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Biology of Reproduction 63, 1014-1023 (2000)
© 2000 Society for the Study of Reproduction, Inc.


ARTICLES

Development of Mouse and Rat Oocytes in Chimeric Reaggregated Ovaries after Interspecific Exchange of Somatic and Germ Cell Components1

John J. Eppig2,a, and Karen Wiggleswortha

a The Jackson Laboratory, Bar Harbor, Maine 04609

The germ cell and somatic cell compartments of newborn rat and mouse ovaries, which contain only primordial stage follicles, were completely exchanged and reaggregated to produce xenogeneic chimeric ovaries. The reaggregated ovaries were grafted beneath the renal capsules of ovariectomized SCID mice to develop for periods up to 21 days. Xenogeneic follicles developed with essentially normal morphological characteristics. Both rat and mouse oocytes with species-specific characteristics grew within follicles that were composed of somatic cells exclusively of the alternative species. Rat oocytes grown in mouse follicles became competent to resume meiosis, and progressed to metaphase II when they were removed from follicles and cultured. In addition, mouse oocytes grown in rat follicles underwent fertilization and preimplantation development in vitro, and developed to term after embryos were transferred to pseudopregnant mouse foster mothers. Therefore, despite an estimated 11 million years of divergent evolution, oocytes and somatic cells of rat and mouse ovaries can be exchanged and can produce functional oocytes. It is concluded that factors involved in oocyte-somatic cell interactions necessary to support oocyte development and appropriate differentiation of the oocyte-associated granulosa cells are conserved between rats and mice. Moreover, although granulosa cells play important roles in oocyte development, the development of species-specific characteristics of oocytes occurs without apparent modification by a xenogeneic follicular environment.

First decision: 3 May 2000.

1 This research was funded by the National Institute of Child Health and Human Development (NICHD) through NIH grant HD23839. The development of culture systems was supported by The National Cooperative Program on Non-Human In Vitro Fertilization and Preimplantation Development, which was funded by NICHD through cooperative agreement HD21970. The scientific services of the Jackson Laboratory receive support from a Cancer Center Core Grant (CA34196) from the National Cancer Institute.

2 Correspondence. FAX: 207 288 6073; jje{at}jax.org




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