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Reproduction, Fertility and Development Reproduction, Fertility and Development Society
Vertebrate reproductive science and technology
RESEARCH ARTICLE

Induced parthenogenetic activation of oocytes of the marsupial Sminthopsis macroura

Marek Maleszewski A C and Lynne Selwood B
+ Author Affiliations
- Author Affiliations

A Department of Embryology, Institute of Zoology, Warsaw University, Miecznikowa 1, 02-096 Warszawa, Poland.

B Department of Zoology, University of Melbourne, Victoria 3010, Australia.

C To whom correspondence should be addressed. email: maleszewski@biol.uw.edu.pl

Reproduction, Fertility and Development 16(6) 599-604 https://doi.org/10.1071/RD03054
Submitted: 25 July 2003  Accepted: 26 April 2004   Published: 9 August 2004

Abstract

Maturation of marsupial oocytes in vitro, an important step in the analysis of early developmental events, has a low success rate and results from the artificial activation of oocytes, which may not include nuclear maturation. In Sminthopsis macroura, 24-h culture of advanced antral follicles in medium containing 10 μg mL−1 porcine pituitary luteinising hormone (LH) yielded 60% of mature polarised oocytes with the first polar body; follicles cultured in medium without LH yielded only immature oocytes. Parthenogenetic activation of follicular, oviducal or uterine oocytes occurred when a two-step protocol was used. Sixty-one oocytes, exposed to 10 μm calcium ionophore A23187 for 10 min followed by 10 μg mL−1 cycloheximide (protein synthesis inhibitor) for 5 h and then cultured for 20–24 h, were scored for signs of activation, namely extrusion of the second polar body and formation of the pronucleus. In each of 43 oocytes (70%), the extruded second polar body was present. Sixteen oocytes were analysed on slides after fixation and staining and, in 13 oocytes (81%) in this group, the female pronucleus was visible. No activation occurred following incubation of oocytes in medium containing Sr2+ for 5 h (n = 14), 8% ethyl alcohol solution for 8 or 12 min (n = 13) or 10 μm calcium ionophore A23187 (n = 13) for 10–20 min followed by culture for 20–24 h.


Acknowledgments

M. M. was a recipient of The Visiting Research Scholars Award from The University of Melbourne Collaborative Research Program 2002. This research was supported by grants to L. S. from The University of Melbourne Collaborative Research Program and the Australian Research Council.


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