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The blastocyst production rate and incidence of chromosomal abnormalities by developmental stage in in vitro produced porcine embryos.

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TLDR
Porcine in vitro production (IVP) yielded a high blastocyst rate and an excellent embryo quality when 3- to 4-cell and 5- to 8-cell stage embryos were selected on Day 2 after insemination and the same criteria yielded a higher quality of expanded blastocysts based on the stage of embryo development and morphology.
Abstract
The present study was conducted to determine the relationship between embryonic development speed at different stages (the cleaved stage at 52 h and the blastocyst stage at 6 days post insemination) and incidences of chromosome abnormalities in in vitro produced porcine embryos. Porcine oocytes were collected from 3-6-mm ovarian follicles obtained at a slaughterhouse and matured in modified NCSU-37 medium for 44-46 h. Following in vitro fertilization with a final concentration of 1 x 10(5) sperm/ml for 3 h, all oocytes were cultured in vitro for 52 h. Day-2 (52 h after insemination) embryos were classified according to their cleaved stages into 2-cell, 3- to 4-cell, 5- to 8-cell, and >8-cell stages; these were cultured separately for additional 4 days (Day 6). The resultant Day-6 blastocysts were classified according to the morphological diameter into 3 grades: Grade A, expanded blastocysts; Grade B, expanding blastocysts; and Grade C, early blastocysts. They were then analyzed chromosomally. The 3- to 4-cell and 5- to 8-cell embryos had significantly high blastocyst development rates (46.1 and 36.9%, respectively), and these blastocysts contained significantly more cells (40.2 and 42.4 cells, respectively) than those derived from 2-cell embryos and >8-cell embryos (28.6 and 26.5 cells, respectively). The incidence of chromosomal abnormalities was significantly higher in the blastocysts derived from 2-cell and >8-cell stage embryos than in the blastocysts derived from the other stage embryos. Furthermore, the grade A blastocysts had the lowest incidence of chromosomal abnormalities (35.3%) and contained the most cells (48.7 cells). Porcine in vitro production (IVP) yielded a high blastocyst rate and an excellent embryo quality when 3- to 4-cell and 5- to 8-cell stage embryos were selected on Day 2 after insemination. The same criteria yielded a higher quality of expanded blastocysts based on the stage of embryo development and morphology.

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Journal ArticleDOI

Factors affecting cryopreservation of porcine oocytes.

TL;DR: The aim of the present review is to summarize knowledge on viability and developmental competence of vitrified porcine oocytes and to give ideas for future perspectives for the improvement of porCine oocyte cryopreservation technology.
Journal ArticleDOI

Advances on in vitro production and cryopreservation of porcine embryos.

TL;DR: The presented methods and techniques make it possible to modify the characteristics of oocytes and embryos and thus may become major tools in mammalian gamete and embryo agricultural or biotechnological applications in the future.
Journal ArticleDOI

Culture of pig embryos

TL;DR: Adoption of a standard medium that could be used by different laboratories and, perhaps, with different species is suggested to simplify experimental protocols, enhance studies of comparative embryonic physiology and metabolism, and expedite transfer of information obtained in different species.
Journal ArticleDOI

Factors and methods of pig oocyte and embryo quality improvement and their application in reproductive biotechnology.

Barbara Gajda
- 01 Jul 2009 - 
TL;DR: The presented methods make it possible to modify the characteristics of oocytes and embryos and thus increase their susceptibility to cryopreservation and cloning.
References
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Journal Article

Culture of pig embryos

TL;DR: Pig embryos can be cultured using a number of different strategies including complex approaches like culture in vivo in a surrogate oviduct (rabbit, sheep, mouse), co-culture of embryos with cells in addition to simple approaches such as culture in defined media or salt solutions as mentioned in this paper.
Journal ArticleDOI

Production of cloned pigs from in vitro systems.

TL;DR: The cell culture and nuclear transfer techniques described here should allow the use of genetic modification procedures to produce tissues and organs from cloned pigs with reduced immunogenicity for use in xenotransplantation.
Journal ArticleDOI

Successful Piglet Production after Transfer of Blastocysts Produced by a Modified In Vitro System

TL;DR: The results suggest that an excellent piglet production system can be established by using this modified IVP system, which produces high-quality porcine blastocysts and has advantages for the generation of cloned and transgenic pigs.
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