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葡萄糖进入大鼠系膜细胞是由钠耦联转运体和易化转运体介导的。

Glucose entry into rat mesangial cells is mediated by both Na(+)-coupled and facilitative transporters.

作者信息

Wakisaka M, He Q, Spiro M J, Spiro R G

机构信息

Department of Biological Chemistry, Harvard Medical School, Boston, Massachusetts, USA.

出版信息

Diabetologia. 1995 Mar;38(3):291-7. doi: 10.1007/BF00400633.

Abstract

Since previous studies from our laboratory have demonstrated that increased glucose consumption by cultured rat mesangial cells is accompanied by an accelerated production of type IV and type VI collagen, we have now examined the manner by which glucose is transported into these cells. A progressive stimulation of glucose uptake by the mesangial cells was observed with increasing concentrations of NaCl so that at 145 mmol/l about twice as much glucose entered the cells as in its absence (substituted by choline chloride). Moreover, since phlorizin inhibited the NaCl-promoted uptake of glucose and this salt was found to increase the accumulation of alpha-methylglucoside in a manner which could not be duplicated by KCl or mannitol, both Na(+)-coupled and facilitative glucose transporters appeared to be present in the cells. Km values of 1.93 mmol/l and 1.36 mmol/l were determined for the co-transport and facilitated transport pathways, respectively, with their Vmax being 29.5 and 18.0 nmol.mg protein-1.h-1. Both uptake activities were found to be down-regulated by exposure of the cells to high glucose and furthermore the Na(+)-dependent transport could no longer be detected after about 12 passages of the cells. Hybridization of mesangial cell mRNA with cDNA probes revealed transcripts for the Na+/glucose co-transporter as well as GLUT1 and to a lesser extent GLUT4.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

由于我们实验室之前的研究表明,培养的大鼠系膜细胞葡萄糖消耗增加伴随着IV型和VI型胶原蛋白生成加速,我们现在研究了葡萄糖进入这些细胞的方式。随着NaCl浓度升高,观察到系膜细胞对葡萄糖摄取呈渐进性刺激,以至于在145 mmol/l时进入细胞的葡萄糖量约为无NaCl(用氯化胆碱替代)时的两倍。此外,由于根皮苷抑制了NaCl促进的葡萄糖摄取,且发现这种盐以一种KCl或甘露醇无法复制的方式增加了α-甲基葡萄糖苷的积累,细胞中似乎同时存在Na⁺偶联型和易化型葡萄糖转运体。共转运和易化转运途径的Km值分别测定为1.93 mmol/l和1.36 mmol/l,其Vmax分别为29.5和18.0 nmol·mg蛋白⁻¹·h⁻¹。发现将细胞暴露于高糖环境会下调两种摄取活性,而且在细胞传代约12次后,Na⁺依赖性转运就无法再检测到了。系膜细胞mRNA与cDNA探针杂交显示有Na⁺/葡萄糖共转运体以及GLUT1的转录本,GLUT4的转录本较少。(摘要截短于250字)

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