The Rel/nuclear factor (NF)-kappaB family of transcription factors are important intracellular conveyors of extracellular signals in a number of systems. However, little is known of their roles in the specialized, hormonally regulated environment of the mammalian testis. In this study NF-kappaB p50 and p65 proteins were found to be constitutively present and active in the nucleus of Sertoli cells cultured from rat testis. In vivo, NF-kappaB proteins are present in the nucleus of Sertoli cells during all 14 (I-XIV) cyclical stages of spermatogenesis; however, nuclear NF-kappaB expression was elevated in stage XIV and remained high in stages I-VII. In contrast, NF-kappaB p50 and p65 subunits are transiently expressed in the nuclei of germ cells with peak levels found in pachytene spermatocytes during stages VII-XI and lower levels in stage I-VII spermatids. Tumor necrosis factor-alpha, which is produced by round spermatids in the testis, increased nuclear NF-kappaB binding activity when added to Sertoli cells. Stimulation of Sertoli cells with activators of the cAMP-protein kinase A (PKA) signaling pathway such as forskolin or FSH also increased NF-kappaB DNA binding activity. Consistent with the cellular localization studies, NF-kappaB was found to be activated as high basal levels of NF-kappaB-stimulated reporter gene expression were detected in transient transfection studies of Sertoli cells. Addition of tumor necrosis factor-alpha to Sertoli cells further stimulated kappaB enhancer-mediated transcription. These findings suggest that NF-kappaB proteins are stage specifically localized to Sertoli cell and spermatocyte nuclei and may play a role in the regulation of stage-specific gene expression during the process of spermatogenesis.
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Delfino et al. (1998) studied this question.
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