首页> 美国卫生研究院文献>Infection and Immunity >Sialo-oligosaccharide receptors for Mycoplasma pneumoniae and related oligosaccharides of poly-N-acetyllactosamine series are polarized at the cilia and apical-microvillar domains of the ciliated cells in human bronchial epithelium.
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Sialo-oligosaccharide receptors for Mycoplasma pneumoniae and related oligosaccharides of poly-N-acetyllactosamine series are polarized at the cilia and apical-microvillar domains of the ciliated cells in human bronchial epithelium.

机译:肺炎支原体的唾液寡糖受体和聚-N-乙酰基乳糖胺系列的相关寡糖在人支气管上皮的纤毛细胞的纤毛和顶端-微绒毛区极化。

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摘要

The occurrence and distribution of the sialo-oligosaccharide receptors (sialosyl-I and sialosyl-i) for Mycoplasma pneumoniae as well as other related oligosaccharide structures of poly-N-acetyllactosamine type, and their short-chain analogs based on galactose linked beta 1-4 or beta 1-3 to N-acetylglucosamine (Gal beta 1-4GlcNAc or Gal beta 1-3GlcNAc, respectively) were investigated in the human bronchial epithelium by histochemistry by using sequence-specific monoclonal antibodies and lectins. Among the mature epithelial cells, only ciliated cells were found to express the long-chain antigens, whereas mucus-secreting cells contained the short-chain antigens associated with mucus globules. The long-chain oligosaccharides were found to be highly polarized at the luminal aspects of the ciliated cells where the branched structures (I and sialosyl-I antigens) were detected both at the apical-microvillar border and on the cilia, but the linear structures (i, sialosyl-i, and VIM-2 antigens) were detected exclusively at the apical-microvillar border. These observations provide the first in situ visualization of the receptor structures for M. pneumoniae at the primary site of infection. The lack of sialo-oligosaccharide receptors in secretory cells and the mucus they produce provides a biochemical basis for evasion by this microorganism of the secreted mucus barrier.
机译:肺炎支原体的唾液寡糖受体(唾液酰基-I和唾液酰基-i)以及其他相关的聚-N-乙酰基乳糖胺型寡糖结构及其基于半乳糖连接的β1-的短链类似物的发生和分布使用序列特异性单克隆抗体和凝集素通过组织化学方法在人支气管上皮中研究了N-乙酰氨基葡萄糖的4或β1-3(分别为Gal 1 1-4GlcNAc或Gal beta 1-3GlcNAc)。在成熟的上皮细胞中,仅纤毛细胞表达长链抗原,而分泌粘液的细胞含有与粘液小球相关的短链抗原。发现长链寡糖在纤毛细胞的管腔方面高度极化,在那里在顶端-微绒毛边缘和纤毛上都检测到分支结构(I和唾液酰-I抗原),但是线性结构( i,唾液酰基-i和VIM-2抗原)仅在根尖-微绒毛边界处检测到。这些观察提供了肺炎支原体在感染的主要部位的受体结构的第一现场观察。分泌细胞及其产生的粘液中缺少唾液寡糖受体,为该微生物逃避分泌的粘液屏障提供了生化基础。

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