Gong Yi, Pan Xuping, Huang Yufeng, Gao Zishen, Yu Hongxia, Han Xiaodong
Immunology and Reproductive Biology Laboratory, Medical School, Nanjing University, Nanjing 210093, P R China.
Toxicol Lett. 2008 Dec 15;183(1-3):10-20. doi: 10.1016/j.toxlet.2008.08.011. Epub 2008 Sep 2.
Nonylphenol (NP) is a representative endocrine disruptor that has an adverse effect on male reproduction and posses direct hazard to Sertoli cells, but the mechanism remains incompletely elucidated. In the present study, based on the structural comparability and high affinity between NP and membrane phospholipid molecules, we tested the hypothesis that entrance of NP into Sertoli cells would alter membrane biophysical characteristics and biochemical functions. First, we used gas chromatography-mass spectrometry (GC-MS) to investigate the distribution and pharmacokinetics of NP in Sertoli cells with the result revealing that NP could penetrate plasma membrane of Sertoli cells. Meanwhile, Sertoli cells treated with NP exhibited abnormal membrane potential; that is an early depolarization following short treatment and hyperpolarization after longer treatment with the highest concentration of NP. Studies on the membrane dynamics indicated that the NP exposure rendered increased membrane fluidity and decreased microviscosity and molecular order. The result of lactate dehydrogenase (LDH) leakage assay demonstrated that NP increased membrane permeability in time-dose-dependent manners. Atomic force microscopic (AFM) imaging was applied to examine the membrane topography, and the images showed that NP treatment caused disturbance of membrane topography. The activities of plasma membrane Ca(2+)-ATPase, Ca(2+)-Mg(2+)-ATPase and Na(+)-K(+)-ATPase were also changed following NP exposure. However, FSH receptor as an important membrane protein was not significantly altered. All the above changes led to the disturbed intracellular Ca(2+) homeostasis which was an important signal triggering apoptosis. Hence, cellular membranes represented a plausible target for NP-induced cytotoxicity.
壬基酚(NP)是一种典型的内分泌干扰物,对雄性生殖有不良影响,对支持细胞具有直接危害,但其作用机制仍未完全阐明。在本研究中,基于NP与膜磷脂分子之间的结构相似性和高亲和力,我们验证了以下假设:NP进入支持细胞会改变膜的生物物理特性和生化功能。首先,我们使用气相色谱 - 质谱联用仪(GC-MS)研究NP在支持细胞中的分布和药代动力学,结果显示NP能够穿透支持细胞的质膜。同时,用NP处理的支持细胞表现出异常的膜电位;即在短时间处理后早期去极化,在用最高浓度的NP长时间处理后超极化。对膜动力学的研究表明,NP暴露使膜流动性增加,微粘度和分子有序性降低。乳酸脱氢酶(LDH)泄漏试验结果表明,NP以时间 - 剂量依赖的方式增加膜通透性。应用原子力显微镜(AFM)成像检查膜表面形貌,图像显示NP处理导致膜表面形貌紊乱。NP暴露后,质膜Ca(2 +)-ATP酶、Ca(2 +)-Mg(2 +)-ATP酶和Na(+)-K(+)-ATP酶的活性也发生了变化。然而,作为一种重要膜蛋白的促卵泡激素(FSH)受体没有明显改变。上述所有变化导致细胞内Ca(2 +)稳态紊乱,这是触发细胞凋亡的重要信号。因此,细胞膜是NP诱导细胞毒性的一个合理靶点。