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Differential expression of peroxiredoxin 6, annexin A5 and ubiquitin carboxyl-terminal hydrolase isozyme L1 in testis of rat fetuses after maternal exposure to di-n-butyl phthalate

机译:母体暴露于邻苯二甲酸二正丁酯后大鼠胎儿睾丸中过氧化物酶6,膜联蛋白A5和泛素羧基末端水解酶同工酶L1的差异表达

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Objectives: To isolate and identify differentially expressed proteins in testis of rat fetuses after maternal exposure to di-n-butyl phthalate (DBP). Methods: Pregnant rats were daily treated by gavage with 1. ml/kg corn oil or 750. mg/kg DBP from GD14 to GD18. 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. Results: We found significant differences in protein spot intensities compared to control. Subsequently several of these variant protein spots were identified by mass spectrometry. Peroxiredoxin 6 (Prdx6), annexin A5 (AnxA5) and ubiquitin carboxyl-terminal hydrolase isozyme L1 (UchL1) were three of them, the differential expression of which were confirmed by western blotting. Further, immunohistochemical analyses of fetal rat testes sections were made to determine the cellular distribution of these proteins, consequently strong Prdx6 and AnxA5 stainings were found primarily in Leydig cells, while a weak UchL1 staining was found primarily in spermatogonium. Conclusions: The present study had found several differentially regulated proteins and demonstrated the differential expression of Prdx6, AnxA5 and UchL1 in fetal rat testis after maternal exposure to DBP, when compared with controls. Combining the cellular location of these proteins and their function in other tissues, the results of this study indicated that oxidative injury and abnormal apoptotic regulation might participate the formation of testicular dysgenesis in fetuses of dams exposed to DBP.
机译:目的:分离和鉴定母体暴露于邻苯二甲酸二正丁酯(DBP)后大鼠胎儿睾丸中差异表达的蛋白质。方法:每天用1. ml / kg玉米油或750. mg / kg DBP(从GD14到GD18)进行管饲法治疗妊娠大鼠。我们使用蛋白质组学分析技术,比较了通过二维凝胶电泳从妊娠19天的胎鼠获得的睾丸蛋白质模式。结果:与对照组相比,我们发现蛋白质斑点强度存在显着差异。随后,通过质谱鉴定了这些变体蛋白斑点中的几个。 Peroxiredoxin 6(Prdx6),膜联蛋白A5(AnxA5)和泛素羧基末端水解酶同工酶L1(UchL1)是它们中的三个,它们的差异表达通过蛋白质印迹法得以证实。此外,对胎儿大鼠睾丸切片进行了免疫组织化学分析,以确定这些蛋白质的细胞分布,因此,主要在睾丸间质细胞中发现强Prdx6和AnxA5染色,而主要在精子生殖细胞中发现弱UchL1染色。结论:本研究发现了几种差异调节的蛋白质,并证明了与对照相比,母体暴露于DBP后的胎鼠睾丸中Prdx6,AnxA5和UchL1的差异表达。结合这些蛋白质的细胞位置及其在其他组织中的功能,这项研究的结果表明,氧化损伤和异常的细胞凋亡调节可能参与了暴露于DBP的大坝胎儿的睾丸发育不全的形成。

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