Xie Yufei, Meijer Annemarie H, Schaaf Marcel J M
Institute of Biology Leiden, Leiden University, Leiden, Netherlands.
Front Cell Dev Biol. 2021 Jan 15;8:620984. doi: 10.3389/fcell.2020.620984. eCollection 2020.
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 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 () and the cdp-diacylglycerolinositol 3-phosphatidyltransferase () 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.
人类炎症反应失调可导致多种炎症性疾病,如哮喘和类风湿性关节炎。免疫系统的固有分支,包括巨噬细胞和中性粒细胞的功能,在所有炎症性疾病中都起着关键作用。人类和斑马鱼的这部分免疫系统高度保守,斑马鱼已成为一种强大的炎症动物模型,因为它能够在生命早期阶段对炎症反应进行成像和研究。本综述重点关注在斑马鱼中建立的不同炎症模型,以及它们如何被用于开发新型抗炎药物。最常用的模型是尾鳍截肢模型,即剪掉斑马鱼幼虫的部分尾鳍。该模型已被用于研究炎症反应的基本方面,如特定信号通路的作用、白细胞的迁移以及不同免疫细胞之间的相互作用,还被用于筛选天然化合物库、已批准药物和特征明确的通路抑制剂。在其他模型中,炎症是通过化学处理诱导的,如脂多糖(LPS)、白三烯B4(LTB4)和铜,一些化学诱导模型,如用三硝基苯磺酸(TNBS)处理,专门模拟胃肠道炎症。两个突变斑马鱼品系,分别在肝细胞生长因子激活剂抑制剂1a基因()和cdp - 二酰甘油 - 肌醇3 - 磷脂酰转移酶()基因中发生突变,表现出炎症表型,它们为研究炎症提供了有趣的模型系统。这些斑马鱼炎症模型常被用于研究糖皮质激素的抗炎作用,以加深我们对这类药物作用机制的理解,并开发新型糖皮质激素药物。在本综述中,概述了斑马鱼中可用的炎症模型,以及它们如何被用于揭示炎症反应的分子机制和筛选新型抗炎药物。