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(American Journal of Pathology. 2002;160:205-218.)
© 2002 American Society for Investigative Pathology

Regular Articles

Nuclear Factor-B Activation in Human Testicular Apoptosis

Virve Pentikäinen^*, Laura Suomalainen^*, Krista Erkkilä^*, Eeva Martelin^*, Martti Parvinen, Markku O. Pentikäinen and Leo Dunkel^*

From the Program for Developmental and Reproductive Biology,^*
Biomedicum Helsinki, and Hospital for Children and Adolescents, University of Helsinki, Helsinki; the Wihuri Research Institute,
Helsinki; and the Department of Anatomy,
University of Turku, Turku, Finland

Apoptotic cell death plays an important role in limiting testicular germ cell population during spermatogenesis and its dysregulation has been shown to be associated with male infertility. The growing evidence on the role of the transcription factor nuclear factor (NF)-B in controlling apoptosis prompted us to investigate NF-B activity in the normal human testis and its role in testis tissue undergoing excessive apoptosis in vitro. In electrophoretic mobility shift assays, low-level constitutive NF-B DNA-binding activity was found and, by immunostaining of the RelA and p50 NF-B subunits, was localized to Sertoli cell nuclei. During in vitro-induced testicular apoptosis, the Sertoli cell nuclear NF-B levels and whole seminiferous tubule NF-B DNA-binding activity increased previous detection of germ cells undergoing apoptosis. The anti-inflammatory drug sulfasalazine effectively suppressed stress-induced NF-B DNA binding and NF-B-mediated IB gene expression. Importantly, concomitantly with inhibiting NF-B, sulfasalazine blocked germ cell apoptosis. These results suggest that during testicular stress Sertoli cell NF-B proteins exert proapoptotic effects on germ cells, which raises the possibility that pharmacological inhibition of NF-B could be a therapeutic target in transient stress situations involving excessive germ cell death.

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