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Experimental varicocoele in rats affects mechanisms that control expression and function of the androgen receptor

机译:大鼠实验性精索静脉曲张影响控制雄激素受体表达和功能的机制

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Varicocoele is an important cause of male infertility. Normal male reproductive function and fertility depends on a delicate balance between androgen receptor (AR) and the classic oestrogen receptors ESR1 (ER alpha) and ESR2 (ER beta). Using a model of surgically induced varicocoele in rats, this study aimed to investigate the effects of varicocoele on the expression of AR, ESR1, ESR2 and G-protein coupled oestrogen receptor (GPER). Varicocoele did not affect the mRNA and protein expression of ESR1 and ESR2 in both testes. Varicocoele did not affect the mRNA and protein expression of GPER in the right testis, but slightly reduced the mRNA and increased the protein levels in the left testis. Varicocoele did not affect the mRNA for AR, but reduced the protein levels in both testes. A proteomic approach was used in an attempt to find differentially expressed targets with possible correlation with AR downregulation. Varicocoele caused the differential expression of 29 proteins. Six proteins were upregulated, including the receptor for activated C kinase 1 (RACK1), and 23 were downregulated, including dihydrolipoamide dehydrogenase, alpha-enolase and pyrophosphatase 1. Western blot analysis confirmed that varicocoele upregulated the expression of RACK1, a protein involved with tyrosine phosphorylation and regulation of AR transcriptional activity, AR metabolism and dynamics of the blood-testis barrier. In conclusion, this study suggests that varicocoele affects mechanisms that control AR expression and function. This regulation of AR may play an important role in the varicocoele-induced testicular dysfunction. Furthermore, varicocoele downregulates several other proteins in the testis that may be useful markers of spermatozoa function and male infertility.
机译:精索静脉曲张是男性不育的重要原因。正常的男性生殖功能和生育能力取决于雄激素受体(AR)与经典雌激素受体ESR1(ER alpha)和ESR2(ER beta)之间的微妙平衡。本研究使用大鼠手术诱发的精索静脉曲张模型,旨在研究精索静脉曲张对AR,ESR1,ESR2和G蛋白偶联雌激素受体(GPER)表达的影响。精索静脉曲张在两个睾丸中均不影响ESR1和ESR2的mRNA和蛋白表达。精索静脉曲张不会影响右侧睾丸中GPER的mRNA和蛋白质表达,但会稍微降低左侧睾丸中的mRNA和增加蛋白质水平。精索静脉曲张不会影响AR的mRNA,但会降低两个睾丸中的蛋白质水平。蛋白质组学方法被用于寻找与AR下调可能相关的差异表达靶标。精索静脉曲张引起29种蛋白质的差异表达。六种蛋白被上调,包括激活的C激酶1(RACK1)的受体,而23种被下调,包括二氢脂酰胺脱氢酶,α-烯醇酶和焦磷酸酶1。蛋白质印迹分析证实精索静脉曲张上调了与酪氨酸有关的蛋白RACK1的表达。磷酸化和调节AR转录活性,AR代谢和血液-睾丸屏障的动力学。总之,这项研究表明,精索静脉曲张影响控制AR表达和功能的机制。 AR的这种调节可能在精索静脉曲张引起的睾丸功能障碍中起重要作用。此外,精索静脉曲张会下调睾丸中的其他几种蛋白质,这些蛋白质可能是精子功能和男性不育的有用标志。

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