Dae Hwan Ko's research while affiliated with Gyeongsang National University and other places

Publications (9)

Article
Full-text available
The purpose of this study is to develop transgenic cell line expressing targeted human granulocyte colony stimulating factor (hGCSF) and green fluorescence protein (GFP) genes as well as production of Somatic Cell Nuclear Transfer (SCNT) embryos derived from co-expressed transgenic donor cells. Constructed pPiggy-mWAP-hGCSF-EF1-GFP vector was chemi...
Article
Contents Assisted reproduction procedures, such as embryo transfer ( ET ) and artificial insemination ( AI ), in cattle could induce the secretion of prostaglandin F 2 ‐alpha ( PGF 2 α ) from uterine horns which may in turn interrupt embryo development and implantation. This study investigated the effect of flunixin meglumine ( FM ), prostaglandin...
Article
The purpose of this study is to improve production efficiency of vitrified-thawed transgenic bovine embryos. Transgenic bovine embryos were produced by injection of FIV-GFP lentiviral vector into perivitelline space of in vitro matured MⅡ stage oocytes, and then in vitro fertilization. EGFP-expressing transgenic bovine blastocysts were cultured in...
Article
Abstract This study explored the possibility of producing transgenic cloned embryos by interspecies somatic cell nuclear transfer (iSCNT) of cattle, mice, and chicken donor cells into enucleated pig oocytes. Enhanced green florescent protein (EGFP)-expressing donor cells were used for the nuclear transfer. Results showed that the occurrence of firs...
Article
The cryopreservation of sperm has contributed greatly to animal breeding and reproduction. This study was designed to examine the effect of raffinose, sucrose, and trehalose as cryoprotectants for freezing of mouse sperm. The cryoprotectant solution (CPA) consisting of 3% skim milk (Skim Milk dehydrated, Bacto, Difco, Seoul, Korea) as buffer or ext...
Article
Vitrification has been used to eliminate ice crystal formation during the cryopreservation of mammalian embryos. However, this method may introduce some problems such as loss of eggs during cryopreservation (EM grid) and damage to the zona pellucida. This study examined an alternative container (paper) for the vitrification of in vitro-produced bov...

Citations

... ET is an invasive procedure. And some studies have suggested that invasive intrauterine operations or the manipulation of the genital tract could induce the release of prostaglandins resulting in uterine contractions 31,33,34 . Then, the embryo was prevented from implanting in the uterine cavity. ...
... Pregnancy rates with this technique have exceeded 55% in large-scale trials (Hasler et al., 1995;Nibart and Humblot, 1997). However, for vitrification there are many variations in protocols (Ishimori et al., 1993;Park et al., 1999;Vajta et al., 1999;Kim et al., 2004;Vajta and Nagy, 2006). Vitrification of in vitro-derived embryos results in highly variable pregnancy rates after transfer; the reported range is 23-50% of transferred embryos, but most of studies involved small numbers of embryos (Kuwayama et al., 1992;Tachikawa et al., 1993;Agca et al., 1994;Wurth et al., 1994;Delval et al., 1996;Holm et al., 1996). ...
... The sperm samples were retrieved by flushing PBS through the vas deference, followed by the collection of sperm from the cauda epididymis, as described earlier (Sahoo et al. 2021). The motile spermatozoa were purified by the Swim-up in Sp-TALP media for 30 min (Gupta et al. 2013). The sperm pellet was collected by centrifugation at 800 g for 10 min. ...
... For prolific livestock species, the main handicap of vitrification is the low number of embryos that commercial devices can hold transmission [3,5,6]. Although attempts have been made to generate systems that allow cryopreservation of large numbers of embryos, such as hollow fiber [7] or the easily accessible paper container method [8], commercial, large holding capacity devices for minimum volume cooling vitrification of oocytes or embryos are non-existent. For rabbits, however, using the French straw device (without limitation on the number of embryos to be stored by device) provides an acceptable offspring production efficiency calculated as the ratio of the number of birth kits to the number of embryos transferred (ranging from 25% to 65%, [9]), while in pigs, when using the open pulled straw (OPS) method (from five to seven embryos by device) a lower offspring production efficiency has been reported (ranging from 7.1% to 23%, [9,10]. ...