Literature DB >> 11101038

Development and viability of pig oocytes matured in a protein-free medium containing epidermal growth factor.

L R Abeydeera1, W H Wang, T C Cantley, A Rieke, C N Murphy, R S Prather, B N Day.   

Abstract

This study examined the ability of epidermal growth factor (EGF) to improve the developmental competence of pig oocytes matured in a protein-free (PF) in vitro maturation (IVM) system. Oocyte maturation was done in one of three media: 1. PF-TCM: tissue culture medium (TCM) 199 + 0.1% polyvinylalcohol (PVA); 2. PF-TCM+EGF: PF-TCM + 10 ng/ml EGF; and 3. +ve CONT: North Carolina State University (NCSU) 23 medium + 10% porcine follicular fluid. All media contained 0.57 mM cysteine. Hormonal supplements, 0.5 microg/mL LH and 0.5 microg/mL FSH, were present only for the first half (20 to 22 h) of the culture period. After maturation, oocytes were co-incubated with frozen-thawed spermatozoa for 5 to 6 h and transferred to embryo culture medium, NCSU 23 containing 0.4% BSA, for 144 h. In Experiment 1, differences in cumulus expansion were observed for oocytes matured in +ve CONT (Category 4), PF-TCM (Category 2) and PF-TCM+EGF (Category 3). However, no significant differences in nuclear maturation to metaphase II stage were observed. In Experiment 2, no differences in fertilization parameters were observed. Significant (P < 0.01) differences in cleavage rates were observed among the three media for a proportion of the oocytes matured (52, 60 and 69% in PF-TCM, PF-TCM+EGF, and +ve CONT, respectively). Oocytes matured in PF-TCM showed the lowest (P < 0.01) blastocyst development (22%). However, the same rate of blastocyst development was obtained for +ve CONT (37%) and PF-TCM+EGF (37%). Blastocyst cell numbers were significantly higher when oocytes were matured in the presence of EGF (26 vs. 37 to 41). In Experiment 3, oocytes matured in PF-TCM+EGF had a significantly (P < 0.05) higher intracellular glutathione (GSH) concentration (5.9 vs. 11.4 pmol/oocyte) compared with PF-TCM. Twenty-two of 25 embryo transfer recipients became pregnant (Experiment 4). Four animals returned to estrus in within 60 days. Six pregnant animals slaughtered at 26 to 45 days had 43 fetuses (range: 4 to 12) and the remaining 12 animals farrowed 82 piglets (range: 3 to 12). These results indicate that EGF enhances the developmental competence of pig oocytes matured in a protein-free culture medium which is correlated with higher GSH level in oocytes. Birth of piglets indicate that embryos derived from oocytes matured in the presence of EGF are viable.

Entities:  

Mesh:

Substances:

Year:  2000        PMID: 11101038     DOI: 10.1016/S0093-691X(00)00390-3

Source DB:  PubMed          Journal:  Theriogenology        ISSN: 0093-691X            Impact factor:   2.740


  8 in total

1.  Regulation of oocyte mitochondrial DNA copy number by follicular fluid, EGF, and neuregulin 1 during in vitro maturation affects embryo development in pigs.

Authors:  J Mao; K M Whitworth; L D Spate; E M Walters; J Zhao; R S Prather
Journal:  Theriogenology       Date:  2012-05-22       Impact factor: 2.740

2.  Discovery of putative oocyte quality markers by comparative ExacTag proteomics.

Authors:  Michael D Powell; Gaurishankar Manandhar; Lee Spate; Miriam Sutovsky; Shawn Zimmerman; Shrikesh C Sachdev; Mark Hannink; Randall S Prather; Peter Sutovsky
Journal:  Proteomics Clin Appl       Date:  2010-01-04       Impact factor: 3.494

3.  Production of heterozygous alpha 1,3-galactosyltransferase (GGTA1) knock-out transgenic miniature pigs expressing human CD39.

Authors:  Kimyung Choi; Joohyun Shim; Nayoung Ko; Heejong Eom; Jiho Kim; Jeong-Woong Lee; Dong-Il Jin; Hyunil Kim
Journal:  Transgenic Res       Date:  2016-11-09       Impact factor: 2.788

4.  Lamins A and C are present in the nuclei of early porcine embryos, with lamin A being distributed in large intranuclear foci.

Authors:  Helen A Foster; Paula Stokes; Katherine Forsey; Henry J Leese; Joanna M Bridger
Journal:  Chromosome Res       Date:  2007-01-09       Impact factor: 5.239

5.  Development of porcine embryos reconstituted with somatic cells and enucleated metaphase I and II oocytes matured in a protein-free medium.

Authors:  K Miyoshi; S J Rzucidlo; J R Gibbons; S Arat; S L Stice
Journal:  BMC Dev Biol       Date:  2001-07-11       Impact factor: 1.978

6.  Successful non-surgical deep uterine transfer of porcine morulae after 24 hour culture in a chemically defined medium.

Authors:  Emilio A Martinez; Miguel Angel Angel; Cristina Cuello; Jonatan Sanchez-Osorio; Jesus Gomis; Inmaculada Parrilla; Jordi Vila; Ignaci Colina; Marta Diaz; Josep Reixach; Jose Luis Vazquez; Juan Maria Vazquez; Jordi Roca; Maria Antonia Gil
Journal:  PLoS One       Date:  2014-08-13       Impact factor: 3.240

7.  ФC31 Integrase-Mediated Isolation and Characterization of Novel Safe Harbors for Transgene Expression in the Pig Genome.

Authors:  Yanzhen Bi; Zaidong Hua; Hongyan Ren; Liping Zhang; Hongwei Xiao; Ximei Liu; Wenjun Hua; Shuqi Mei; Adrian Molenaar; Götz Laible; Xinmin Zheng
Journal:  Int J Mol Sci       Date:  2018-01-04       Impact factor: 5.923

8.  Systematic in vitro and in vivo characterization of Leukemia-inhibiting factor- and Fibroblast growth factor-derived porcine induced pluripotent stem cells.

Authors:  Jan O Secher; Ahmet Ceylan; Gianluca Mazzoni; Kaveh Mashayekhi; Tong Li; Suchitra Muenthaisong; Troels T Nielsen; Dong Li; Shengting Li; Stoyan Petkov; Susanna Cirera; Yonglun Luo; Lori Thombs; Haja N Kadarmideen; Andras Dinnyes; Lars Bolund; Bernard A J Roelen; Mette Schmidt; Henrik Callesen; Poul Hyttel; Kristine K Freude
Journal:  Mol Reprod Dev       Date:  2017-03       Impact factor: 2.609

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.