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核苷酸结合寡聚化结构域样受体在黏膜固有免疫和慢性肠道炎症中的双重作用。

The dual role of nod-like receptors in mucosal innate immunity and chronic intestinal inflammation.

作者信息

Corridoni Daniele, Arseneau Kristen O, Cifone Maria Grazia, Cominelli Fabio

机构信息

Department of Medicine, Case Western Reserve University , Cleveland, OH , USA ; Digestive Health Research Center, Case Western Reserve University , Cleveland, OH , USA.

Department of Life, Health and Environmental Sciences, University of L'Aquila , L'Aquila , Italy.

出版信息

Front Immunol. 2014 Jul 10;5:317. doi: 10.3389/fimmu.2014.00317. eCollection 2014.

Abstract

Nucleotide-binding and oligomerization domain NOD-like receptors (NLRs) are highly conserved cytosolic pattern recognition receptors that play, in combination with toll-like receptors, a critical role in innate immunity and inflammation. These proteins are characterized by a central oligomerization domain termed nucleotide-binding domain, and a protein interaction domain containing leucine-rich repeats. Some NLRs, including NOD1 and NOD2, sense the cytosolic presence of conserved bacterial molecular signatures and drive the activation of mitogen-activated protein kinase and the transcription factor NF-κB. A different set of NLRs induces caspase-1 activation through the assembly of large protein complexes known as inflammasomes. Activation of NLR proteins results in secretion of pro-inflammatory cytokines and subsequent inflammatory responses. The critical role of NLRs in innate immunity is underscored by the fact that polymorphisms within their genes are implicated in the development of several immune-mediated diseases, including inflammatory bowel disease. Over the past few years, the role of NLRs in intestinal homeostasis has been highlighted, however the mechanism by which dysfunction in these proteins leads to aberrant inflammation is still the focus of much investigation. The purpose of this review is to systematically evaluate the function of NLRs in mucosal innate immunity and understand how genetic or functional alterations in these components can lead to the disruption of intestinal homeostasis, and the subsequent development of chronic inflammation.

摘要

核苷酸结合寡聚化结构域(NOD)样受体(NLRs)是高度保守的胞质模式识别受体,与Toll样受体共同在固有免疫和炎症中发挥关键作用。这些蛋白质的特征是具有一个称为核苷酸结合结构域的中央寡聚化结构域,以及一个包含富含亮氨酸重复序列的蛋白质相互作用结构域。一些NLRs,包括NOD1和NOD2,可感知保守细菌分子信号在胞质中的存在,并驱动丝裂原活化蛋白激酶和转录因子NF-κB的激活。另一组不同的NLRs通过组装称为炎性小体的大型蛋白质复合物诱导半胱天冬酶-1的激活。NLR蛋白的激活导致促炎细胞因子的分泌及随后的炎症反应。NLRs基因内的多态性与包括炎症性肠病在内的几种免疫介导疾病的发生有关,这一事实突出了NLRs在固有免疫中的关键作用。在过去几年中,NLRs在肠道稳态中的作用已得到强调,然而这些蛋白质功能障碍导致异常炎症的机制仍是大量研究的焦点。本综述的目的是系统评估NLRs在黏膜固有免疫中的功能,并了解这些成分的基因或功能改变如何导致肠道稳态的破坏以及随后慢性炎症的发生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e535/4090755/60054de838b8/fimmu-05-00317-g001.jpg

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