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Regulation of 3beta-hydroxysteroid dehydrogenase type 1 and type 2 gene expression and function in the human ovarian surface epithelium by cytokines

机译:细胞因子调节人卵巢表面上皮细胞中3β-羟类固醇脱氢酶1型和2型基因的表达和功能

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摘要

The human ovarian surface epithelium (hOSE) is a squamous-to-cuboidal layer that surrounds the ovary. hOSE undergoes injury and repair cycles as a result of ovulation-induced inflammation, an event relevant to the development of epithelial ovarian cancer (EOC). Locally produced steroids mediate the response to inflammation. 3beta-Hydroxysteroid dehydrogenase (3beta-HSD) drives the intracrine generation of progestogens and androgens that potentially affect cell survival and proliferation. We therefore investigated the regulation of 3beta-HSD along with downstream steroid signalling in hOSE. Double immunofluorescence of cultured primary hOSE cells confirmed the expression of 3beta-HSD protein Interleukin (IL). IL-1alpha treatment of primary cells to mimic ovulation-associated inflammation suppressed 3beta-HSD1 expression and stimulated 3beta-HSD2 mRNA (P < 0.001), without affecting total 3beta-HSD protein and activity or androgen or progesterone receptor (PR) mRNA levels. Conversely, IL-4 as a proxy for a post-ovulatory healing cytokine increased both 3beta-HSD transcripts, total protein and activity (P < 0.01). IL-4 also suppressed androgen receptor expression (P < 0.01) without affecting that of the PR, thereby potentially sustaining both progesterone biosynthesis and its underlying signalling in the ovarian surface. 3beta-HSD protein was immuhodetect-able in primary ascites of women who were diagnosed with EOC but both mRNA transcripts were diminished relative to normal cells (P < 0.05). Notably, this difference was countered by IL-4 treatment (P < 0.01). We conclude that stimulation by IL-4 could be physiologically relevant to post-ovutatory ovarian healing and suggest a novel therapeutic strategy for the activation of progesterone-associated apoptosis in ovarian cancer. Also, our results suggest an attenuation of 3beta-HSD expression in EOC although further studies are required for confirmation.
机译:人卵巢表面上皮(hOSE)是围绕卵巢的鳞状到立方的层。由于排卵诱导的炎症,hOSE经历了损伤和修复周期,这是与上皮性卵巢癌(EOC)发生有关的事件。局部产生的类固醇介导对炎症的反应。 3beta-羟基类固醇脱氢酶(3beta-HSD)驱动着孕激素和雄激素的内分泌生成,这可能会影响细胞存活和增殖。因此,我们研究了hOSE中3beta-HSD的调控以及下游类固醇信号传导。培养的原代hOSE细胞的双重免疫荧光证实了3beta-HSD蛋白白介素(IL)的表达。 IL-1alpha处理原代细胞以模拟与排卵相关的炎症抑制了3beta-HSD1表达并刺激了3beta-HSD2 mRNA(P <0.001),而没有影响总的3beta-HSD蛋白和活性或雄激素或孕激素受体(PR)mRNA水平。相反,作为排卵后愈​​合细胞因子的替代物,IL-4增加了3beta-HSD转录本,总蛋白和活性(P <0.01)。 IL-4还抑制了雄激素受体的表达(P <0.01),而没有影响PR的表达,从而潜在地维持了孕酮的生物合成及其在卵巢表面的潜在信号传导。 3beta-HSD蛋白在被诊断患有EOC的女性原发性腹水中是不可检测的,但相对于正常细胞,这两个mRNA转录物均减少(P <0.05)。值得注意的是,这种差异被IL-4治疗所抵消(P <0.01)。我们得出结论,IL-4的刺激可能与排卵后卵巢愈合在生理上有关,并提出了一种激活卵巢癌中孕激素相关凋亡的新治疗策略。同样,我们的结果表明EOC中3beta-HSD表达的减弱,尽管需要进一步的研究来确认。

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