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Biology of Reproduction 66, 450-457 (2002)
© 2002 Society for the Study of Reproduction, Inc.


Regular Article

Tumor Necrosis Factor {alpha} Enhances Oocyte/Follicle Apoptosis in the Neonatal Rat Ovary1

Leisa J. Morrisona, and Jennifer L. Marcinkiewicz2,a

a Department of Biological Sciences, Kent State University, Kent, Ohio 44242-0001

Tumor necrosis factor {alpha} (TNF{alpha}) is a multifunctional cytokine present in oocytes and macrophages in the neonatal rat ovary. The presence of both TNF{alpha} and its receptors in the neonatal rat ovary suggests a potential role for it in follicle assembly or oocyte atresia. Previous studies have provided support for effects of TNF{alpha} on isolated granulosa and theca cells and intact follicles; however, to our knowledge, this is the first study to investigate the effects of TNF{alpha} on the earliest stages of follicular development. Effects of TNF{alpha} on oocyte/follicle number and apoptosis were investigated using an ovarian organ-culture system that supported assembly of primordial follicles in vitro. Ovaries were collected on the day of birth and treated with TNF{alpha} (0, 0.1, 1.0, 10, or 50 ng/ml), a function-blocking TNF{alpha} antibody (5 µg/ml), or control immunoglobulin (Ig) G. At 1 ng/ml, TNF{alpha} decreased follicle and oocyte numbers during 3 days of culture, whereas higher (10 and 50 ng/ml) or lower (0.1 ng/ml) doses had no effect. Treatment with TNF{alpha} antibodies increased the number of oocytes and follicles compared to nonspecific IgG control. To determine whether the decreased oocyte/follicle numbers were due to an apoptotic effect of TNF{alpha}, apoptosis was examined by DNA laddering. At 1 ng/ml, TNF{alpha} increased apoptotic DNA laddering twofold, with no significant effect from lower or higher doses. The cells undergoing apoptosis, as determined by in situ end-labeling, were oocytes, interstitial cells, and granulosa cells. These findings suggest that TNF{alpha} may be involved in oocyte atresia that normally occurs during the perinatal period.

First decision: 11 May 2001.

1 Supported by NIH grant 1-R15-HD34252-01 (to J.L.M.) and by Sigma Xi Grants-in-Aid of Research (to L.J.M.).

2 Correspondence: Jennifer L. Marcinkiewicz, Box 5190, Department of Biological Sciences, Kent State University, Kent, OH 44242-0001. FAX: 330 672 3713; jmarcink{at}kent.edu




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