Habuchi Hiroko, Habuchi Osami, Kimata Koji
Institute for Molecular Science of Medicine, Aichi Medical University, Nagakute, Aichi 480-1195, Japan.
Glycoconj J. 2004;21(1-2):47-52. doi: 10.1023/B:GLYC.0000043747.87325.5e.
Heparan sulfate chains (HS) are initially synthesized on core proteins as linear polysaccharides composed of glucuronic acid--N-acetylglucosamine repeating units and subjected to marked structural modification by sulfation (N-, 2-O-, 6-O-, 3-O-sulfotransferases) and epimerization (C5-epimerase) at the Golgi lumen and further by desulfation (6-O- endosulfatase) at the cell surface, after which divergent fine structures are generated. The expression patterns and specificity of the modifying enzymes are, at least partly, responsible for the elaboration of these fine structures of heparan sulfate. HS interacts with many proteins including growth factors (GF) and morphogens through specific fine structures. Recent biochemical and genetic studies have presented evidence that HS plays important roles in cell behavior and organogenesis. In knock-down experiments of heparan sulfate 6-O-sulfotransferase, 6-O-sulfated units in HS have been shown to act as a stimulator or suppressor according to individual GF/morphogen signaling systems.
硫酸乙酰肝素链(HS)最初在核心蛋白上作为由葡萄糖醛酸 - N - 乙酰葡糖胺重复单元组成的线性多糖合成,并在高尔基体腔中通过硫酸化(N -、2 - O -、6 - O -、3 - O - 磺基转移酶)和差向异构化(C5 - 差向异构酶)进行显著的结构修饰,之后在细胞表面进一步通过脱硫(6 - O - 内切硫酸酯酶)修饰,从而产生不同的精细结构。修饰酶的表达模式和特异性至少部分地决定了硫酸乙酰肝素这些精细结构的形成。HS通过特定的精细结构与包括生长因子(GF)和形态发生素在内的许多蛋白质相互作用。最近的生化和遗传学研究表明,HS在细胞行为和器官发生中起重要作用。在硫酸乙酰肝素6 - O - 磺基转移酶的敲低实验中,HS中的6 - O - 硫酸化单元已被证明根据个体GF/形态发生素信号系统可作为刺激物或抑制剂。