Haspel H C, Wilk E W, Birnbaum M J, Cushman S W, Rosen O M
J Biol Chem. 1986 May 25;261(15):6778-89.
The effect of Glc deprivation (starvation) on hexose transporter (GT) polypeptide(s) (pp) was studied in 3T3-C2 murine fibroblasts. Cells deprived of Glc exhibit 5-fold increases in hexose transport and Glc-displaceable cytochalasin B binding. Immunoblots of membranes reveal a Mr 55,000 GT pp in fed (4 g of Glc/liter) cells and Mr 55,000 and Mr 42,000 GT pp in starved cells. A 10-40-fold increase in total GT pp occurs upon Glc deprivation; part of this accumulation (2-5-fold) is in the Mr 55,000 GT pp, and the remaining increase is in the Mr 42,000 GT pp. During the first 12 h of Glc deprivation only the Mr 55,000 GT pp accumulates. At later times (24-72 h) the Mr 42,000 GT pp appears and constitutes a larger fraction of the total accumulation. Similarly, the Glc concentration dependence of these phenomena reveals that the Mr 55,000 GT pp accumulates at higher concentrations of Glc (less than or equal to g/liter) than the Mr 42,000 GT pp (less than or equal to 0.5 g/liter). Using alternative nutrients, sugar analogs, and inhibitors we observed that the accumulation of total GT pp is dependent upon both hexose phosphate metabolism and the interaction of substrate with the GT. The role(s) of oligosaccharide biosynthesis, protein synthesis, and the transport process itself in the Glc deprivation-induced accumulation of GT pp were examined. The appearance of the Mr 42,000 GT pp but not the Mr 55,000 GT pp was dependent upon protein synthesis. The Glc deprivation-induced accumulation of GT pp is reversible upon refeeding with Glc (4 g/liter, 12 h). This reversal was dependent upon protein synthesis. The electrophoretic mobility of the Mr 42,000 GT pp is similar to the GT pp observed after tunicamycin treatment. The Mr 55,000 but not the Mr 42,000 GT pp binds specifically to agarose-bound wheat germ agglutinin and is sensitive to endoglycosidase F digestion. Oligosaccharide-stripped GT pp and the Mr 42,000 GT pp have the same Mr. The results suggest that the accumulation of total GT pp induced by Glc deprivation is partially independent of the effect of Glc deprivation on glycoprotein biogenesis. The appearance of the Mr 42,000 GT pp with aglyco characteristics is the result of the latter. The accumulation of total GT pp, however, is the result of a specialized and sensitive adaptation of the cell to Glc deprivation. The GT pp synthesized during chronic Glc deprivation has an Mr of 42,000; fed cells synthesize the Mr 55,000 GT pp. Neither the level of in vitro translatable GT mRNA nor the rate of GT pp synthesis are increased by Glc deprivation.(ABSTRACT TRUNCATED AT 400 WORDS)
在3T3 - C2小鼠成纤维细胞中研究了葡萄糖剥夺(饥饿)对己糖转运蛋白(GT)多肽(pp)的影响。缺乏葡萄糖的细胞己糖转运增加5倍,且葡萄糖可置换的细胞松弛素B结合增加。膜的免疫印迹显示,在培养于含4 g葡萄糖/升培养基中的细胞中有一条分子量为55,000的GT pp,而在饥饿细胞中有分子量为55,000和42,000的GT pp。葡萄糖剥夺后总GT pp增加10 - 40倍;这种积累的一部分(2 - 5倍)是分子量为55,000的GT pp,其余的增加是分子量为42,000的GT pp。在葡萄糖剥夺的最初12小时内,只有分子量为55,000的GT pp积累。在后期(24 - 72小时),分子量为42,000的GT pp出现并在总积累中占更大比例。同样,这些现象对葡萄糖浓度的依赖性表明,分子量为55,000的GT pp在较高葡萄糖浓度(≤1 g/升)下积累,而分子量为42,000的GT pp在较低葡萄糖浓度(≤0.5 g/升)下积累。使用替代营养物、糖类类似物和抑制剂,我们观察到总GT pp的积累既依赖于磷酸己糖代谢,也依赖于底物与GT的相互作用。研究了寡糖生物合成、蛋白质合成以及转运过程本身在葡萄糖剥夺诱导的GT pp积累中的作用。分子量为42,000的GT pp而非分子量为55,000的GT pp的出现依赖于蛋白质合成。葡萄糖剥夺诱导的GT pp积累在用4 g/升葡萄糖再喂养12小时后是可逆的。这种逆转依赖于蛋白质合成。分子量为42,000的GT pp的电泳迁移率与衣霉素处理后观察到的GT pp相似。分子量为55,000而非分子量为42,000的GT pp特异性结合琼脂糖结合的麦胚凝集素,且对内切糖苷酶F消化敏感。去除寡糖的GT pp与分子量为42,000的GT pp具有相同分子量。结果表明,葡萄糖剥夺诱导的总GT pp积累部分独立于葡萄糖剥夺对糖蛋白生物合成的影响。具有无糖基特征的分子量为42,000的GT pp的出现是后者的结果。然而,总GT pp的积累是细胞对葡萄糖剥夺的一种特殊且敏感的适应性结果。慢性葡萄糖剥夺期间合成的GT pp分子量为42,000;培养于含葡萄糖培养基中的细胞合成分子量为55,000的GT pp。葡萄糖剥夺既不增加体外可翻译的GT mRNA水平,也不增加GT pp的合成速率。(摘要截断于400字)