首页> 外文期刊>The Tohoku Journal of Experimental Medicine >Coexpression of menin and JunD during the duct cell differentiation in mouse submandibular gland.
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Coexpression of menin and JunD during the duct cell differentiation in mouse submandibular gland.

机译:在小鼠下颌腺导管细胞分化过程中,menin和JunD的共表达。

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In the submandibular gland (SMG) of mice, a duct portion called the granular convoluted tubule (GCT) is developed preferentially in males with puberty. This sexual dimorphism is androgen-dependent, but the underlying molecular mechanisms are unclear. We have demonstrated that the expression of a transcription factor JunD is regulated in association with the androgen-induced differentiation of GCT cells from striated duct (SD) cells. Menin, a nuclear protein encoded by the MEN1 tumor-suppressor gene, is known to bind JunD, thereby inhibiting its activity. In the present study, we examined the expression of menin in the mouse SMG by use of Northern blotting, Western blotting, and immunohistochemistry. Immunoreactivity for menin was higher in the female than male gland, and localized to the nuclei of intercalated duct cells and a subpopulation of SD cells. In contrast, GCT cells in males appeared negative for menin. The levels of menin in the SMG were increased with castration in males and decreased by repeated administration of testosterone to females or to castrated males. After a single administration of testosterone to females, many SD cells newly gained nuclear menin, which was lost as the cells converted to GCT cells by 48 hrs. These patterns of the expression and localization of menin were quite similar to those of JunD. Furthermore, the coimmunoprecipitation analysis of the SMG homogenates indicated that menin binds JunD in vivo. The present study suggests that the JunD-menin complex plays significant roles in the androgen-dependent differentiation of the duct system in the mouse SMG.
机译:在小鼠的下颌下腺(SMG)中,优先在青春期的雄性体内发育出称为颗粒回旋小管(GCT)的导管部分。这种二态性是雄激素依赖性的,但是潜在的分子机制尚不清楚。我们已经证明,转录因子JunD的表达与雄激素诱导的GCT细胞从横纹管(SD)细胞分化有关。 Menin是由MEN1肿瘤抑制基因编码的核蛋白,已知会结合JunD,从而抑制其活性。在本研究中,我们通过使用Northern印迹,Western印迹和免疫组化检查了小鼠SMG中menin的表达。雌性对menin的免疫反应性高于雄性,并定位于插层导管细胞和SD细胞亚群的细胞核。相反,男性中的GCT细胞对脑膜蛋白呈阴性。男性去势时SMG中的menin水平随男性去势而增加,而对女性或去势男性反复施用睾丸激素则降低。对雌性小鼠单次施用睾丸激素后,许多SD细胞新获得了核menin,当细胞在48小时内转化为GCT细胞时,它们就会丢失。 Menin的这些表达和定位模式与JunD非常相似。此外,对SMG匀浆的共免疫沉淀分析表明,menin在体内与JunD结合。本研究表明,JunD-menin复合物在小鼠SMG的导管系统的雄激素依赖性分化中起着重要作用。

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