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Low levels of chimerism in rabbit fetuses produced from preimplantation embryos microinjected with fetal gonadal cells.

作者信息

Moens A, Betteridge K J, Brunet A, Renard J P

机构信息

Unité de Biologie du Développement, INRA, Jouy-en-Josas, France.

出版信息

Mol Reprod Dev. 1996 Jan;43(1):38-46. doi: 10.1002/(SICI)1098-2795(199601)43:1<38::AID-MRD5>3.0.CO;2-V.

DOI:10.1002/(SICI)1098-2795(199601)43:1<38::AID-MRD5>3.0.CO;2-V
PMID:8720111
Abstract

The potential pluripotency of rabbit fetal germ cells has been investigated by using them to make chimeric embryos. Gonial cells, isolated from enzyme-dispersed male and female transgenic fetal rabbit gonads of 18-22 days gestation, were microinjected in groups of about 10 into 640 nontransgenic rabbit embryos between the two-cell and expanded blastocyst stages. Injections were made with primary isolations of gonial cells, within 48 hr of their collection. The injected embryos were transferred, with or without non-injected control embryos, into 49 recipient rabbits. Tissues from 159 resulting fetuses, implantation sites, and a few liveborn young were examined by PCR analysis for the two transgenes used (alpha-1 antitrypsin or luciferase). The overall pregnancy rate (about 80%) was not affected by the stage of development of the embryo injected, nor by co-transfer of control embryos. The survival rate of injected embryos (18% overall, 23.6% in pregnant recipients) was almost identical to that of 243 control embryos. Chimerism was detectable in tissues produced from 4 of 159 (2.5%) of the injected embryos, all four of which had been injected at the 8- to 16-cell stage. This low rate of success indicates that, although passage of rabbit gonial cells is not an absolute requirement for pluripotency, further investigation should pay particular attention to improving culture conditions with a view to deriving EG cell lines.

摘要

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