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首页> 外文期刊>Cell death & disease. >Cross-talk between autophagy and apoptosis regulates testicular injury/recovery induced by cadmium via PI3K with mTOR-independent pathway
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Cross-talk between autophagy and apoptosis regulates testicular injury/recovery induced by cadmium via PI3K with mTOR-independent pathway

机译:自噬和细胞凋亡之间的串扰调节镉通过与MTOR的途径通过PI3K诱导的睾丸损伤/回收

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摘要

Autophagy and apoptosis are two major modes of cell death. A balanced interplay between both is vital for phagocytic clearance of apoptotic testicular cells. Here, generating a SD rats model-treated with cadmium (Cd) to mimic environmental exposure on human, we show that autophagy and apoptosis present synchronous change trends in Cd-induced testicular injury/self-recovery. Further, the cross-talk of autophagy and apoptosis is investigated in four testicular cell lines (GC-1/GC-2/TM3/TM4 cells) respectively. Results reveal that Cd-exposure for five consecutive weeks induces reproductive toxicity in male rats. After one cycle of spermatogenesis within 8 weeks without Cd, toxic effects are ameliorated significantly. In vitro, we find that PI3K inhibitor 3-MA regulates apoptosis by inhibiting autophagy with mTOR-independent pathway in Cd-treated testicular cells. Conclusively, cross-talk between autophagy and apoptosis regulates testicular injury/recovery induced by Cd via PI3K with mTOR-independent pathway.
机译:自噬和细胞凋亡是细胞死亡的两种主要模式。两者之间的平衡相互作用对于凋亡睾丸细胞的吞噬清除至关重要。这里,产生用镉(CD)进行模型处理的SD大鼠以模拟人体环境暴露,我们表明自噬和凋亡存在于CD诱导的睾丸损伤/自我恢复的同步变化趋势。此外,分别在四种睾丸细胞系(GC-1 / GC-2 / TM3细胞)中研究自噬和细胞凋亡的串扰。结果表明,连续五周的CD暴露会诱导雄性大鼠的生殖毒性。在没有Cd的8周内一个精子发生循环后,毒性效应显着改善。在体外,我们发现PI3K抑制剂3-MA通过在CD处理的睾丸细胞中抑制与MTOR的途径的自噬调节细胞凋亡。结论,自噬和细胞凋亡之间的串扰调节CD通过与MTOR的途径的PI3K诱导的睾丸损伤/回收。

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