Department of Cell Biology, School of Life Sciences, Central South University, Changsha, 410017, China.
Xiangya Hospital, Central South University, Changsha, 410008, China.
Fish Shellfish Immunol. 2022 Jan;120:481-496. doi: 10.1016/j.fsi.2021.12.019. Epub 2021 Dec 17.
Transforming growth factor-β activated kinase-1 (TAK1) is an important upstream signaling molecules involved in the NF-κB signaling pathway. TAK1 interacts with TAB1 to form the TAK1-TAB1 complex, which elicits NF-κB activation through a series of cascade reactions in mammals. However, the function of TAK1 in blunt snout bream (Megalobrama amblycephala ( maTak1) and the effects of their interaction between TAK1 and TAB1 on the NF-κB activation still remains largely unknown. In the present study, maTak1 was cloned and characterized successfully based on transcriptome data. Its open reading frame is composed of 1626 nucleotides and the predicted maTAK1 protein contains 541 amino acids, which includes an N-terminal Serine/Threonine protein kinases (S/TKc) and a C-terminal coiled-coil region. Phylogenetic analysis showed that maTAK1 were clustered with those of other teleosts. MaTak1 displayed ubiquitous transcriptional expression in all the examined tissues of healthy blunt snout bream but with varied expression levels. And maTrak1 expression was dramatically enhanced in different tissues and MAF cells after LPS stimulation and A. hydrophila challenge. The result from subcellular localization analysis indicated that both maTAK1 and maTAB1 were cytoplasmic protein. The activity of NF-κB promoter could not be induced by overexpression of maTak1 or maTab1 alone, however, it could be enhanced by co-expression of maTak1 and maTab1. Co-immunoprecipitation and subcellular co-localization assay revealed that maTAK1 can combine with maTAB1 directly. The transcriptional expression level of pro-inflammatory cytokines (IL-1β, IL-6 and IL-8) increased distinctly after the overexpression of maTak1 and maTab1. Taken together, the data obtained in this study demonstrated that the direct interaction between maTAK1 and maTAB1 might play a pivotal role in mediating host innate immune response to pathogen invasion by the production of pro-inflammatory cytokines via NF-κB signaling pathway, which might lay a solid foundation for the establishment of novel therapeutic approach to combat bacterial infection in fish.
转化生长因子-β激活激酶 1(TAK1)是一种重要的上游信号分子,参与 NF-κB 信号通路。TAK1 与 TAB1 相互作用形成 TAK1-TAB1 复合物,在哺乳动物中通过一系列级联反应引发 NF-κB 的激活。然而,TAK1 在钝吻鲟(Megalobrama amblycephala)中的功能(maTak1)及其与 TAB1 相互作用对 NF-κB 激活的影响在很大程度上仍然未知。本研究基于转录组数据成功克隆和表征了 maTak1。其开放阅读框由 1626 个核苷酸组成,预测的 maTAK1 蛋白包含 541 个氨基酸,其中包括一个 N 端丝氨酸/苏氨酸蛋白激酶(S/TKc)和一个 C 端卷曲螺旋区。系统进化分析表明,maTAK1 与其他硬骨鱼聚类在一起。maTak1 在健康钝吻鲟的所有检测组织中均具有广泛的转录表达,但表达水平不同。并且,maTrak1 在 LPS 刺激和 A. hydrophila 攻毒后,在不同组织和 MAF 细胞中表达水平显著增强。亚细胞定位分析的结果表明,maTAK1 和 maTAB1 均为细胞质蛋白。单独过表达 maTak1 或 maTab1 不能诱导 NF-κB 启动子的活性,但共表达 maTak1 和 maTab1 可以增强 NF-κB 启动子的活性。免疫共沉淀和亚细胞共定位实验表明,maTAK1 可以与 maTAB1 直接结合。过表达 maTak1 和 maTab1 后,促炎细胞因子(IL-1β、IL-6 和 IL-8)的转录表达水平明显升高。综上所述,本研究结果表明,maTAK1 和 maTAB1 之间的直接相互作用可能通过 NF-κB 信号通路介导宿主固有免疫反应对病原体入侵产生促炎细胞因子,从而在鱼类细菌性感染的新型治疗方法的建立中奠定坚实的基础。