Artificial control maturation of porcine oocyte by dibutyryl cyclicAMP

• Published in: Animal cells and systems Vol. 18; no. 1; pp. 52 - 58
• Main Authors: Zhao, Ming-Hui, Jin, Yong-Xun, Lee, Seul-Ki, Kim, Nam-Hyung, Cui, Xiang-Shun
• Format: Journal Article
• Language: English
• Published: England Taylor & Francis 01-02-2014; Taylor & Francis Ltd; 한국통합생물학회
• Subjects: Cytoskeleton; dbcAMP; maturation control; oocyte maturation; 생물학; dbcAMP; maturation control; oocyte maturation
• ISSN: 1976-8354; 2151-2485
• DOI: 10.1080/19768354.2014.880371

In this study, we investigated the effects of various durations of dibutyryl cyclic AMP (dbcAMP) treatment on the in vitro maturation (IVM) and subsequent development of parthenogenetically activated embryos. Immature porcine oocytes were cultured with or without 1 mM dbcAMP during the first 20, 28, or 36 h of culture, and then incubated for an additional 24 h without dbcAMP. The expression of Wee1B, Myt, and Cdc25B and the level of maturation promoting factor (MPF) in metaphase II oocytes were analyzed by real-time PCR (qRT-PCR) and enzyme linked immunosorbent assay (ELISA), respectively. The distribution of actin microfilaments in oocytes was also assessed. Subsequently, apoptotic cells in blastocysts from each group were visualized by transferase-mediated dUTP nick-end labeling staining. Results showed that oocytes extruded the first polar body between 12 and 18 h after being released from dbcAMP. MPF activity in oocytes at 28 + 24 h and 36 + 24 h after dbcAMP treatment was higher than that in the control group. Significantly more blastocysts were present among embryos in 28 + 24 h (54.28% vs. 39.11%, P < 0.05) and 36 + 24 h (47.24% vs. 32.94%, P < 0.05) groups than among embryos cultured in the absence of dbcAMP. However, the number of total and apoptotic cells was not significantly different between groups. The distribution of actin microfilaments was abnormal in oocytes cultured for 60 h without dbcAMP. In addition, the expression of Wee1B, Myt, and Cdc25B was higher in the control group at 44 h than in the dbcAMP group, but there were no differences in expression at the other time points. In conclusion, dbcAMP treatment delays oocyte maturation and maintains oocyte quality.