TNFα stimulates the proliferation of immature Sertoli cells by attenuating UPS‐degradation of cyclin D1 and leads to the delay of BTB maturation in pubertal rats

Abstract

Backgrounds The Sertoli cell that plays a vital role during spermatogenesis is a known target of physiological and pathological factors affecting testicular development. Tumor necrosis factor alpha (TNFα) participates in the blood–testis barrier reconstruction, cell apoptosis, and inflammatory response by recognizing receptors on Sertoli cell. TNFα has also been shown to induce the proliferation of immature Sertoli cell in vitro, yet the mechanism still remains unclarified. Objectives This study was designed to investigate the effect of TNFα on blood–testis barrier development during puberty and the underlying mechanisms of TNFα‐induced immature Sertoli cell proliferation. Materials and methods Immature male Sprague–Dawley rats of postnatal day 12 were intraperitoneally injected with TNFα. Biotin‐labeled method was used to detect permeability of the developing blood–testis barrier after TNFα treatment, and the distribution of occludin and junctional adhesion molecule‐A (JAM‐A) were detected by immunofluorescence. Sertoli cells isolated from Sprague–Dawley rats of postnatal day 10 were cultured in vitro and treated with TNFα. Cell proliferation rate was reflected by Cell Counting Kit‐8 (CCK‐8) and 5‐ethynyl‐2'‐deoxyuridine (EdU) assay. Immunoblot and quantitative polymerase chain reaction were used to detect the expression of proliferating cell nuclear antigen, Fbxo4, and cyclin D1. Immunoprecipitation was used to detect the ubiquitination of cyclin D1 and the interaction between Fbxo4 and cyclin D1. Ammonium pyrrolidinedithiocarbamate (PDTC) was applied to detect the effect of nuclear factor kappaB (NFκB) activity inhibition on TNFα‐induced Sertoli cell proliferation. The adenoviral recombinant plasmid containing rat Fbxo4 gene was constructed to investigate the effect of Fbxo4 overexpression on Sertoli cell proliferation promoted by TNFα. Results The in vivo experiment revealed a significant delay of blood–testis barrier maturation in pubertal rats caused by exogenous TNFα. TNFα (10 ng/ml) treatment in vitro was found to promote the proliferation of immature Sertoli cells, accompanied with increased NFκB activity and cyclin D1 protein level. The level of Fbxo4 and ubiquitination of cyclin D1 were decreased after TNFα treatment. Inhibitor of NFκB or overexpression of Fbxo4 could both reverse the TNFα‐induced proliferation of immature Sertoli cells, meanwhile restore the ubiquitin–proteasome system‐dependent degradation of cyclin D1. Overexpression of Fbxo4 could not affect the activation of NFκB caused by TNFα. Conclusion These results indicate that TNFα inhibits the ubiquitination and degradation of cyclin D1 through the NFκB pathway, thereby promoting the proliferation of immature Sertoli cell in vitro and inducing the delay of blood–testis barrier maturation in pubertal rats.

Oxidative Stress, Cytotoxic and Inflammatory Effects of Azoles Combinatorial Mixtures in Sertoli TM4 Cells

“…They are also essential for the testis because of their production of follicle-stimulating hormone receptor (FSHR) and the androgen-binding protein (ABP) [ 34 ], and crucial for their direct implication in the blood–testis barrier (BTB) and in the release of various immunomodulatory factors [ 35 ]. In this context, a high level of proinflammatory cytokines produced by SCs, especially tumor necrosis factor-alpha (TNF-α), affects BTB functions, thereby leading to the impairment of spermatogenesis [ 36 , 37 , 38 , 39 , 40 ]. In performing their task, SCs also regulate and maintain the appropriate cellular redox status of sperm cells that exhibit a high ROS accumulation.…”