Literature DB >> 16436529

Injection of somatic cell cytoplasm into oocytes before intracytoplasmic sperm injection impairs full-term development and increases placental weight in mice.

Nguyen Van Thuan1, Sayaka Wakayama, Satoshi Kishigami, Hiroshi Ohta, Takafusa Hikichi, Eiji Mizutani, Hong-Thuy Bui, Teruhiko Wakayama.   

Abstract

This study investigated the effects on fertilized embryo development of somatic cytoplasm after its injection into intact mouse oocytes. Mature oocytes collected from female B6D2F1 mice were injected with cumulus cell cytoplasm of different volumes and from different mouse strains (B6D2F1, ICR, and C57BL/6), or with embryonic cytoplasm. After culture for 1 h, B6D2F1 sperm were injected into those oocytes by intracytoplasmic sperm injection (ICSI). The oocytes were examined for pre- and postimplantation developmental competence. Increases in the volume of the somatic cytoplasm from onefold to fourfold resulted in an impairment of blastocyst development and full-term development (28% and 7%, respectively, vs. 96% and 63%, respectively, in the control group; P < 0.01). An increase in the volume of somatic cytoplasm reduced the expression of POU5F1 (more commonly known as OCT4) in expanded blastocysts. The frequency of embryos that developed to the blastocyst stage did not differ when B6D2F1 or ICR somatic cytoplasm was injected, but injection of C57BL/6 somatic cytoplasm induced a two-cell block in embryo development. Injection of the cytoplasm from fertilized embryos did not reduce the frequency of embryos attaining full-term development. Interestingly, somatic cytoplasm significantly increased the placental weight of ICSI embryos, even the injection of onefold cytoplasm (0.20 +/- 0.02 [n = 32] vs. 0.12 +/- 0.02 in the control group [n = 87]; P < 0.01). These findings indicate that the injection of somatic cytoplasm into oocytes before ICSI causes a decrease in preimplantation development, clearly impairs full-term development, and causes placental overgrowth in fertilized embryos. To our knowledge, placental overgrowth phenotypes are only caused by interspecies hybridization and cloning, and in genetically modified mice. Here, we report for the first time that somatic cytoplasm causes abnormal placentas in fertilized embryos. This study suggests that somatic cell cytoplasmic material is one cause of the low rate of full-term development in cloned mammals.

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Year:  2006        PMID: 16436529     DOI: 10.1095/biolreprod.105.047803

Source DB:  PubMed          Journal:  Biol Reprod        ISSN: 0006-3363            Impact factor:   4.285


  7 in total

1.  Transgenic chicken, mice, cattle, and pig embryos by somatic cell nuclear transfer into pig oocytes.

Authors:  Mukesh Kumar Gupta; Ziban Chandra Das; Young Tae Heo; Jin Young Joo; Hak-Jae Chung; Hyuk Song; Jae-Hwan Kim; Nam-Hyung Kim; Hoon Taek Lee; Dae Hwan Ko; Sang Jun Uhm
Journal:  Cell Reprogram       Date:  2013-06-28       Impact factor: 1.987

2.  Placental inflammation and oxidative stress in the mouse model of assisted reproduction.

Authors:  J M Raunig; Y Yamauchi; M A Ward; A C Collier
Journal:  Placenta       Date:  2011-09-01       Impact factor: 3.481

3.  Assisted reproduction technologies impair placental steroid metabolism.

Authors:  Abby C Collier; Shogo J Miyagi; Yasuhiro Yamauchi; Monika A Ward
Journal:  J Steroid Biochem Mol Biol       Date:  2009-05-03       Impact factor: 4.292

4.  Abnormal gene expression in regular and aggregated somatic cell nuclear transfer placentas.

Authors:  Bo-Woong Sim; Chae-Won Park; Myung-Hwa Kang; Kwan-Sik Min
Journal:  BMC Biotechnol       Date:  2017-03-27       Impact factor: 2.563

5.  Effects of pyruvate and dimethyl-α-ketoglutarate, either alone or in combination, on pre- and post-implantation development of mouse zygotes cultured in vitro.

Authors:  Eun Sol Choi; Koga Kawano; Misaki Hiraya; Eibai Matsukawa; Masayasu Yamada
Journal:  Reprod Med Biol       Date:  2019-07-19

6.  Alteration of fatty acid metabolism in the liver, adipose tissue, and testis of male mice conceived through assisted reproductive technologies: fatty acid metabolism in ART mice.

Authors:  Li-Ya Wang; Fang Le; Ning Wang; Lei Li; Xiao-Zhen Liu; Ying-Ming Zheng; Hang-Ying Lou; Xiang-Rong Xu; Yun-Long Chen; Xiao-Ming Zhu; He-Feng Huang; Fan Jin
Journal:  Lipids Health Dis       Date:  2013-01-23       Impact factor: 3.876

7.  Nuclear reprogramming of sperm and somatic nuclei in eggs and oocytes.

Authors:  Marta Teperek; Kei Miyamoto
Journal:  Reprod Med Biol       Date:  2013-06-04
  7 in total

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