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人胎盘葡萄糖转运蛋白表达及活性的血糖调节

Glycaemic regulation of glucose transporter expression and activity in the human placenta.

作者信息

Illsley N P, Sellers M C, Wright R L

机构信息

Department of Obstetrics and Gynecology, UMDNJ-New Jersey Medical School, Newark 07103-2714, USA.

出版信息

Placenta. 1998 Sep;19(7):517-24. doi: 10.1016/s0143-4004(98)91045-1.

Abstract

To determine whether the expression and activity of glucose transporters in human trophoblast are regulated by glucose, syncytiotrophoblast cells, choriocarcinoma cells, and villous fragments were incubated with a range of glucose concentrations (0-20 mM, 24 h). Expression of GLUT1 and GLUT3 glucose transporters was measured by immunoblotting, while glucose transporter activity was determined by [3H]2-deoxyglucose uptake in the cultured cells. GLUT1 expression in syncytial cells was enhanced following incubation in absence of glucose, reduced by incubation in 20 mM glucose but was not altered by incubation at 1 or 12 mM glucose. Transporter activity was inversely related to extracellular glucose over the entire range of concentrations tested (0-20 mM). Incubation of villous fragments in 20 mM glucose produced a limited suppression of GLUT1 expression, but no effects were noted following incubation at 0 or 1 mM glucose. Neither GLUT1 expression in JAr and JEG-3 choriocarcinoma cells nor transport activity in JEG-3 cells was affected by extracellular glucose concentration. Unlike syncytial cells, JAr, JEG-3 and BeWo all expressed GLUT3 protein in addition to GLUT1. These results show that while syncytiotrophoblast GLUT1 expression is altered at the extremes of extracellular glucose concentration, it is refractory to glucose alone at lower concentrations. By contrast, an inverse relationship exists between glucose transporter activity and extracellular glucose. This suggests that there are post-translational regulatory mechanisms which may respond to changes in extracellular glucose concentration.

摘要

为了确定人滋养层细胞中葡萄糖转运蛋白的表达和活性是否受葡萄糖调节,将合体滋养层细胞、绒毛膜癌细胞和绒毛片段与一系列葡萄糖浓度(0 - 20 mM,24小时)一起孵育。通过免疫印迹法检测GLUT1和GLUT3葡萄糖转运蛋白的表达,而葡萄糖转运蛋白活性则通过培养细胞中[3H]2 - 脱氧葡萄糖摄取来测定。在无糖条件下孵育后,合体细胞中GLUT1的表达增强,在20 mM葡萄糖中孵育会使其降低,但在1 mM或12 mM葡萄糖中孵育则无变化。在测试的整个浓度范围内(0 - 20 mM),转运蛋白活性与细胞外葡萄糖呈负相关。将绒毛片段在20 mM葡萄糖中孵育会对GLUT1表达产生有限的抑制,但在0 mM或1 mM葡萄糖中孵育后未观察到影响。JAr和JEG - 3绒毛膜癌细胞中的GLUT1表达以及JEG - 3细胞中的转运活性均不受细胞外葡萄糖浓度的影响。与合体细胞不同,JAr、JEG - 3和BeWo除了表达GLUT1外,还表达GLUT3蛋白。这些结果表明,虽然合体滋养层GLUT1的表达在细胞外葡萄糖浓度的极端情况下会发生改变,但在较低浓度下对单独的葡萄糖不敏感。相比之下,葡萄糖转运蛋白活性与细胞外葡萄糖之间存在负相关。这表明存在可能对细胞外葡萄糖浓度变化作出反应的翻译后调节机制。

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