Zebrafish FKBP5 facilitates apoptosis and SVCV propagation by suppressing NF-κB signaling pathway

IF 4.1 2区 农林科学 Q1 FISHERIES
Zijia Yin , Hongying Zhang , Kaiwen Zhao , Yulong Liu , Ru Guo , Pengxia Xu , Guannan Zhao , Menglei Hu , Chengyu Hu , Xiaowen Xu
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引用次数: 0

Abstract

FK506-binding protein 5 (FKBP5), encoded by FKBP5 gene, has been reported as a scaffolding protein in various mammalian pathways related to immunity, inflammation, apoptosis and autophagy. However, the role of FKBP5 in lower vertebrates remains unknown. In this study, we identified zebrafish FKBP5 (DrFKBP5), an ortholog of mammalian FKBP5, which shows high homology with its counterpart in Anabarilius grahami based on amino acid alignment and phylogenetic analysis. DrFKBP5 was found to express ubiquitously across all tested tissues. Its expression were significantly upregulated in eye, intestine, gill, skin, heart, liver and kidney following SVCV treatment. A similar expression pattern was also observed in EPC and ZFIN cells. DrFKBP5 decreased the promoter activitiy of NF-κB and IL-6 rather than IFN I. It also inhibited the expression of inflammatory factor genes such as IL-6, IL-1β and TNF-α. In molecular mechanism, we found that DrFKBP5 interacted with IKKβ (an activator of NF-κB pathway), but not with IKKα or IKKγ, suggesting that DrFKBP5 regulates NF-κB pathway by targeting IKKβ. Then, DrFKBP5 significantly reduced the phosphorylation of IKKβ. Furthermore, it inhibited SVCV-induced nuclear translocation, phosphorylation of p65 and promoted SVCV replication in ZFIN cells. Finally, DrFKBP5 activated the expression of apoptosis-related genes, including BAX, Bcl2, caspase-3 and induced apoptosis under SVCV treatment.
斑马鱼 FKBP5 通过抑制 NF-κB 信号通路促进细胞凋亡和 SVCV 传播。
据报道,由 FKBP5 基因编码的 FK506 结合蛋白 5(FKBP5)是哺乳动物免疫、炎症、细胞凋亡和自噬相关通路中的一个支架蛋白。然而,FKBP5在低等脊椎动物中的作用仍然未知。在这项研究中,我们鉴定了斑马鱼 FKBP5(DrFKBP5),它是哺乳动物 FKBP5 的直向同源物,根据氨基酸比对和系统发育分析,它与 Anabarilius grahami 中的同源物显示出高度的同源性。研究发现,DrFKBP5在所有受测组织中均有普遍表达。经 SVCV 处理后,DrFKBP5 在眼、肠、鳃、皮肤、心脏、肝脏和肾脏中的表达明显上调。在 EPC 和 ZFIN 细胞中也观察到类似的表达模式。DrFKBP5降低了NF-κB和IL-6的启动子活性,而不是IFN I,它还抑制了炎症因子基因如IL-6、IL-1β和TNF-α的表达。在分子机制方面,我们发现DrFKBP5与IKKβ(NF-κB通路的激活因子)相互作用,而与IKKα或IKKγ没有相互作用,这表明DrFKBP5通过靶向IKKβ来调控NF-κB通路。随后,DrFKBP5 显著降低了 IKKβ 的磷酸化。此外,它还抑制了 SVCV 诱导的核转位和 p65 的磷酸化,并促进了 ZFIN 细胞中 SVCV 的复制。最后,DrFKBP5 能激活细胞凋亡相关基因的表达,包括 BAX、Bcl2 和 caspase-3,并在 SVCV 处理下诱导细胞凋亡。
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来源期刊
Fish & shellfish immunology
Fish & shellfish immunology 农林科学-海洋与淡水生物学
CiteScore
7.50
自引率
19.10%
发文量
750
审稿时长
68 days
期刊介绍: Fish and Shellfish Immunology rapidly publishes high-quality, peer-refereed contributions in the expanding fields of fish and shellfish immunology. It presents studies on the basic mechanisms of both the specific and non-specific defense systems, the cells, tissues, and humoral factors involved, their dependence on environmental and intrinsic factors, response to pathogens, response to vaccination, and applied studies on the development of specific vaccines for use in the aquaculture industry.
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