首页> 外文期刊>Journal of Biochemistry >Loss of Core Fucosylation of Low-Density Lipoprotein Receptor–Related Protein-1 Impairs Its Function, Leading to the Upregulation of Serum Levels of Insulin-Like Growth Factor–Binding Protein 3 in Fut8?/? Mice
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Loss of Core Fucosylation of Low-Density Lipoprotein Receptor–Related Protein-1 Impairs Its Function, Leading to the Upregulation of Serum Levels of Insulin-Like Growth Factor–Binding Protein 3 in Fut8?/? Mice

机译:低密度脂蛋白受体相关蛋白-1的核心岩藻糖基化丧失会损害其功能,导致Fut8 ?/?小鼠血清胰岛素样生长因子结合蛋白3的血清水平上调

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摘要

α1,6-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.
机译:α1,6-岩藻糖基转移酶(Fut8)催化将岩藻糖残基从GDP岩藻糖转移至N-聚糖的最内层N-乙酰基氨基葡萄糖残基。在这里,我们报道核心岩藻糖基化的丧失削弱了低密度脂蛋白(LDL)受体相关蛋白1(LRP-1)(一种多功能清除剂和信号受体)的功能,导致胰岛素样生长的内吞作用减少Fut8无效(Fut8 -/-)小鼠细胞中的IGF(IGF)结合蛋白3(IGFBP-3)。通过重新引入Fut8恢复了减少的内吞作用。在Fut8 -/-小鼠中,IGFBP-3的血清水平显着上调。这些数据清楚地表明核心岩藻糖基化对于体内LRP-1的清除活性至关重要。

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