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模式识别受体与固有免疫的调控:核酸的作用

Pattern Recognition Receptors and Control of Innate Immunity: Role of Nucleic Acids.

作者信息

Fischer Silvia

机构信息

Institute of Biochemistry, Medical School, Justus-Liebig-University, Giessen 35392, Germany.

出版信息

Curr Pharm Biotechnol. 2018;19(15):1203-1209. doi: 10.2174/138920112804583087.

Abstract

The innate immune system protects against infectious microbes by the recognition of pathogen- associated molecular patterns, which serve to detect pathogens on the host cell surface or in endosomes by pattern recognition receptors such as Toll-like receptors, nucleotide-binding oligomerization domain-containing protein-1-like receptors, mannose-receptor, or retinoic acid-inducible gene-1- like receptors that initiate proper host defense mechanisms. In addition to pathogen-associated molecular patterns, a series of endogenous danger-associated molecular patterns, such as nucleic acids, are recognized by pattern recognition receptors, which serve as body´s own alarm signals under sterile conditions, such as ischemic injuries, trauma, tumors, tissue transplants, or autoimmune diseases. Thus, exogenous as well as endogenous nucleic acids can function as "alarmins" to alert the body about danger or disease by triggering inflammation, dendritic cell maturation, and stimulate the immune response resulting in the release of cytokines, which in turn can augment the local inflammatory environment. Moreover, danger-associated molecular patterns such as nucleic acids can act as cofactor in the activation of pattern recognition receptors in situations of cellular stress or upon infection leading to a massive amplification of the inflammatory response. As a consequence, acute and also chronic inflammatory diseases such as rheumatoid arthritis, cancer, or atherosclerosis may depend on such perpetuated proinflammatory responses involving activities of nucleic acids. As antagonists, RNase1 or DNase administration or nucleic acid complexing agents may result in a significant blockade of the outcome of particular pathological situations and in considerable tissue protection.

摘要

先天性免疫系统通过识别病原体相关分子模式来抵御传染性微生物,这些模式可通过Toll样受体、含核苷酸结合寡聚化结构域蛋白1样受体、甘露糖受体或维甲酸诱导基因1样受体等模式识别受体在宿主细胞表面或内体中检测病原体,从而启动适当的宿主防御机制。除了病原体相关分子模式外,一系列内源性危险相关分子模式,如核酸,也被模式识别受体识别,在缺血性损伤、创伤、肿瘤、组织移植或自身免疫性疾病等无菌条件下,这些模式作为机体自身的警报信号。因此,外源性和内源性核酸都可以作为“警报素”,通过引发炎症、树突状细胞成熟并刺激免疫反应,导致细胞因子释放,进而增强局部炎症环境,来提醒机体注意危险或疾病。此外,在细胞应激或感染情况下,核酸等危险相关分子模式可作为模式识别受体激活的辅助因子,导致炎症反应的大量放大。因此,类风湿性关节炎、癌症或动脉粥样硬化等急性和慢性炎症性疾病可能依赖于涉及核酸活性的这种持续的促炎反应。作为拮抗剂,给予核糖核酸酶1或脱氧核糖核酸酶或核酸络合剂可能会显著阻断特定病理情况的结果,并提供相当程度的组织保护。

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