麦胶蛋白是一种未分类的toll样受体配体

Shirin Moossavi
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引用次数: 5

摘要

乳糜泻是一种慢性肠道炎症,是由遗传易感宿主对小麦家族谷物成分的不适当免疫反应引起的。麦胶蛋白是小麦的主要致病成分;它们的毒性和免疫原性取决于它们的氨基酸序列。他们是已知的启动先天和适应性免疫反应。然而,目前尚不清楚它们是如何被肠上皮细胞和免疫细胞识别的。toll样受体(TLRs)是模式识别受体中研究最多的一类,它通过识别病原体和损伤相关的分子模式,在启动先天免疫中起着关键作用。外源性食物来源的蛋白质尚未被识别为TLR配体。麦胶蛋白在体外可激活TLR信号通路。现有的证据表明麦胶蛋白和/或其他小麦成分直接参与激活TLR信号。然而,目前已有的数据存在争议,主要集中在tlr2和TLR4上。据推测,麦胶蛋白是其中一种tlr的直接配体。如果麦胶蛋白确实被证明是tlr的直接配体,我们对胃肠道疾病,如结直肠癌的发病机制的理解也将受到很大的影响。为了充分认识麦胶蛋白作为直接TLR配体的作用,它应该被证明与一个或多个TLR分子物理相互作用并结合。此外,应该证明TLR通路激活是麦胶蛋白/TLR结合的下游效应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Gliadin is an uncatalogued Toll-like receptor ligand

Coeliac disease is a chronic intestinal inflammatory condition, which is caused by an inappropriate immune response to components of wheat family cereals in a genetically susceptible host. Gliadins are the major pathogenic constituent of wheat; their toxicity and immunogenicity depend on their amino acid sequence. They are known to initiate the innate and the adaptive immune response. Nevertheless, it is not yet known how they are recognised by the intestinal epithelium and immune cells. Toll-like receptors (TLRs) are the best-studied group of pattern recognition receptors, which play a critical role in the initiation of innate immunity through the recognition of pathogen- and damage-associated molecular patterns. Exogenous food-derived proteins are not yet recognised as TLR ligands. Gliadin can activate TLR signalling pathway in vitro. The existing evidence is suggestive of the direct contribution of gliadin and/or other wheat components to activating TLR signalling. However, the data available so far are controversial and are mainly focussed on TLR 2 and TLR4. It is hypothesised that gliadin is a direct ligand for one of the TLRs. If indeed gliadin is proven to be a direct ligand of TLRs, our understanding of the pathogenesis of gastrointestinal diseases, such as colorectal cancer, will also be greatly influenced. In order to fully appreciate the role of gliadin as a direct TLR ligand, it should be proven to interact physically with and bind to one or more of the TLR molecules. Furthermore, it should be documented that TLR pathway activation is the downstream effect of gliadin/TLR binding.

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