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人胎盘细胞中葡萄糖转运蛋白1(Glut1)和c-fos基因的发育表达

Developmental expression of Glut1 glucose transporter and c-fos genes in human placental cells.

作者信息

Hauguel-de Mouzon S, Leturque A, Alsat E, Loizeau M, Evain-Brion D, Girard J

机构信息

Centre de Recherche sur l'Endocrinologie Moléculaire et le Développement, CNRS, Meudon-Belleuve, France.

出版信息

Placenta. 1994 Jan;15(1):35-46. doi: 10.1016/s0143-4004(05)80234-6.

Abstract

Glut1, the brain/erythrocyte glucose transporter is one major isoform of the human placenta and displays an age-specific pattern of expression with mRNA levels five-fold higher in first trimester than in term placenta. By contrast, the mRNA level of the insulin-regulatable glucose transporter Glut4 remains at the limit of detection throughout pregnancy indicating a very low expression of this isoform in the placenta. The nuclear proto-oncogenes c-fos and c-myc were also detectable in the human placenta, but c-fos only exhibited an age-specific pattern of expression with levels higher in third trimester than in term placenta. Primary cultures of human trophoblast cells from term placenta were used to further study the expression and regulation of Glut1 and c-fos genes. Fetal calf serum rapidly and transiently (15 to 60 min) stimulated c-fos and Glut1 gene expression suggesting that both genes share similar growth factor-controlled pathways. Glucose inhibited Glut1, but not c-fos expression. An eight-fold decrease in Glut1 mRNA was observed when glucose concentration in the medium was increased from 0 to 25 mM, whereas c-fos mRNA levels remained very low. These results suggest that in the human placenta, the expression of Glut1 is specifically regulated by glucose concentration. These data demonstrate that (1) Glut1 and c-fos mRNA transcripts are expressed in the human placenta exhibiting an age-specific pattern of expression, (2) In cultured trophoblast cells, both genes are stimulatable by fetal calf serum and in contrast to c-fos, Glut1 is negatively regulated by glucose. This differential regulation of Glut1 and c-fos genes could be relevant to specific metabolic and mitogenic pathways implicated in placental growth and differentiation.

摘要

葡萄糖转运蛋白1(Glut1)是脑/红细胞葡萄糖转运体,是人类胎盘的一种主要亚型,其表达呈现年龄特异性模式,孕早期的mRNA水平比足月胎盘高五倍。相比之下,胰岛素可调节的葡萄糖转运蛋白Glut4的mRNA水平在整个孕期都处于检测极限,表明该亚型在胎盘中的表达非常低。核原癌基因c-fos和c-myc在人类胎盘中也可检测到,但c-fos仅呈现年龄特异性表达模式,孕晚期的水平高于足月胎盘。来自足月胎盘的人滋养层细胞原代培养用于进一步研究Glut1和c-fos基因的表达及调控。胎牛血清迅速且短暂地(15至60分钟)刺激c-fos和Glut1基因表达,表明这两个基因共享相似的生长因子控制途径。葡萄糖抑制Glut1的表达,但不抑制c-fos的表达。当培养基中的葡萄糖浓度从0增加到25 mM时,观察到Glut1 mRNA下降了八倍,而c-fos mRNA水平仍然很低。这些结果表明,在人类胎盘中,Glut1的表达受葡萄糖浓度特异性调节。这些数据表明:(1)Glut1和c-fos mRNA转录本在人类胎盘中表达,呈现年龄特异性表达模式;(2)在培养的滋养层细胞中,这两个基因都可被胎牛血清刺激,与c-fos不同,Glut1受葡萄糖负调控。Glut1和c-fos基因的这种差异调节可能与胎盘生长和分化所涉及的特定代谢和有丝分裂途径相关。

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