Lee Seung Ho, Takahashi Motoko, Honke Koichi, Miyoshi Eiji, Osumi Daisuke, Sakiyama Haruhiko, Ekuni Atsuko, Wang Xiangchun, Inoue Shinya, Gu Jianguo, Kadomatsu Kenji, Taniguchi Naoyuki
Department of Biochemistry, Osaka University Graduate School of Medicine, B1, 2-2 Yamadaoka, Suita, Osaka 565-0871.
J Biochem. 2006 Mar;139(3):391-8. doi: 10.1093/jb/mvj039.
alpha1,6-Fucosyltransferase (Fut8) catalyzes the transfer of a fucose residue from GDP-fucose to the innermost N-acetylglucosamine residue of N-glycans. Here we report that the loss of core fucosylation impairs the function of low-density lipoprotein (LDL) receptor-related protein-1 (LRP-1), a multifunctional scavenger and signaling receptor, resulting in a reduction in the endocytosis of insulin like growth factor (IGF)-binding protein-3 (IGFBP-3) in the cells derived from Fut8-null (Fut8-/-) mice. The reduced endocytosis was restored by the re-introduction of Fut8. Serum levels of IGFBP-3 were markedly upregulated in Fut8-/- mice. These data clearly indicate that core fucosylation is crucial for the scavenging activity of LRP-1 in vivo.
α1,6-岩藻糖基转移酶(Fut8)催化岩藻糖残基从GDP-岩藻糖转移至N-聚糖最内侧的N-乙酰葡糖胺残基上。在此我们报告,核心岩藻糖基化缺失会损害低密度脂蛋白(LDL)受体相关蛋白1(LRP-1)的功能,LRP-1是一种多功能清道夫和信号受体,这会导致来自Fut8基因敲除(Fut8-/-)小鼠的细胞中胰岛素样生长因子(IGF)结合蛋白3(IGFBP-3)的内吞作用减少。通过重新引入Fut8可恢复减少的内吞作用。Fut8-/-小鼠血清中IGFBP-3水平显著上调。这些数据清楚地表明,核心岩藻糖基化对于LRP-1在体内的清道夫活性至关重要。