Literature DB >> 10734400

The ovine uterus as a host for in vitro-produced bovine embryos.

C E Rexroad1, A M Powell.   

Abstract

A series of experiments were conducted to determine whether bovine blastocysts would develop beyond the blastocyst stage in the ovine uterine environment. In Experiment 1, in vitro matured, fertilized and cultured (IVM/IVF/IVC) expanded bovine blastocysts were transferred into uteri of ewes on Day 7 or 9 of the estrous cycle and collected on Day 14 or 15 to determine if the bovine blastocysts would elongate and form an embryonic disk. Springtime trials with ewes that were synchronized with a medroxyprogesterone acetate (MAP) sponge resulted in a 78% blastocyst recovery rate, and 68% of the recovered spherical or elongated embryos had embryonic disks. In Experiment 2, transfer of 4-cell bovine embryos to the oviducts of ewes at Day 3 resulted in a lower recovery (47 vs 80%) than the transfer of blastocysts at Day 7 when embryos were recovered at Day 14. However, the percentage of embryos containing embryonic disks was higher for embryos transferred at the 4-cell stage (71%) than for embryos transferred as blastocysts (50%). In Experiment 3, IVF embryos from super-ovulated cows or Day 8 in vitro produced embryos transferred to cows were collected at Day 14 and were found to be similar in size to those produced by transfer to ewes in Experiment 2. In Experiment 4, the transfer of bovine blastocysts to ewes did not prolong the ovine estrous cycle. In Experiment 5, extension of the ovine estrous cycle by administration of a MAP releasing intravaginal device allowed bovine embryos to elongate extensively and to become filamentous. In Experiment 6, uterine flushings on Day 14 or Day 16 contained elevated levels of interferon-tau when bovine blastocyst were transferred on Day 7. Transfer of bovine embryos to the reproductive tract of a ewe allows some embryos to develop normally to advanced perimplantation stages and may be a useful tool for studying critical stages of embryo development and the developmental capacity of experimental embryos.

Entities:  

Mesh:

Year:  1999        PMID: 10734400     DOI: 10.1016/S0093-691X(99)00134-X

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


  4 in total

1.  Viral particles of endogenous betaretroviruses are released in the sheep uterus and infect the conceptus trophectoderm in a transspecies embryo transfer model.

Authors:  Sarah G Black; Frederick Arnaud; Robert C Burghardt; M Carey Satterfield; Jo-Ann G W Fleming; Charles R Long; Carol Hanna; Lita Murphy; Roman Biek; Massimo Palmarini; Thomas E Spencer
Journal:  J Virol       Date:  2010-07-07       Impact factor: 5.103

2.  Establishment of a bovine blastocyst-derived cell line collection for the comparative analysis of embryos created in vivo and by in vitro fertilization, somatic cell nuclear transfer, or parthenogenetic activation.

Authors:  Neil C Talbot; Anne M Powell; Mary Camp; Alan D Ealy
Journal:  In Vitro Cell Dev Biol Anim       Date:  2007-03-21       Impact factor: 2.416

3.  High developmental potential in vitro and in vivo of cattle embryos cloned without micromanipulators.

Authors:  Lleretny Rodríguez; Felipe I Navarrete; Heribelt Tovar; José F Cox; Fidel Ovidio Castro
Journal:  J Assist Reprod Genet       Date:  2008-01-18       Impact factor: 3.412

4.  Discovery and characterization of an epithelial-specific galectin in the endometrium that forms crystals in the trophectoderm.

Authors:  C Allison Gray; David L Adelson; Fuller W Bazer; Robert C Burghardt; Els N T Meeusen; Thomas E Spencer
Journal:  Proc Natl Acad Sci U S A       Date:  2004-05-17       Impact factor: 11.205

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.