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六价铬的雄性生殖毒性:在睾丸分化的关键窗口期子宫内暴露于六价铬会抑制成年F代子代大鼠支持细胞紧密连接蛋白和激素受体的表达。

Male reproductive toxicity of CrVI: In-utero exposure to CrVI at the critical window of testis differentiation represses the expression of Sertoli cell tight junction proteins and hormone receptors in adult F progeny rats.

作者信息

Kumar Kathiresh M, Aruldhas Mariajoseph Michael, Banu Sheerin L, Sadasivam Balaji, Vengatesh Ganapathy, Ganesh Karthik M, Navaneethabalakrishnan Shobana, Navin Ajith Kumar, Michael Felicia Mary, Venkatachalam Sankar, Stanley Jone A, Ramachandran Ilangovan, Banu Sakhila K, Akbarsha Mohammad Abdulkader

机构信息

Department of Endocrinology and Anatomy, Dr. ALM Post-Graduate Institute of Basic Medical Sciences, University of Madras, Taramani Campus, Chennai 600113, India; Department of Clinical and Translational Sciences, Robert C. Byrd Biotech Science Centre, Marshall University, Huntington, WV 25701, USA.

Department of Endocrinology and Anatomy, Dr. ALM Post-Graduate Institute of Basic Medical Sciences, University of Madras, Taramani Campus, Chennai 600113, India.

出版信息

Reprod Toxicol. 2017 Apr;69:84-98. doi: 10.1016/j.reprotox.2017.02.007. Epub 2017 Feb 10.

Abstract

The effect of gestational exposure to CrVI (occupational/environmental pollutant and target to Sertoli cells(SC)) was tested in a rat model during the testicular differentiation from the bipotential gonad may interrupt spermatogenesis by disrupting SC tight junctions(TJ) and it's proteins and hormone receptors. Pregnant Wistar rats were exposed to 50/100/200ppm CrVI through drinking water during embryonic days 9-14. On Postnatal day 120, testes were subjected to ion exchange chromatographic analysis and revealed increased level of CrIII in SCs and germ cells, serum and testicular interstitial fluid(TIF). Microscopic analyses showed seminiferous tubules atrophy and disruption of SC TJ, which also recorded decreased testosterone in TIF. mRNA and Protein expression analyses attested decreased level of Fshr, Ar, occludin and claudin-11 in SCs. Immunofluorescent detection revealed weak signal of TJ proteins. Taken together, we concluded that gestational exposure to CrVI interferes with the expression of SC TJ proteins due to attenuated expression of hormone receptors.

摘要

在大鼠模型中,研究了孕期暴露于六价铬(职业/环境污染物,对支持细胞(SC)有靶向作用)对睾丸从双潜能性腺分化过程的影响,六价铬可能通过破坏支持细胞紧密连接(TJ)及其蛋白质和激素受体来干扰精子发生。在胚胎期第9至14天,将怀孕的Wistar大鼠通过饮用水暴露于50/100/200ppm的六价铬中。在出生后第120天,对睾丸进行离子交换色谱分析,结果显示支持细胞、生殖细胞、血清和睾丸间质液(TIF)中的三价铬水平升高。显微镜分析显示生精小管萎缩和支持细胞紧密连接破坏,同时TIF中的睾酮水平也降低。mRNA和蛋白质表达分析证实支持细胞中促卵泡激素受体(Fshr)、雄激素受体(Ar)、闭合蛋白和Claudin-11的水平降低。免疫荧光检测显示紧密连接蛋白信号减弱。综上所述,我们得出结论,孕期暴露于六价铬会由于激素受体表达减弱而干扰支持细胞紧密连接蛋白的表达。

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