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通过cDNA微阵列分析鉴定GH3细胞系中的雌激素反应基因。

Identification of estrogen-responsive genes in the GH3 cell line by cDNA microarray analysis.

作者信息

Fujimoto Nariaki, Igarashi Katsuhide, Kanno Junn, Inoue Tohru

机构信息

Department of Developmental Biology, Research Institute for Radiation Biology and Medicine (RIRBM), Hiroshima University,1-2-3 Kasumi, Minami-ku, Hiroshima 734-8553, Japan.

出版信息

J Steroid Biochem Mol Biol. 2004 Jul;91(3):121-9. doi: 10.1016/j.jsbmb.2004.02.006.

Abstract

To identify estrogen-responsive genes in somatolactotrophic cells of the pituitary gland, a rat pituitary cell line GH3 was subjected to cDNA microarray analysis. GH3 cells respond to estrogen by growth as well as prolactin synthesis. RNAs extracted from GH3 cells treated with 17beta-estradiol (E2) at 10(-9) M for 24 h were compared with the control samples. The effect of an antiestrogen ICI182780 was also examined. The array analysis indicated 26 genes to be up-regulated and only seven genes down-regulated by E2. Fourteen genes were further examined by real-time RT-PCR quantification and 10 were confirmed to be regulated by the hormone in a dose-dependent manner. Expression and regulation of these genes were then examined in the anterior pituitary glands of female F344 rats ovariectomized and/or treated with E2 and 8 out of 10 were again found to be up-regulated. Interestingly, two of the most estrogen-responsive genes in GH3 cells were strongly dependent on E2 in vivo. #1 was identified as calbindin-D9k mRNA, with 80- and 118-fold induction over the ovariectomized controls at 3 and 24 h, respectively, after E2 administration. #2 was found to be parvalbumin mRNA, with 30-fold increase at 24 h. Third was c-myc mRNA, with 4.5 times induction at 24 h. The levels were maintained after one month of chronic E2 treatment. Identification of these estrogen-responsive genes should contribute to understating of estrogen actions in the pituitary gland.

摘要

为了鉴定垂体生长催乳素细胞中的雌激素反应基因,对大鼠垂体细胞系GH3进行了cDNA微阵列分析。GH3细胞对雌激素有生长反应以及催乳素合成反应。将用10(-9)M 17β-雌二醇(E2)处理24小时的GH3细胞提取的RNA与对照样品进行比较。还检测了抗雌激素ICI182780的作用。阵列分析表明,有26个基因被E2上调,只有7个基因被下调。通过实时RT-PCR定量进一步检测了14个基因,其中10个被证实受该激素剂量依赖性调节。然后在卵巢切除和/或用E2处理的雌性F344大鼠的垂体前叶中检测这些基因的表达和调节,发现10个中有8个再次被上调。有趣的是,GH3细胞中两个对雌激素反应最强的基因在体内强烈依赖E2。#1被鉴定为钙结合蛋白-D9k mRNA,在给予E2后3小时和24小时,分别比卵巢切除对照诱导80倍和118倍。#2被发现是小白蛋白mRNA,在24小时时增加30倍。第三个是c-myc mRNA,在24小时时诱导4.5倍。慢性E2处理一个月后水平维持不变。这些雌激素反应基因的鉴定应有助于理解雌激素在垂体中的作用。

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