Effect of Epidermal Growth Factor (EGF) on Meiotic Maturation and Pronuclear Formation of Porcine Oocytes Produced In Vitro
* 본 문서는 배포용으로 복사 및 편집이 불가합니다.
서지정보
ㆍ발행기관 : 한국동물번식학회
ㆍ수록지정보 : Reproductive & developmental biology / 29권 / 2호
ㆍ저자명 : Song S. H., Kim J. G., Song H. J., Kumar B. Mohana, Cho S. R., Choe C. Y., Choi S. H., Rho G. J., Choe S. Y.
ㆍ저자명 : Song S. H., Kim J. G., Song H. J., Kumar B. Mohana, Cho S. R., Choe C. Y., Choi S. H., Rho G. J., Choe S. Y.
목차
INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES영어 초록
The objective of this study was to examine the effect of EGF on meiotic maturation and pronuclear (PN) formation of porcine oocytes. Prepubertal gilt cumulus-oocyte-complexes (COCs) aspirated from 2~6mm follicles of abbatoir ovaries were matured in TCM199 containing 0.1mg/ml cysteine, 0.5㎍/ml FSH and LH, and EGF (0, 5, 10, 20, 40 ng/ml) for 22 hr at 39℃ in a humidified atmosphere of 5% CO2 in air. They were then cultured for an additional 22hr without hormones. In Experiment 1, to examine the nuclear maturation at 44hr of culture, the expanded cumulus cells were removed by vortexing for 1 min in 3 mg/ml hyaluronidase. The oocytes were fixed in acetic acid: methanol (1:3, v/v) at least for 48 hr and stained with 1% orcein solution for 5 min. Nuclear status was classified as germinal vesicle (GV), germinal vesicle breakdown (GVBD), prophase-metaphase I (PI-MI), and PII-MII under microscope. In Experiment 2, to investigate PN formation, oocytes were fertilized with Percoll-treated freshly ejaculated sperm (1 x10 5 cells/ml) in mTBM with 0.3% BSA and 2mM caffeine for 5hr, and cultured in NCSU-23 medium with 0.4% BSA. At 6hr of culture, the embryos were fixed in 3.7% formaldehyde for 48hr and stained with 10ug/ml propidium iodide for 30 min. PN status was classified as no or one PN (unfertilized), 2 PN (normal fertilized) and ≥3 PN (polyspermy). Differences between groups were analyzed using one-way ANOVA after arc-sine transformation of the proportional data. The rate of oocytes that had reached to PII-MII were significantly (P<0.05) higher in all groups added EGF than that of non-treated group (67%), but it did not differ among the all added groups (86%, 85%, 79% and 81%, in 5, 10, 20 and 40 ng/ml EGF, respectively). No differences on the incidence of 2PN were observed in all treated groups (25%, 30%, 33%, 29% and 29%, in 0, 5, 10, 20 and 40 ng/ml EGF, respectively), however, in non-treated group, polyspermy tended to be increased (66% vs 58%, 54%, 52% and 55%, 0 vs. 5, 10, 20, 40 ng/ml EGF, respectively). These results suggest that EGF can be effectively used as an additive for enhancing oocyte maturation and reducing the incidence of polyspermy in pig.참고 자료
없음"Reproductive & developmental biology"의 다른 논문
Biological Activity of Recombinant Human Erythropoietin..5페이지
Cloned Placenta of Korean Native Calves Died Suddenly a..6페이지
Effects of Pyruvate and Taurine for In Vitro Preservati..7페이지
Effect of Inhibitor of Glycogen Synthase Kinase 3 on Se..7페이지
Production of Plasminogen Activators during In Vitro Ma..8페이지
Characterization of Placental Proteins in Bovine Somati..9페이지
Tumor Necrosis Factor-Related Apoptosis-Inducing Ligand..8페이지
Expression and Characterization of Purinergic Receptor,..7페이지
In Vitro Development of Mouse Parthenogenetic Embryos: ..4페이지
Effects of Estrus Status, Oocyte Diameter and Supplemen..5페이지