[9]   Successful cloning of the Yucatan minipig using commercial/occidental breeds as oocyte donors and embryo recipients [J].
Estrada, Jose L. ;
Collins, Bruce ;
York, Abby ;
Bischoff, Steve ;
Sommer, Jeff ;
Tsai, Shengdar ;
Petters, Robert M. ;
Piedrahita, Jorge A. .
CLONING AND STEM CELLS, 2008, 10 (02) :287-296
[10]   Culture and selection of viable blastocysts: a feasible proposition for human IVF? [J].
Gardner, DK ;
Lane, M .
HUMAN REPRODUCTION UPDATE, 1997, 3 (04) :367-382