Immunology and Reproduction Biology Laboratory, Medical School, Nanjing University, Nanjing, Jiangsu 210093, China.
Reprod Toxicol. 2010 Nov;30(3):438-45. doi: 10.1016/j.reprotox.2010.06.003. Epub 2010 Jun 25.
In this study, our purpose is to analyze combined effects of nonyl phenol (NP) and di-n-butyl phthalate (DBP) for rat testicular Sertoli cell toxicity in vitro. Sertoli cells were isolated, purified, cultured, and identified with FSHR fluorescence staining. Then the purified Sertoli cells were treated with different doses of NP, DBP or NP+DBP. Although we did not find dramatic morphological changes, cell viability decreased significantly at high-dose NP and their mixture. The following Annexin V-PI staining demonstrated that DBP alone did not show apoptosis induction, the combination effect on apoptosis induction was due to NP, in addition, nucleus of Sertoli cell showed apoptosis morphological changes. In addition, increased LDH leakage was also observed in high-dose mixture. According to the above phenomena, we inferred that the combined effect of the two substances on Sertoli cell toxicity had an additive effect, and the induction of apoptosis may play an important role.
在这项研究中,我们的目的是分析壬基酚(NP)和邻苯二甲酸二丁酯(DBP)对体外大鼠睾丸支持细胞毒性的联合作用。使用 FSHR 荧光染色法分离、纯化、培养和鉴定支持细胞。然后用不同剂量的 NP、DBP 或 NP+DBP 处理纯化的支持细胞。虽然我们没有发现明显的形态变化,但高剂量 NP 和它们的混合物使细胞活力显著下降。随后的 Annexin V-PI 染色表明 DBP 单独不会诱导细胞凋亡,其诱导细胞凋亡的协同作用来自 NP,此外,支持细胞的细胞核显示出凋亡的形态变化。此外,在高剂量混合物中还观察到 LDH 漏出增加。根据上述现象,我们推断这两种物质对支持细胞毒性的联合作用具有相加效应,细胞凋亡的诱导可能发挥了重要作用。