Mote P L, Tillman J B, Spindler S R
Department of Biochemistry, University of California, Riverside 92521, USA.
Mech Ageing Dev. 1998 Aug 14;104(2):149-58. doi: 10.1016/s0047-6374(98)00064-5.
The endoplasmic reticulum chaperone glucose-regulated protein 78 (GRP78) is essential for the proper glycosylation, folding and assembly of many membrane bound and secreted proteins. GRP78 mRNA is well known to be induced in cultured cells by lowering medium glucose concentrations from 4.5 to 0 mg/ml. Here we report a study designed to determine the effects of intermediate concentrations of glucose on GRP78 mRNA abundance. Progressive reduction in culture medium glucose from 4.5 to 1.0 mg/ml progressively reduced GRP78 mRNA to approximately 30% of the initial level. Induction of GRP78 mRNA by glucose starvation was observed in medium containing less than 1 mg/ml glucose. Determination of the amount of glucose consumed in these cultures showed that reduction of glucose concentrations led first to repression of GRP78 mRNA abundance, followed by induction of the mRNA only when glucose is nearly exhausted. Caloric restriction in mice both reduces fasting and mean 24 h glucose blood concentrations and GRP78 mRNA abundance in the liver. Thus, it is possible that negative regulation of GRP78 mRNA in the liver is due directly to reduced blood glucose concentrations.
内质网伴侣蛋白葡萄糖调节蛋白78(GRP78)对于许多膜结合蛋白和分泌蛋白的正确糖基化、折叠和组装至关重要。众所周知,在培养细胞中,将培养基葡萄糖浓度从4.5毫克/毫升降至0毫克/毫升可诱导GRP78 mRNA表达。在此,我们报告一项旨在确定中等浓度葡萄糖对GRP78 mRNA丰度影响的研究。将培养基中的葡萄糖从4.5毫克/毫升逐步降至1.0毫克/毫升,可使GRP78 mRNA逐步降至初始水平的约30%。在葡萄糖含量低于1毫克/毫升的培养基中观察到葡萄糖饥饿诱导GRP78 mRNA表达。对这些培养物中葡萄糖消耗量的测定表明,葡萄糖浓度降低首先导致GRP78 mRNA丰度受到抑制,随后仅在葡萄糖几乎耗尽时才诱导mRNA表达。小鼠的热量限制既能降低空腹血糖和24小时平均血糖浓度,也能降低肝脏中GRP78 mRNA的丰度。因此,肝脏中GRP78 mRNA的负调控可能直接归因于血糖浓度降低。