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Effects of Medroxyprogesterone Acetate on Gene Expression in Myometrial Explants from Pregnant Women

机译:醋酸甲羟孕酮对孕妇子宫肌层外植体基因表达的影响

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Context: Progesterone is important physiologically and therapeutically to maintain uterine quiescence during pregnancy, in part through controlling myometrial gene expression.Objective: The objective of the study was to use expression microarray and quantitative reverse transcriptase-PCR (qRT-PCR) validation to determine the changes in gene expression induced by prolonged exposure of human myometrium to a synthetic progestogen.Design: Myometrial explants, obtained at elective cesarean section (n = 9), were maintained in culture, under 0.6 g tension, for 65 h in the presence of medroxyprogesterone acetate (100 nm) or vehicle. Expression array was performed using Illumina beadchip arrays. Approximately 30% of differentially expressed transcripts were validated in biological replicates (n = 10) by qRT-PCR.Results: The 114 significantly regulated transcripts were significantly enriched in inflammatory response ( P = 0.00001), growth factor activity ( P = 0.0004), and cytokine activity genes ( P = 0.008). Thirty-four transcripts were validated using qRT-PCR in explants obtained from 10 further women. There was very close agreement in the fold changes obtained by array and qRT-PCR (r~(2) = 0.9, P < 0.0001). We confirmed significant down-regulation of a number of genes that have been well characterized as progesterone sensitive ( IL-1B , IL-6 , PTGS2 , and GJA1 ). However, the top and sixth most down-regulated transcripts encoded two cytokines, IL-11 and IL-24 , respectively, not previously implicated in mediating the effects of progesterone in myometrium. Both were validated by qRT-PCR (4.3- and 2.2-fold down-regulated, both P < 0.001).Conclusions: Medroxyprogesterone acetate controls expression of multiple genes in myometrium, including many that have not previously been characterized as progestogen regulated in this tissue, including IL-11 and IL-24 . It is plausible that proteins encoded by some of these genes may have important but as yet uncharacterized effects in controlling human parturition.
机译:背景:孕酮在生理和治疗上对维持妊娠期间的子宫静止具有重要作用,部分是通过控制子宫肌层基因表达来进行的。目的:本研究的目的是使用表达微阵列和定量逆转录PCR(qRT-PCR)验证来确定设计:将在选择性剖宫产(n = 9)时获得的子宫肌层外植体在0.6 g张力下于甲氧孕酮存在下培养65 h。醋酸盐(100 nm)或媒介物。表达阵列使用Illumina的beadchip阵列进行。通过qRT-PCR在生物学重复中验证了大约30%的差异表达转录本(n = 10)。结果:114种显着调节的转录本在炎症反应(P = 0.00001),生长因子活性(P = 0.0004),和细胞因子活性基因(P = 0.008)。使用qRT-PCR在从另外10位女性获得的外植体中验证了34个转录本。通过阵列和qRT-PCR获得的倍数变化具有非常紧密的一致性(r〜(2)= 0.9,P <0.0001)。我们确认了许多基因的显着下调,这些基因已被很好地表征为孕激素敏感性(IL-1B,IL-6,PTGS2和GJA1)。但是,表达水平最高和排名第六的转录因子分别编码两种细胞因子IL-11和IL-24,以前并未参与介导孕激素在子宫内膜中的作用。两者均通过qRT-PCR验证(下调4.3倍和2.2倍,均P <0.001)。结论:醋酸甲羟孕酮可控制子宫内膜中多个基因的表达,包括许多以前尚未被该组织调节为孕激素的基因。 ,包括IL-11和IL-24。由这些基因中的一些编码的蛋白质可能在控制人类分娩中可能具有重要但尚未表征的作用,这似乎是合理的。

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