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小鼠LM细胞中寡糖-脂质合成与蛋白质合成之间的关系。

Relationship between oligosaccharide-lipid synthesis and protein synthesis in mouse LM cells.

作者信息

Grant S R, Lennarz W J

出版信息

Eur J Biochem. 1983 Aug 15;134(3):575-83. doi: 10.1111/j.1432-1033.1983.tb07605.x.

Abstract

Previous studies from several laboratories have reported that inhibition of protein synthesis results in a concomitant reduction in synthesis of oligosaccharide-diphosphoryldolichol. We have investigated this phenomenon in LM cells grown in defined culture medium. The results of this study indicate that incubation of LM cell with cycloheximide at a concentration sufficient to totally arrest polypeptide synthesis, results in a rapid reduction in the synthesis of [3H]mannose-labeled or [3H]glucosamine-labeled oligosaccharide-lipid within 2 min. Cycloheximide treatment had only a slight inhibitory effect on synthesis of GDP-Man. Furthermore, during the first 5 min after the addition of cycloheximide to LM cells, when [3H]mannose incorporation into oligosaccharide-lipid was maximally reduced, the specific activity of the GDP-Man pool was identical to that observed in control cells. Labeling in vivo of the lipid-linked saccharide precursors of oligosaccharide-lipid revealed that cycloheximide had virtually no effect on the synthesis of Man-P-Dol, GlcNAc-PP-Dol, GlcNAc2-PP-Dol, and beta-Man-(GlcNAc)2-PP-Dol (Dol = dolichol). In agreement with this finding, results of experiments in vitro using microsomes prepared from LM cells indicate that cycloheximide did not directly inhibit the enzymes responsible for the synthesis of these lipid-linked saccharide precursors. Supplementation of mouse LM cells by preincubation for 1 h with dolichyl phosphate (5 micrograms/ml) resulted in a 300% stimulation of oligosaccharide-lipid synthesis when compared to non-supplemented cells. However, dolichyl phosphate supplementation of cycloheximide-treated cells failed to restore oligosaccharide-lipid synthesis to the level observed in control cells. In control cells pre-labeled oligosaccharide-lipid turned over rapidly and, as expected, cycloheximide addition to the chase medium significantly retarded this turnover process. However, preincubation of cells with exogenous dolichyl phosphate had little or no effect on the turnover of oligosaccharide-lipid in control or cycloheximide-treated cells. These findings argue against dolichyl phosphate deficiency as the primary cause of reduced oligosaccharide-lipid synthesis when protein synthesis is blocked. The implications of these results, and an alternative hypothesis to explain the effect of inhibition of protein synthesis on oligosaccharide-lipid synthesis based on elevation of intracellular GTP levels, are discussed.

摘要

几个实验室之前的研究报告称,蛋白质合成的抑制会导致寡糖 - 二磷酸多萜醇的合成随之减少。我们在限定培养基中培养的LM细胞中研究了这一现象。本研究结果表明,用足以完全阻止多肽合成的浓度的环己酰亚胺孵育LM细胞,会在2分钟内导致[3H]甘露糖标记或[3H]葡糖胺标记的寡糖 - 脂质的合成迅速减少。环己酰亚胺处理对GDP - Man的合成只有轻微的抑制作用。此外,在向LM细胞添加环己酰亚胺后的最初5分钟内,当[3H]甘露糖掺入寡糖 - 脂质的量最大程度减少时,GDP - Man池的比活性与对照细胞中观察到的相同。对寡糖 - 脂质的脂质连接糖前体进行体内标记显示,环己酰亚胺实际上对Man - P - Dol、GlcNAc - PP - Dol、GlcNAc2 - PP - Dol和β - Man - (GlcNAc)2 - PP - Dol(Dol = 多萜醇)的合成没有影响。与此发现一致,使用从LM细胞制备的微粒体进行的体外实验结果表明,环己酰亚胺不会直接抑制负责这些脂质连接糖前体合成的酶。与未补充的细胞相比,用磷酸多萜醇(5微克/毫升)预孵育1小时对小鼠LM细胞进行补充,导致寡糖 - 脂质合成增加了300%。然而,用磷酸多萜醇补充经环己酰亚胺处理的细胞未能将寡糖 - 脂质合成恢复到对照细胞中观察到的水平。在对照细胞中,预先标记的寡糖 - 脂质周转迅速,正如预期的那样,向追踪培养基中添加环己酰亚胺显著延缓了这一周转过程。然而,用外源性磷酸多萜醇对细胞进行预孵育对对照或经环己酰亚胺处理的细胞中寡糖 - 脂质的周转几乎没有影响。这些发现反对将磷酸多萜醇缺乏作为蛋白质合成受阻时寡糖 - 脂质合成减少的主要原因。讨论了这些结果的意义,以及基于细胞内GTP水平升高来解释蛋白质合成抑制对寡糖 - 脂质合成影响的另一种假设。

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