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Hum. Reprod. Advance Access published online on October 11, 2007

Human Reproduction, doi:10.1093/humrep/dem314
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© The Author 2007. Published by Oxford University Press on behalf of the European Society of Human Reproduction and Embryology. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

High oxygen atmosphere improves human follicle development in organ cultures of ovarian cortical tissues in vitro

Y. Morimoto1,3, Y. Oku1, M. Sonoda1, A. Haruki1, K. Ito1, S. Hashimoto1 and A. Fukuda2

1 The Centre for Reproductive Medicine and Infertility, IVF Namba Clinic, 1-17-28, Minami-horie, Nishi-ku, Osaka 550-0015, Japan 2 IVF Osaka Clinic, Osaka, Japan

3 Correspondence address. E-mail: york{at}ivfnamba.com

BACKGROUND: Obtaining mature human follicles from cultured ovarian tissue may be beneficial for clinical use for women who wish to preserve fertile competence. However, the methodology of culture such as culture condition and gas atmosphere has not been well established in humans. Therefore, we investigated the effect of oxygen concentration in organ culture in order to establish an ovarian tissue culture method.

METHODS: Ovarian tissue was obtained from 26–35-year-old women undergoing removal of a benign tumor (n = 12) or caesarean section (n = 16). The ovarian cortical tissues were cultured on a cell culture insert for 15 days under high (100%) and low (air, 20%) oxygen concentrations and then inspected for follicle development with light and electron microscopy. Estradiol and progesterone concentrations in the medium during culture were measured.

RESULTS: The ultrastructure and the function of hormone secretion in the cultured tissues were well preserved after organ culture. The follicles developing under high oxygen were larger and more matured than those developing under low oxygen (P < 0.05).

CONCLUSIONS: Human ovarian tissues can be cultured for 15 days under high oxygen concentration with the organ culture system used here. This technique could make it possible to utilize ovarian tissue for preservation of reproductive competence in cancer patients.

Key words: ovarian tissue/organ culture/in vitro maturation/follicle/oocyte

Submitted on May 5, 2007; resubmitted on August 6, 2007; accepted on August 28, 2007.


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