Similar time restriction for intracytoplasmic sperm injection and round spermatid injection into activated oocytes for efficient offspring production

被引:49
作者
Kishigami, S [1 ]
Wakayama, S [1 ]
Van Thuan, N [1 ]
Wakayama, T [1 ]
机构
[1] RIKEN, Ctr Dev Biol, Lab Genome Reprogramming, Chuo Ku, Kobe, Hyogo 6500047, Japan
关键词
assisted reproductive technology; early development; gamete biology; sperm; spermatid;
D O I
10.1095/biolreprod.103.025171
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The injection of male haploid germ cells, such as spermatozoa and round spermatids, into preactivated mouse oocytes can result in the development of viable embryos and offspring. However, it is not clear how the timing of intracytoplasmic sperm injection (ICSI) and round spermatid injection (ROSI) affects the production of offspring. We carried out ICSI and ROSI every 20 min for up to 4 h after the activation of mouse oocytes by Sr2+ and compared the late-stage development of ICSI- and ROSI-treated oocytes, including the formation of pronuclei, blastocyst formation, and offspring production. The rate of pronucleus formation (RPF) after carrying out ICSI started to decrease from >95% at 100 min following oocyte activation and declined to <20% by 180 min. In comparison, RPF by ROSI decreased gradually from >70% between 0 and 4 h after activation. The RPFs were closely correlated with blastocyst formation. Offspring production for both ICSI and ROSI decreased significantly when injections were conducted after 100 min, a time at which activated oocytes were in the early G1 stage of the cell cycle. These results suggest that spermatozoa and round spermatids have different potentials for inducing the formation of a male pronucleus in activated oocytes, but ICSI and ROSI are both subject to the same time constraint for the efficient production of offspring, which is determined by the cell cycle of the activated oocyte.
引用
收藏
页码:1863 / 1869
页数:7
相关论文
共 31 条
[1]   CALCIUM OSCILLATIONS AND PROTEIN-SYNTHESIS INHIBITION SYNERGISTICALLY ACTIVATE MOUSE OOCYTES [J].
BOSMIKICH, A ;
SWANN, K ;
WHITTINGHAM, DG .
MOLECULAR REPRODUCTION AND DEVELOPMENT, 1995, 41 (01) :84-90
[2]  
CHATOT CL, 1989, J REPROD FERTIL, V86, P679, DOI 10.1530/jrf.0.0860679
[3]   Rescue of infertile transgenic rat lines by intracytoplasmic injection of cryopreserved round spermatids [J].
Hirabayashi, M ;
Kato, M ;
Aoto, T ;
Ueda, M ;
Hochi, S .
MOLECULAR REPRODUCTION AND DEVELOPMENT, 2002, 62 (03) :295-299
[4]   Restoration of spermatogenesis by lentiviral gene transfer: Offspring from infertile mice [J].
Ikawa, M ;
Tergaonkar, V ;
Ogura, A ;
Ogonuki, N ;
Inoue, K ;
Verma, IM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (11) :7524-7529
[5]   Allogeneic offspring produced by male germ line stem cell transplantation into infertile mouse testis [J].
Kanatsu-Shinohara, M ;
Ogonuki, N ;
Inoue, K ;
Ogura, A ;
Toyokuni, S ;
Honjo, T ;
Shinohara, T .
BIOLOGY OF REPRODUCTION, 2003, 68 (01) :167-173
[6]   Long-term proliferation in culture and germline transmission of mouse male germline stem cells [J].
Kanatsu-Shinohara, M ;
Ogonuki, N ;
Inoue, K ;
Miki, H ;
Ogura, A ;
Toyokuni, S ;
Shinohara, T .
BIOLOGY OF REPRODUCTION, 2003, 69 (02) :612-616
[7]   Adenovirus-mediated gene delivery and in vitro microinsemination produce offspring from infertile male mice [J].
Kanatsu-Shinohara, M ;
Ogura, A ;
Ikegawa, M ;
Inoue, K ;
Ogonuki, N ;
Tashiro, K ;
Toyokuni, S ;
Honjo, T ;
Shinohara, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (03) :1383-1388
[8]   Regulation of spermatogenesis by testis-specific, cytoplasmic poly(A) polymerase TPAP [J].
Kashiwabara, S ;
Noguchi, J ;
Zhuang, T ;
Ohmura, K ;
Honda, A ;
Sugiura, S ;
Miyamoto, K ;
Takahashi, S ;
Inoue, K ;
Ogura, A ;
Baba, T .
SCIENCE, 2002, 298 (5600) :1999-2002
[9]  
KIMURA Y, 1995, DEVELOPMENT, V121, P2397
[10]   INTRACYTOPLASMIC SPERM INJECTION IN THE MOUSE [J].
KIMURA, Y ;
YANAGIMACHI, R .
BIOLOGY OF REPRODUCTION, 1995, 52 (04) :709-720