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Biology of Reproduction 67, 327-333 (2002)
© 2002 Society for the Study of Reproduction, Inc.


Regular Article

Production of Cloned Cattle from In Vitro Systems

Erik J. Forsberga, Nikolai S. Strelchenkoa, Monica L. Augensteina, Jeffery M. Betthausera, Lynette A. Childsa, Kenneth J. Eilertsena, Joellyn M. Enosa, Todd M. Forsythea, Paul J. Goluekea, Richard W. Koppanga, Gail Langea, Tiffany L. Lesmeistera, Kelly S. Mallona, Greg D. Mella, Pavla M. Misicaa, Marvin M. Pacea, Martha Pfister-Genskowa, Gary R. Voelkera, Steven R. Watta, and Michael D. Bishop1,a

a Infigen, Inc., DeForest, Wisconsin 53532

The pregnancy initiation and maintenance rates of nuclear transfer embryos produced from several bovine cell types were measured to determine which cell types produced healthy calves and had growth characteristics that would allow for genetic manipulation. Considerable variability between cell types from one animal and the same cell type from different animals was observed. In general, cultured fetal cells performed better with respect to pregnancy initiation and calving than adult cells with the exception of cumulous cells, which produced the highest overall pregnancy and calving rates. The cell type that combined relatively high pregnancy initiation and calving rates with growth characteristics that allowed for extended proliferation in culture were fetal genital ridge (GR) cells. Cultured GR cells used in nuclear transfer and embryo transfer initiated pregnancies in 40% of recipient heifers (197), and of all recipients that received nuclear transfer embryos, 9% produced live calves. Cultured GR cells doubled as many as 85 times overall and up to 75 times after dilution to single-cell culture. A comparison between transfected and nontransfected cells showed that transfected cells had lower pregnancy initiation (22% versus 32%) and calving (3.4% versus 8.9%) rates.

First decision: 3 December 2001.

1 Correspondence: Michael D. Bishop, Infigen, Inc., 1825 Infinity Drive, DeForest, WI 53532. FAX: 608 846 0520; mbishop{at}infigen.com




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