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首页> 外文期刊>Frontiers in Cell and Developmental Biology >Modeling Inflammation in Zebrafish for the Development of Anti-inflammatory Drugs
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Modeling Inflammation in Zebrafish for the Development of Anti-inflammatory Drugs

机译:斑马鱼中炎症造型抗炎药

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Dysregulation of the inflammatory response in humans can lead to various inflammatory diseases, like asthma and rheumatoid arthritis. The innate branch of the immune system, including macrophage and neutrophil functions, plays a critical role in all inflammatory diseases. This part of the immune system is well conserved between humans and the zebrafish, which has emerged as a powerful animal model for inflammation, because it offers the possibility to image and study inflammatory responses in vivo at the early life stages. This review focuses on different inflammation models established in zebrafish, and how they are being used for the development of novel anti-inflammatory drugs. The most commonly used model is the tail fin amputation model, in which part of the tail fin of a zebrafish larva is clipped. This model has been used to study fundamental aspects of the inflammatory response, like the role of specific signaling pathways, the migration of leukocytes, and the interaction between different immune cells, and has also been used to screen libraries of natural compounds, approved drugs, and well-characterized pathway inhibitors. In other models the inflammation is induced by chemical treatment, such as lipopolysaccharide (LPS), leukotriene B4 (LTB4) and copper, and some chemical-induced models, such as treatment with trinitrobenzene sulfonic acid (TNBS), specifically model inflammation in the gastro-intestinal tract. Two mutant zebrafish lines, carrying a mutation in the hepatocyte growth factor activator inhibitor 1a gene (hai1a) and the cdp-diacylglycerolinositol 3-phosphatidyltransferase (cdipt) gene, show an inflammatory phenotype, and they provide interesting model systems for studying inflammation. These zebrafish inflammation models are often used to study the anti-inflammatory effects of glucocorticoids, to increase our understanding of the mechanism of action of this class of drugs and to develop novel glucocorticoid drugs. In this review, an overview is provided of the available inflammation models in zebrafish, and how they are used to unravel molecular mechanisms underlying the inflammatory response and to screen for novel anti-inflammatory drugs.
机译:人类炎症反应的失调可能导致各种炎症性疾病,如哮喘和类风湿性关节炎。免疫系统的先天分支,包括巨噬细胞和中性粒细胞功能,在所有炎症性疾病中起着关键作用。这种免疫系统之间的部分在人类和斑马鱼之间储蓄良好,这是一种强大的炎症的强大动物模型,因为它提供了在早期寿命中的体内炎症和研究炎症反应的可能性。本综述重点介绍在斑马鱼中建立的不同炎症模型,以及它们如何用于开发新型的抗炎药。最常用的模型是尾鳍截肢模型,其中斑马鱼幼虫的尾鳍的一部分被夹住。该模型已被用于研究炎症反应的基本方面,如特定信号途径,白细胞迁移的作用以及不同免疫细胞之间的相互作用,也已用于筛查天然化合物的文库,批准的药物,和特征良好的途径抑制剂。在其他模型中,通过化学处理诱导炎症,例如脂多糖(LPS),白酮B4(LTB4)和铜,以及一些化学诱导的模型,例如用三硝基苯磺酸(TNB)治疗,特别是胃肠中的模型炎症-肠道。两个突变斑马鱼线,携带肝细胞生长因子活化剂抑制剂1a基因(Hai1a)和Cdp-二酰基甘油肌醇3-磷脂酰转移酶(Cdipt)基因的突变,显示出炎症表型,并且它们为研究炎症提供有趣的模型系统。这些斑马鱼炎症模型通常用于研究糖皮质激素的抗炎作用,以提高我们对这类药物的作用机制以及开发新型糖皮质激素药物的理解。在本次审查中,提供了斑马鱼中可用炎症模型的概述,以及它们如何用于解开炎症反应潜在的分子机制和用于新型抗炎药的筛选。

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