Zhang Wei, Shen Hua, Ma Long, Shen Baixin, Xu Zicheng, Wang Xinru
Department of Urology, First Affiliated Hospital of Nanjing Medical University, 210029 Nanjing, Jiangsu, China.
Toxicology. 2007 Oct 30;240(1-2):86-95. doi: 10.1016/j.tox.2007.07.021. Epub 2007 Aug 8.
To isolate and identify differentially expressed proteins in fetal rat testis following in utero exposure to di(nbutyl) phthalate (DBP).
We used the technique of proteomic analysis to compare the testis protein patterns obtained by two-dimensional gel electrophoresis from fetal rats of gestation day 19.
We found significant differences in protein spot intensities. Subsequently several of these variant protein spots were identified by mass spectrometry. Peroxiredoxin 6 (Prdx6) was one of them. Prdx6, which expressed a higher level in DBP-treated fetal rat testes compared with normal ones, is a member of the peroxiredoxins family (Prdxs). Recently, Prdx6 had been shown to be important in protecting cells from oxidative injury. Further, immunohistochemical analyses of fetal rat testes sections were made to determine the cellular distribution of this protein, consequently a strong Prdx6 staining was found out primarily in Leydig cells.
The present study had found several differentially regulated proteins and demonstrated the differential expression of Prdx6 in fetal rat testis following in utero exposure to DBP, when compared with controls. Combining the cellular location of Prdx6 and its function in other tissues, the results of this study could provide us with a possibility to interfere the reproductive toxicity of DBP for its specific antioxidant properties in testis tissues.
分离并鉴定宫内暴露于邻苯二甲酸二丁酯(DBP)的胎鼠睾丸中差异表达的蛋白质。
我们采用蛋白质组学分析技术,比较妊娠第19天胎鼠经二维凝胶电泳获得的睾丸蛋白质图谱。
我们发现蛋白质斑点强度存在显著差异。随后,通过质谱鉴定了其中几个变异蛋白质斑点。过氧化物酶体增殖物激活受体6(Prdx6)就是其中之一。与正常胎鼠睾丸相比,Prdx6在DBP处理的胎鼠睾丸中表达水平更高,它是过氧化物酶体增殖物激活受体家族(Prdxs)的成员之一。最近研究表明,Prdx6在保护细胞免受氧化损伤方面具有重要作用。此外,对胎鼠睾丸切片进行免疫组织化学分析以确定该蛋白的细胞分布,结果发现Prdx6主要在睾丸间质细胞中呈现强染色。
本研究发现了几种差异调节的蛋白质,并证明与对照组相比,宫内暴露于DBP的胎鼠睾丸中Prdx6存在差异表达。结合Prdx6的细胞定位及其在其他组织中的功能,本研究结果为我们利用其在睾丸组织中的特定抗氧化特性干预DBP的生殖毒性提供了可能性。