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Vertebrate reproductive science and technology
RESEARCH ARTICLE

Male germ cell transplantation in livestock

J. R. Hill A C and I. Dobrinski B
+ Author Affiliations
- Author Affiliations

A CSIRO Livestock Industries, New England Highway, Armidale, NSW 2350, Australia.

B Center for Animal Transgenesis and Germ Cell Research, University of Pennsylvania School of Veterinary Medicine, New Bolton Center, Kennett Square, PA 19348, USA.

C Corresponding author. Email: jon.hill@csiro.au

Reproduction, Fertility and Development 18(2) 13-18 https://doi.org/10.1071/RD05123
Submitted: 21 September 2005  Accepted: 21 September 2005   Published: 14 December 2005

Abstract

Male germ cell transplantation is a powerful approach to study the control of spermatogenesis with the ultimate goal to enhance or suppress male fertility. In livestock animals, applications can be expanded to provide an alternative method of transgenesis and an alternative means of artificial insemination (AI). The transplantation technique uses testis stem cells, harvested from the donor animal. These donor stem cells are injected into seminiferous tubules, migrate from the lumen to relocate to the basement membrane and, amazingly, they can retain the capability to produce donor sperm in their new host. Adaptation of the mouse technique for livestock is progressing, with gradual gains in efficiency. Germ cell transfer in goats has produced offspring, but not yet in cattle and pigs. In goats and pigs, the applications of germ cell transplantation are mainly in facilitating transgenic animal production. In cattle, successful male germ cell transfer could create an alternative to AI in areas where it is impractical. Large-scale culture of testis stem cells would enhance the use of elite bulls by providing a renewable source of stem cells for transfer. Although still in a developmental state, germ cell transplantation is an emerging technology with the potential to create new opportunities in livestock production.

Extra keywords: cattle, goats, pigs, stem cells, testis.


Acknowledgments

Work from the authors’ laboratories was supported by CSIRO Flagship project ‘Engineering new breeding systems’ (to JRH) and R01 RR017359–04 (NCRR/NIH) and R41 HD044780–01 (NICHD/NIH) (to ID).


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