首页> 美国卫生研究院文献>Clinical Molecular Pathology >Abnormal fucosylation of-ileal mucus in cystic fibrosis: II. A histochemical study using monoclonal antibodies to fucosyl oligosaccharides.
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Abnormal fucosylation of-ileal mucus in cystic fibrosis: II. A histochemical study using monoclonal antibodies to fucosyl oligosaccharides.

机译:回肠粘液在囊性纤维化中的岩藻糖基化异常:II。使用针对岩藻糖基寡糖的单克隆抗体进行的组织化学研究。

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摘要

Abnormal fucosylation of cystic fibrosis mucin was previously shown using peroxidase conjugated lectins on ileal tissue sections. These abnormally fucosylated glycoproteins were investigated further using monoclonal antibodies to fucosyl oligosaccharides based on type 1 and type 2 blood group precursor chains. The results of this study, using monoclonal antibodies to blood group glycoproteins in cystic fibrosis, were negative, yet abnormal fucosylation had been found using lectin histochemistry. Using monoclonal antibodies, lectins, and appropriate enzymes, such as glycosyl hydrolases, it should be possible to delineate further the abnormality found in glycoproteins in cystic fibrosis on appropriately fixed ileal sections, obtained from infants at term presenting with meconium ileus.
机译:先前已在回肠组织切片上使用过氧化物酶结合的凝集素显示了囊性纤维化粘蛋白的岩藻糖基化异常。使用基于岩藻糖基寡糖的单克隆抗体(基于1型和2型血型前体链)进一步研究了这些异常岩藻糖基化的糖蛋白。使用针对囊性纤维化血型糖蛋白的单克隆抗体的这项研究结果为阴性,但使用凝集素组织化学发现了岩藻糖基化异常。使用单克隆抗体,凝集素和适当的酶(例如糖基水解酶),应该有可能进一步描述在适当固定的回肠切片上发现的囊性纤维化的糖蛋白异常,该回肠切片是从足月肠梗阻患儿获得的。

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