CXCL9-11 chemokines and CXCR3 receptor in teleost fish species

Natalia Valdés , Marcos Cortés , Felipe Barraza , Felipe E. Reyes-López , Mónica Imarai
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引用次数: 1

Abstract

The coordinated migration of immune cells from lymphoid organs to in or out of the bloodstream, and towards the site of infection or tissue damage is fundamental for an efficient innate and adaptive immune response. Interestingly, an essential part of this movement is mediated by chemoattractant cytokines called chemokines. Although the nature and function of chemokines and their receptors are well documented in mammals, much research is needed to accomplish a similar level of understanding of the role of chemokines in fish immunity. The first chemokine gene identified in teleosts (rainbow trout, Oncorhynchus mykiss) was CK1 in 1998. Since then, the identification of fish chemokine orthologue genes and characterization of their role has been more complex than expected, primarily because of the whole genome duplication processes occurring in fish, and because chemokines evolve faster than other immune genes. Some of the most studied chemokines are CXCL9, CXCL10, CXCL11, and the CXCR3 receptor, all involved in T cell migration and in the induction of the T helper 1 (Th1) immune response. Data from the zebrafish and rainbow trout CXCL9-11/CXCR3 axis suggest that these chemokines and the receptor arose early in evolution and must be present in most teleost fish. However, the pieces of knowledge also indicate that different numbers of gene copies can be present in different species, with distinct regulatory expression mechanisms and probably, also with different roles, as the differential expression in fish tissues suggest. Here, we revised the current knowledge of the CXCL9-11/CXCR3 axis in teleost fishes, identifying the gaps in knowledge, and raising some hypotheses for the role of CXCL9, CXCL10 CXCL11, and CXCR3 receptor axis in fish, which can encourage further studies in the field.

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硬骨鱼中CXCL9-11趋化因子和CXCR3受体
免疫细胞从淋巴器官向血流内或血流外、向感染部位或组织损伤方向的协调迁移是有效的先天和适应性免疫反应的基础。有趣的是,这种运动的一个重要部分是由称为趋化因子的趋化因子介导的。虽然趋化因子及其受体的性质和功能在哺乳动物中有很好的记载,但要对趋化因子在鱼类免疫中的作用有类似的认识,还需要进行大量的研究。1998年首次在硬骨鱼(虹鳟、Oncorhynchus mykiss)中发现趋化因子基因CK1。从那时起,鱼类趋化因子同源基因的鉴定及其作用的表征比预期的要复杂得多,主要是因为鱼类中发生的全基因组复制过程,以及趋化因子比其他免疫基因进化得更快。一些研究最多的趋化因子是CXCL9, CXCL10, CXCL11和CXCR3受体,它们都参与T细胞迁移和诱导T辅助1 (Th1)免疫反应。来自斑马鱼和虹鳟鱼CXCL9-11/CXCR3轴的数据表明,这些趋化因子和受体在进化早期出现,并且必须存在于大多数硬骨鱼中。然而,这些知识也表明,不同物种中可能存在不同数量的基因拷贝,具有不同的调控表达机制,并且可能具有不同的作用,正如鱼类组织中的差异表达所表明的那样。本文对硬骨鱼中CXCL9-11/CXCR3受体轴的现有知识进行了修订,确定了知识的空白,并对CXCL9、CXCL10、CXCL11和CXCR3受体轴在鱼类中的作用提出了一些假设,以期促进该领域的进一步研究。
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CiteScore
2.60
自引率
0.00%
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0
审稿时长
12 weeks
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