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首页> 外文期刊>Molecular and Cellular Endocrinology >Expression and characterization of androgen receptor coregulators, SRC-2 and HBO1, during human testis ontogenesis and in androgen signaling deficient patients
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Expression and characterization of androgen receptor coregulators, SRC-2 and HBO1, during human testis ontogenesis and in androgen signaling deficient patients

机译:雄激素受体调节剂SRC-2和HBO1在人睾丸癌变过程中和雄激素信号缺陷患者中的表达和特征

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摘要

Androgen receptor (AR) is essential for testicular physiology and spermatogenesis. SRC-2 and HBO1 are two AR coregulators yet their expression and roles in human testis are unknown. For the first time, we studied by immunohistochemistry and RT-PCR, the expression and distribution of these two coregulators during human testicular ontogenesis, in patients with altered AR signaling (Androgen insensitivity syndrome, AIS) and evaluated the functional impact of SRC-2 and HBO1 on AR signaling in a Sertoli cell context. SRC-2 was present in Sertoli cells at all developmental stages. HBO1 was barely or focally detected in the fetal testis yet its expression, in Sertoli and germ cells, drastically increased postnatally from early infancy to adulthood. In transient co-transfection studies we showed that SRC-2 induced, while HBO1 inhibited AR-mediated transactivation of reporter constructs in murine Sertoli SMAT1 cells. HBO1, but not SRC-2, expression was reduced in testes of patients with AIS compared to normal testes.
机译:雄激素受体(AR)对于睾丸生理和精子发生至关重要。 SRC-2和HBO1是两个AR调节剂,但在人类睾丸中的表达和作用尚不清楚。我们首次通过免疫组织化学和RT-PCR研究了这两种共调节因子在人睾丸本体发育过程中AR信号改变(雄激素不敏感综合征,AIS)患者中的表达和分布,并评估了SRC-2和SRC-2的功能影响。在Sertoli细胞环境中关于AR信号的HBO1。 SRC-2存在于所有发育阶段的Sertoli细胞中。 HBO1在胎儿睾丸中几乎没有或局部检测到,但从婴儿早期到成年后,其在睾丸支持细胞和生殖细胞中的表达急剧增加。在瞬时共转染研究中,我们显示了SRC-2诱导,而HBO1抑制了小鼠Sertoli SMAT1细胞中报告基因构建体的AR介导的反式激活。与正常睾丸相比,AIS患者的睾丸中HBO1而非SRC-2的表达降低。

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