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大鼠胰岛β细胞和α细胞发育过程中葡萄糖激酶的表达与调控

Expression and regulation of glucokinase in rat islet beta- and alpha-cells during development.

作者信息

Tu J, Tuch B E, Si Z

机构信息

Pancreas Transplant Unit, The Prince of Wales Hospital, Faculty of Medicine, The University of New South Wales, Sydney, Australia.

出版信息

Endocrinology. 1999 Aug;140(8):3762-6. doi: 10.1210/endo.140.8.6879.

Abstract

Glucokinase (GK) is the rate-limiting enzyme in the glycolytic pathway of the beta-cell and, even in the rat fetus at 22-days gestation, immediately before birth, acts as a sensor of glucose influencing the rate of glucose utilization. However, when GK first appears in islets during beta-cell development is unknown. Whether GK is expressed in fetal glucagon-producing cells is also unknown. To determine this information, fetal rat islets were examined at 16-, 18-, and 22-days gestation. GK was identified immunocytochemically in both beta- and alpha-cells at all these ages, with the number of GK immunoreactive cells positively correlated to the fetal age from 16-22 days. Western blot analysis of islet protein extracts demonstrated the presence of GK, at 52 kDa, at 16 days and thereafter. To determine whether glucose had any effect on regulation of GK biosynthesis, fetal islets were cultured in medium containing a wide range of concentrations of glucose for 7 days. The amount of GK protein was significantly decreased in low concentrations of glucose and augmented at high concentrations. In conclusion, GK was expressed in both beta- and alpha-cells in fetal rat islets during development. GK is an integral part of the function of both of these cells at all stages in the development of the fetal islet.

摘要

葡萄糖激酶(GK)是β细胞糖酵解途径中的限速酶,即使在妊娠22天的大鼠胎儿中,即在出生前,它也作为葡萄糖传感器影响葡萄糖利用速率。然而,GK在β细胞发育过程中首次出现在胰岛的时间尚不清楚。GK是否在胎儿产生胰高血糖素的细胞中表达也不清楚。为了确定这些信息,对妊娠16、18和22天的大鼠胎儿胰岛进行了检查。在所有这些年龄段的β细胞和α细胞中均通过免疫细胞化学方法鉴定出了GK,从16天到22天,GK免疫反应性细胞的数量与胎龄呈正相关。对胰岛蛋白提取物进行的蛋白质印迹分析表明,在16天及之后均存在52 kDa的GK。为了确定葡萄糖对GK生物合成的调节是否有任何影响,将胎儿胰岛在含有多种葡萄糖浓度的培养基中培养7天。低浓度葡萄糖时GK蛋白量显著减少,高浓度时增加。总之,在发育过程中,GK在大鼠胎儿胰岛的β细胞和α细胞中均有表达。在胎儿胰岛发育的所有阶段,GK都是这两种细胞功能不可或缺的一部分。

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