Journal of Reproduction and Development · 2011 · 22 citations · 34 references
Life SciencesImmunologyPathobiologyAutoimmunityImmunopathologyReproductive ImmunologyCytokines In ReproductionImmunological InfertilityInterferon ResponsesMammalian ImmunologyTesticular FunctionTesticular ImmunologyCd4 Positive T Cell ResponsesImmune-mediated InfertilityImmune-mediated Male InfertilityImmunopathology Of Male InfertilityInflammatory Responses In TestisInterferon ProductionSeminiferous Epithelium InjuryTesticular Hormones
Experimental autoimmune orchitis (EAO) is one of the models of immunological male infertility. Murine EAO is CD4+T cell-dependent and classically induced by immunization with a testicular homogenate and adjuvants. We previously established that immunization with viable syngeneic testicular germ cells (TGC) can also induce murine EAO with no use of any adjuvant. Analyses of this EAO model have already revealed that cultured spleen cells of immunized mice secreted interferon (IFN)-γ and that treatment of the immunized mice with anti-IFN-γ monoclonal antibodies significantly suppressed the EAO. It is known that both IFN-γ and tumor necrosis factor (TNF)-α are representative cytokines of Th1 cells and exhibit local toxicity toward the seminiferous epithelium in vivo. However, changes in these two cytokines in EAO-affected testes have not yet been investigated. Therefore, in the present study, we investigated the expression of intratesticular IFN-γ and TNF- α mRNAs in TGC-induced EAO using real-time RT-PCR. The results demonstrated that the intratesticular mRNAs for both IFN-γ and TNF-α significantly increased, while other cytokines such as IL-1α, IL-1β, IL-6 and TGF-β did not show dramatic changes in the immunized mice. These results suggest that secretion of significant amounts of IFN-γ and TNF-α in situ contributes to the spermatogenic disturbance in EAO.
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Michelle K.Y. Siu, Will M. Lee, C. Yan Cheng · Endocrinology · 2002 · 242 citations · Full text
Expression of tumor necrosis factor-alpha in mouse spermatogenic cells.
Swapan K. De, H L Chen, J L Pace et al. · Endocrinology · 1993 · 205 citations