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Sialomucin complex in the rat respiratory tract: a model for its role in epithelial protection.

机译:大鼠呼吸道中的唾液粘蛋白​​复合物:其在上皮保护中作用的模型。

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摘要

The pulmonary epithelium has a multitude of specialized functions, which depend on regulated growth and differentiation of several cell types. One such function is the synthesis and secretion of mucins, which offer the epithelium protection from and a means for removal of noxious environmental factors. Sialomucin complex (SMC) is a heterodimeric glycoprotein consisting of a mucin subunit (ASGP-1, ascites sialoglycoprotein-1) and a transmembrane protein (ASGP-2) with two epidermal-growth-factor-like domains. SMC was originally discovered in a highly metastatic rat mammary adenocarcinoma and has been implicated in metastasis and in the protection of the tumour cells from natural killer cells. It can also act as a ligand for the receptor tyrosine kinase 185(neu), suggesting that it is bifunctional as well as heterodimeric. SMC is expressed on the epithelium of rat conducting airways, with the highest levels occurring in the proximal trachea and progressively decreasing into the bronchioles. Airway SMC consists of two forms: a soluble form that lacks the C-terminal cytoplasmic and transmembrane domains and accounts for about 70% of the total, and a membrane-associated form that has the C-terminal domains. Immunocytochemical analyses show that SMC is predominantly present on the apical surfaces of the airway epithelium, but not in goblet cells. Soluble form can be removed from the trachea by rinsing, suggesting that a fraction of the protein is adsorbed to the apical surface. Based on these results, we propose a protective mechanism in which membrane and soluble forms of SMC are produced by airway luminal epithelial cells to provide a cell-associated epithelial glycoprotein barrier that also serves as an interface with flowing mucus. In support of this mechanism, we demonstrated secretion of soluble SMC by primary cultures of tracheal epithelial cells. This model suggests that SMC is a critical element in the protective barrier of the airway epithelium.
机译:肺上皮具有多种特殊功能,这取决于几种细胞类型的调节生长和分化。一种这样的功能是粘蛋白的合成和分泌,其提供上皮保护免受粘液的侵害,并且是一种去除有害环境因子的手段。唾液粘蛋白​​复合物(SMC)是一种异二聚体糖蛋白,由粘蛋白亚基(ASGP-1,腹水唾液酸糖蛋白-1)和跨膜蛋白(ASGP-2)组成,具有两个表皮生长因子样结构域。 SMC最初是在高度转移的大鼠乳腺腺癌中发现的,并与肿瘤的转移以及肿瘤细胞免受自然杀伤细胞的侵害有关。它也可以作为受体酪氨酸激酶185(neu)的配体,表明它是双功能的,也是异二聚的。 SMC在大鼠导气管的上皮中表达,最高水平发生在气管近端,并逐渐降低到细支气管中。气道SMC由两种形式组成:一种缺乏C末端胞质和跨膜结构域的可溶性形式,约占总数的70%;一种具有C末端结构域的膜相关形式。免疫细胞化学分析表明,SMC主要存在于气道上皮的顶表面,而不存在于杯状细胞中。可以通过冲洗将可溶性形式从气管中去除,这表明一部分蛋白质被吸附到根尖表面。基于这些结果,我们提出了一种保护机制,其中气道腔上皮细胞产生SMC的膜和可溶性形式,以提供与细胞相关的上皮糖蛋白屏障,该屏障还充当与流动粘液的界面。为支持该机制,我们证明了气管上皮细胞原代培养物分泌可溶性SMC。该模型表明SMC是气道上皮保护屏障中的关键元素。

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