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首页> 外文期刊>American Journal of Physiology >Studies of mucus in mouse stomach, small intestine, and colon. III. Gastrointestinal Muc5ac and Muc2 mucin O-glycan patterns reveal a regiospecific distribution
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Studies of mucus in mouse stomach, small intestine, and colon. III. Gastrointestinal Muc5ac and Muc2 mucin O-glycan patterns reveal a regiospecific distribution

机译:研究小鼠胃,小肠和结肠中的粘液。三,胃肠道Muc5ac和Muc2黏蛋白O型聚糖显示区域特异性分布

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The mouse intestinal mucus is mainly made up by the gel-forming Muc2 mucin and the stomach surface mucus Muc5ac, both extensively O-glycosylated. The oligosaccharide diversity provides a vast library of potential recognition sites for both commensal and pathogenic organisms. The mucin glycans are thus likely very important for the selection and maintenance of a stable intestinal flora. Here we have explored the O-glycan patterns of the mouse gastrointestinal tract mucins. The mucins from the mucus of the distal and proximal colon, ileum, jejunum, duodenum, and stomach of conventionally raised wild-type (C57BL/6) mice were separated by composite gel electrophoresis. The O-linked glycans were released by reductive elimination and structurally characterized by liquid chromatography-mass spectrometry. The mucins glycans were mostly core 2 type [Galβ1-3(GlcNAcβ1-6)GalNAcol], but also core 1 (Galβ1-3GalNAcol). In the stomach about half of the Muc5ac mucin O-glycans were neutral and many monosulfated, but with a low grade of sialylation and fucosylation. Mouse ileum, jejunum, and duodenum had similar glycan patterns dominated by sialylated and sulfated core 2 glycans, but few fucosylated. Colon was on the other hand dominated by highly charged fucosylated glycans. The distal colon is different from the proximal colon because different biosynthetic pathways are utilized, although sialylated and sulfated glycans were highly abundant in both parts. The sulfation was higher in the distal colon, whereas sialic acid was more common in the proximal colon. Many fucosylated glycans were found in both the proximal and distal colon. Thus the mucin O-glycans vary along the mouse gastrointestinal tract.
机译:小鼠肠粘液主要由形成凝胶的Muc2粘蛋白和胃表面粘液Muc5ac组成,两者都被O-糖基化。寡糖多样性为共生和致病生物提供了巨大的潜在识别位点库。因此,粘蛋白聚糖对于选择和维持稳定的肠道菌群可能非常重要。在这里,我们探索了小鼠胃肠道粘蛋白的O型聚糖模式。通过复合凝胶电泳分离常规饲养的野生型(C57BL / 6)小鼠的远端和近端结肠,回肠,空肠,十二指肠和胃的粘液中的粘蛋白。 O-连接的聚糖通过还原消除而释放,并通过液相色谱-质谱法进行结构表征。粘蛋白聚糖多为核心2型[Galβ1-3(GlcNAcβ1-6)GalNAcol],但也有核心1型(Galβ1-3GalNAcol)。在胃中,大约一半的Muc5ac粘蛋白O聚糖是中性的,许多被单硫酸化,但是唾液酸化和岩藻糖基化程度较低。小鼠回肠,空肠和十二指肠具有类似的聚糖模式,其中唾液酸化和硫酸化的核心2聚糖占优势,但岩藻糖基化很少。另一方面,结肠是由高电荷岩藻糖基化聚糖所主导。远端结肠不同于近端结肠,因为利用了不同的生物合成途径,尽管唾液酸化和硫酸化的聚糖在两个部分中都高度丰富。硫酸化在远端结肠中较高,而唾液酸在远端结肠中更常见。在近端和远端结肠中都发现了许多岩藻糖基化的聚糖。因此,粘蛋白O-聚糖沿小鼠胃肠道变化。

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