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大鼠子宫中差异调节的即刻早期基因

Differentially regulated immediate early genes in the rat uterus.

作者信息

Bigsby R M, Li A

机构信息

Department of Obstetrics and Gynecology, Indiana University School of Medicine, Indianapolis 46202-5196.

出版信息

Endocrinology. 1994 Apr;134(4):1820-6. doi: 10.1210/endo.134.4.8137748.

Abstract

Estrogen stimulates cellular proliferation in the luminal epithelium, stroma, and smooth muscle of immature rat uterus. Progesterone administered concurrently with estrogen blocks the stimulatory effect of estrogen specifically in the epithelium, whereas progesterone administered alone stimulates proliferation in the endometrial stroma and myometrium. The present studies determined the effects of estrogen and progesterone on expression of the growth-associated, immediate early genes c-fos, c-jun, and jun-B in the luminal epithelium of the uterus. Hormonal effects were quantitated by Northern analysis of RNA extracted directly from the uterine luminal epithelium. Estrogen stimulated c-fos and jun-B expression, but repressed c-jun mRNA levels in the epithelium. In contrast, when whole organ RNA extracts were analyzed, estrogen increased mRNA levels for all three genes. Although progesterone administered alone showed no effect on mRNA levels in either epithelial or whole uterus extracts, it did attenuate the estrogen-induced increase in c-fos mRNA by 50% in whole uterus extracts and by 23% in epithelial extracts. The estrogen-induced increase in epithelial jun-B mRNA was not affected by progesterone pretreatment. Thus, in the immature rat uterus, no simple correlation exists between cellular proliferation and increased expression of the genes studied. However, progesterone completely blocked the repressive effect of estrogen on epithelial c-jun, suggesting a link between decreased c-jun expression and induction of cell proliferation in the uterine luminal epithelium. Estrogen repression of epithelial c-jun expression was hormone specific and sensitive to antiestrogen blockade. After estrogen treatment, epithelial c-jun mRNA decreased with a rate similar to its half-life, as determined in primary cultures of rat uterine cells. These results suggest that estrogen, acting through its receptor, directly represses transcription of c-jun in the uterine epithelium. Differences in hormonal regulation of immediate early genes between epithelial and nonepithelial uterine tissues probably results from tissue-specific transactivating factors that control the expression of these genes.

摘要

雌激素可刺激未成熟大鼠子宫腔上皮、基质和平滑肌细胞的增殖。与雌激素同时给予的孕酮可特异性地阻断雌激素对上皮细胞的刺激作用,而单独给予孕酮则可刺激子宫内膜基质和子宫肌层的增殖。本研究确定了雌激素和孕酮对子宫腔上皮中与生长相关的即刻早期基因c-fos、c-jun和jun-B表达的影响。通过对直接从子宫腔上皮提取的RNA进行Northern分析来定量激素效应。雌激素刺激了c-fos和jun-B的表达,但抑制了上皮细胞中c-jun mRNA的水平。相反,当分析全器官RNA提取物时,雌激素增加了所有这三个基因的mRNA水平。虽然单独给予孕酮对上皮或全子宫提取物中的mRNA水平没有影响,但它确实使全子宫提取物中雌激素诱导的c-fos mRNA增加减少了50%,使上皮提取物中减少了23%。雌激素诱导上皮jun-B mRNA的增加不受孕酮预处理的影响。因此,在未成熟大鼠子宫中,细胞增殖与所研究基因表达的增加之间不存在简单的相关性。然而,孕酮完全阻断了雌激素对上皮c-jun的抑制作用,这表明子宫腔上皮中c-jun表达的降低与细胞增殖的诱导之间存在联系。雌激素对上皮c-jun表达的抑制具有激素特异性且对抗雌激素阻断敏感。雌激素处理后,上皮c-jun mRNA以与其半衰期相似的速率下降,这是在大鼠子宫细胞原代培养中确定的。这些结果表明,雌激素通过其受体直接抑制子宫上皮中c-jun的转录。子宫上皮组织和非上皮组织之间即刻早期基因激素调节的差异可能是由控制这些基因表达的组织特异性反式激活因子引起的。

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