Back to Search
Start Over
Production and Breeding of Transgenic Cloned Pigs Expressing Human CD73.
- Source :
-
Development & reproduction [Dev Reprod] 2017 Jun; Vol. 21 (2), pp. 157-165. Date of Electronic Publication: 2017 Jun 30. - Publication Year :
- 2017
-
Abstract
- One of the reasons to causing blood coagulation in the tissue of xenografted organs was known to incompatibility of the blood coagulation and anti-coagulation regulatory system between TG pigs and primates. Thus, overexpression of human CD73 (hCD73) in the pig endothelial cells is considered as a method to reduce coagulopathy after pig-to-non-human-primate xenotransplantation. This study was performed to produce and breed transgenic pigs expressing hCD73 for the studies immune rejection responses and could provide a successful application of xenotransplantation. The transgenic cells were constructed an hCD73 expression vector under control porcine Icam2 promoter (pIcam2-hCD73) and established donor cell lines expressing hCD73. The numbers of transferred reconstructed embryos were 127 ± 18.9. The pregnancy and delivery rate of surrogates were 8/18 (44%) and 3/18 (16%). The total number of delivered cloned pigs were 10 (2 alive, 7 mummy, and 1 died after birth). Among them, three live hCD73-pigs were successfully delivered by Caesarean section, but one was dead after birth. The two hCD73 TG cloned pigs had normal reproductive ability. They mated with wild type (WT) MGH (Massachusetts General Hospital) female sows and produced totally 16 piglets. Among them, 5 piglets were identified as hCD73 TG pigs. In conclusion, we successfully generated the hCD73 transgenic cloned pigs and produced their litters by natural mating. It can be possible to use a mate for the production of multiple transgenic pigs such as α-1,3-galactosyltransferase knock-out /hCD46 for xenotransplantation.
Details
- Language :
- English
- ISSN :
- 2465-9525
- Volume :
- 21
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Development & reproduction
- Publication Type :
- Academic Journal
- Accession number :
- 28785737
- Full Text :
- https://doi.org/10.12717/DR.2017.21.2.157