Chimeric pigs following blastocyst injection of transgenic porcine primordial germ cells

• Published in: Molecular reproduction and development 1999-11, Vol.54 (3), p.244-254
• Main Authors: Mueller, S, Prelle, K, Rieger, N, Petznek, H, Lassnig, C, Luksch, U, Aigner, B, Baetscher, M, Wolf, E, Mueller, M
• Format: Article
• Language: English
• Subjects: Animals; Animals, Genetically Modified; Biological and medical sciences; Biotechnology; blastocyst; Blastocyst - metabolism; cell lines; Cells, Cultured; chimera; chimerism; Cryopreservation; Female; fetus; Fundamental and applied biological sciences. Psychology; Genetic engineering; Genetic technics; Germ Cells; immunocytochemistry; Karyotyping; Lewis X Antigen - metabolism; Male; Methods. Procedures. Technologies; pig; piglets; pluripotency; primordial germ cells; Swine; Tissue Transplantation - methods; Transgenic animals; Transgenic animals and transgenic plants; Transplantation Chimera - genetics
• ISSN: 1040-452X; 1098-2795
• DOI: 10.1002/(SICI)1098-2795(199911)54:3<244::AID-MRD5>3.0.CO;2-5

Porcine primordial germ cell (PGC) derived cell lines of WAPhGH‐transgenic pigs have been established that were able to contribute to chimeras. PGCs were isolated from day 25 to 28 genital ridges of more than 30 individual transgenic fetuses in order to have an easy to follow marker gene. To support undifferentiated growth, cell lines were derived and stable maintained on STO no. 8 feeder cells, a murine embryonic fibroblast cell line expressing recombinant, membrane‐bound porcine stem cell factor (SCF). Fifteen lines proliferated in an undifferentiated state up to passage 13; two lines were maintained for more than 23 passages. Cell staining experiments for differentiation markers in several cell lines, indicated the presence of pluripotent cells in prolonged cultures. Further characterization using karyotyping revealed a normal, euploid set of chromosomes in cells of passages 15 and higher. Pluripotency of freshly isolated, short‐term (up to 24 hr before injection) and long‐term cultured, frozen/thawed cells was tested by injection into day 6 recipient blastocysts to give rise to chimeric piglets. The injected embryos (n = 209) were endoscopically transferred into the uterine horns of 11 recipient gilts. Tissue analysis from 49 fetuses and eighteen liveborn piglets for PGC contribution in chimeras was carried out using PCR analysis for the presence of the marker transgene. Thirty‐two fetuses showed detectable chimerism in up to five out of 12 tissues analyzed. Skin samples from eight piglets were positive for the transgene, four of them displayed coat colour chimerism. Mol. Reprod. Dev. 54:244–254, 1999. © 1999 Wiley‐Liss, Inc.