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GLUT 3在克隆大鼠骨肉瘤细胞系UMR 106-01中的表达及胰岛素对其的调控

Expression and regulation by insulin of GLUT 3 in UMR 106-01, a clonal rat osteosarcoma cell line.

作者信息

Thomas D M, Maher F, Rogers S D, Best J D

机构信息

University of Melbourne Department of Medicine, St Vincents Hospital, Fitzroy, Victoria, Australia.

出版信息

Biochem Biophys Res Commun. 1996 Jan 26;218(3):789-93. doi: 10.1006/bbrc.1996.0140.

Abstract

Expression of the glucose transporter GLUT 3 is mainly restricted to neuronal tissues, with lower levels in testis and placenta. In addition, GLUT 3 has recently been reported in neonatal rat calvaria by in situ hybridisation. We report the co-expression of GLUT 1 and GLUT 3 mRNA and protein in UMR 106-01, a clonal osteosarcoma cell line. By semi-quantitative analysis we show that GLUT 3 protein is expressed at levels comparable to GLUT 1. Insulin stimulates glucose uptake in UMR 106-01 cells. GLUT 3 mRNA and protein are increased by chronic (16 h) treatment with insulin, and the increase in GLUT 3 mRNA is not inhibited by cycloheximide. Regulation of GLUT 3 mRNA by insulin has not been previously shown. UMR 106-01 represents a useful model for investigating regulation of GLUT 3 expression.

摘要

葡萄糖转运蛋白GLUT 3的表达主要局限于神经组织,在睾丸和胎盘中水平较低。此外,最近通过原位杂交在新生大鼠颅骨中发现了GLUT 3。我们报告了在克隆性骨肉瘤细胞系UMR 106 - 01中GLUT 1和GLUT 3 mRNA及蛋白的共表达。通过半定量分析我们发现,GLUT 3蛋白的表达水平与GLUT 1相当。胰岛素可刺激UMR 106 - 01细胞摄取葡萄糖。长期(16小时)胰岛素处理可使GLUT 3 mRNA和蛋白增加,且GLUT 3 mRNA的增加不受放线菌酮抑制。胰岛素对GLUT 3 mRNA的调控此前尚未见报道。UMR 106 - 01是研究GLUT 3表达调控的有用模型。

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