Department of Disease Glycomics, Institute of Scientific and Industrial Research, Osaka University, 8-1 Mihogaoka, Ibaraki, Osaka 567-0047, Japan.
J Clin Biochem Nutr. 2011 Jan;48(1):20-5. doi: 10.3164/jcbn.11-015FR. Epub 2010 Dec 29.
Glucose is an energy substrate, as well as the primary source of nucleotide sugars, which are utilized as donor substrates in protein glycosylation. Appropriate glycosylation is necessary to maintain the stability of protein, and is also important in the localization and trafficking of proteins. The dysregulation of glycosylation results in the development of a variety of disorders, such as cancer, diabetes mellitus and emphysema. Glycosylation is kinetically regulated by dynamically changing the portfolio of glycosyltransferases, nucleotide sugars, and nucleotide sugar transporters, which together form a part of what is currently referred to as the "Glycan cycle". An excess or a deficiency in the expression of glycosyltransferases has been shown to alter the glycosylation pattern, which subsequently leads to the onset, progression and exacerbation of a number of diseases. Furthermore, alterations in intracellular nucleotide sugar levels can also modulate glycosylation patterns. It is observed that pathological hypoxic microenvironments frequently occur in solid cancers and inflammatory foci. Hypoxic conditions dramatically change gene expression profiles, by activating hypoxia-inducible factor-1, which mediates adaptive cellular responses. Hypoxia-induced glycosyltransferases and nucleotide sugar transporters have been shown to modulate glycosylation patterns that are part of the mechanism associated with cancer metastasis. Hypoxia-inducible factor-1 also induces the expression of glucose transporters and various types of glycolytic enzymes, leading to shifts in glucose metabolic patterns. This fact strongly suggests that hypoxic conditions are an important factor in modulating various nucleotide sugar biosynthetic pathways. This review discusses some of the current thinking of how hypoxia alters glucose metabolic fluxes that can modulate cellular glycosylation patterns and consequently modify cellular functions, particularly from the standpoint of the N-acetylglucosamine cycle, a part of the "Glycan cycle".
葡萄糖是一种能量底物,也是核苷酸糖的主要来源,核苷酸糖可用作蛋白质糖基化的供体底物。适当的糖基化对于维持蛋白质的稳定性是必要的,对于蛋白质的定位和运输也是重要的。糖基化的失调导致了多种疾病的发展,如癌症、糖尿病和肺气肿。糖基化通过动态改变糖基转移酶、核苷酸糖和核苷酸糖转运蛋白的组合来进行动力学调节,这些共同构成了当前所谓的“聚糖循环”的一部分。糖基转移酶的表达过多或不足已被证明会改变糖基化模式,从而导致许多疾病的发生、发展和恶化。此外,细胞内核苷酸糖水平的改变也可以调节糖基化模式。人们观察到,在实体瘤和炎症灶中经常出现病理性低氧微环境。缺氧条件通过激活缺氧诱导因子-1,显著改变基因表达谱,从而介导适应性细胞反应。已经表明,缺氧诱导的糖基转移酶和核苷酸糖转运蛋白可以调节糖基化模式,这是与癌症转移相关的机制的一部分。缺氧诱导因子-1还诱导葡萄糖转运蛋白和各种类型的糖酵解酶的表达,导致葡萄糖代谢模式的转变。这一事实强烈表明,缺氧条件是调节各种核苷酸糖生物合成途径的重要因素。本文综述了一些关于缺氧如何改变葡萄糖代谢通量的现有观点,这些改变可以调节细胞糖基化模式,并进而改变细胞功能,特别是从 N-乙酰葡萄糖胺循环的角度来看,这是“聚糖循环”的一部分。