A paucity of structural integrity in cloned porcine blastocysts produced in vitro

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Title
A paucity of structural integrity in cloned porcine blastocysts produced in vitro
Author(s)
Deog Bon Koo; Yong-Kook KangJung Sun Park; J K Park; W K Chang; Kyung Kwang Lee; Yong Mahn Han
Bibliographic Citation
Theriogenology, vol. 62, no. 5, pp. 779-789
Publication Year
2004
Abstract
The structural integrity of blastocyst stage embryos, consisting of the inner cell mass (ICM) and trophectoderm (TE) cells, is a prerequisite for normal development after implantation in mammals. In this study, allocation of nuclear transfer (NT)-derived porcine blastocysts to the ICM and to the TE cells was examined and compared with IVF- and in vivo-derived embryos. NT-derived embryos had a lower developmental competence to the blastocyst stage than IVF-derived embryos (P<0.05). Total cell number of NT-derived blastocysts was inferior to that of IVF-derived embryos (P<0.05), although no difference was detected between the two groups in the ratio of ICM to total cells. However, in vivo-derived blastocysts had a higher proportion of ICM to total cells compared with in vitro-produced embryos (P<0.01). To investigate what proportions of in vitro-produced porcine embryos represent normal structural integrity, differentially-stained blastocysts were individually classified into three presumptive groups (I: <20%; II: 20-40%; III: >40%) according to the ratio of ICM to total cells. Low proportions of NT- (12.5%, 7/56) and IVF-derived blastocysts (15.8%, 9/57) were assigned to Group II, presumptively having a normal range of structural integrity, whereas, almost all in vivo-derived embryos (97.5%, 39/40) were allocated to Group II. In conclusion, limited structural integrity may lead to the poor survival to term of NT- or IVF-derived porcine embryos produced in vitro.
Keyword
BlastocystDifferential stainingIn vitro fertilizationNuclear transferPorcine
ISSN
0093-691X
Publisher
Elsevier
DOI
http://dx.doi.org/10.1016/j.theriogenology.2003.12.027
Type
Article
Appears in Collections:
Aging Convergence Research Center > 1. Journal Articles
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