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BOR - Papers in Press, published online ahead of print September 6, 2006.
Biol Reprod 2006, 10.1095/biolreprod.106.054833
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BIOLOGY OF REPRODUCTION 75, 916–923 (2006)
DOI: 10.1095/biolreprod.106.054833
© 2006 by the Society for the Study of Reproduction, Inc.


research-article

Identification of a Stage-Specific Permissive In Vitro Culture Environment for Follicle Growth and Oocyte Development1

Min Xu 3 4, Erin West 5, Lonnie D. Shea 5 6, and Teresa K. Woodruff 2 4 5 6 7

Center for Reproductive Science3 and Departments of Neurobiology and Physiology4 and Chemical and Biological Engineering,5 Northwestern University, Evanston, Illinois 60208 Robert H. Lurie Comprehensive Cancer Center6 and Department of Medicine,7 Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60611

ABSTRACT

The availability of viable oocytes is the limiting factor in the development of new reproductive techniques. Many attempts have been made to grow immature oocytes in vitro during recent decades. Recently, a modified alginate-based three-dimensional culture system was designed to support the growth and maturation of multilayered secondary follicles. This system was able to produce oocytes that successfully completed meiosis, fertilization, and development to the blastocyst stage. Subsequent attempts to culture two-layered secondary follicles were unsuccessful under the original conditions. Herein, we investigated the effect of alginate consistency on two-layered follicle growth and oocyte developmental competence by encapsulating follicles into alginate scaffolds of various concentrations. Although there were no significant differences in survival rates, 0.25% and 0.5% alginate supported more rapid growth of follicles and antrum formation compared with 1.5% and 1.0% alginate after 8 days of culture. Alginate scaffold concentration also affected the proliferation and differentiation of somatic cells (theca and granulosa cells), measured in terms of morphological changes, steroid profiles (androstenedione, estradiol, and progesterone), and specific molecular markers (Fshr, Lhcgr, and Gja1). Theca cell proliferation and steroid production were hindered in follicles cultured in 1.5% alginate. In vitro fertilization and embryo culture revealed that oocytes obtained from 0.25% alginate retained the highest developmental competence. Overall, the present study showed that the alginate scaffold consistency affects folliculogenesis and oocyte development in vitro and that the alginate culture system can and should be tailored to maximally support follicle growth depending on the size and stage of the follicles selected for culture.

follicular development, oocyte development


FOOTNOTES

1Supported by grant U54-HD41857 from the National Institutes of Health.

Correspondence: 2 Teresa K. Woodruff, Department of Neurobiology and Physiology, Northwestern University, 2205 Tech Drive, Hogan 4–150, Evanston, IL 60208. FAX: 847 491 2225; e-mail: tkw{at}northwestern.edu




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