Ding Yang, Ao Jingqun, Chen Xinhua
College of Animal Sciences, Fujian Agriculture and Forestry University, Fuzhou 350002, PR China; Key Laboratory of Marine Biogenetic Resources, Third Institute of Oceanography, State Oceanic Administration, Xiamen 361005, PR China; Fujian Collaborative Innovation Center for Exploitation and Utilization of Marine Biological Resources, Xiamen 361005, PR China.
College of Animal Sciences, Fujian Agriculture and Forestry University, Fuzhou 350002, PR China; Key Laboratory of Marine Biogenetic Resources, Third Institute of Oceanography, State Oceanic Administration, Xiamen 361005, PR China; Fujian Collaborative Innovation Center for Exploitation and Utilization of Marine Biological Resources, Xiamen 361005, PR China; Laboratory for Marine Biology and Biotechnology, Qingdao National Laboratory for Marine Science and Technology, Qingdao 266071, PR China.
Dev Comp Immunol. 2017 Nov;76:34-44. doi: 10.1016/j.dci.2017.05.014. Epub 2017 May 16.
Interleukin 17 (IL-17) family members are key players in regulating the immune response in mammals. Here, we identified the IL-17C and IL-17D homologs from large yellow croaker (Larimichthys crocea), named LcIL-17C and LcIL-17D, respectively. The deduced LcIL-17C and LcIL-17D proteins possessed the typical IL-17 domain and shared a conserved arrangement of eight cysteine residues. Both LcIL-17C and LcIL-17Dc genes were constitutively expressed in all tissues examined, although at different levels. After challenge with Aeromonas hydrophila, the expression of LcIL-17C and LcIL-17D was significantly increased in gills, head kidney, and spleen. In the peripheral blood leukocytes (PBLs), the recombinant LcIL-17C (rLcIL-17C) could strongly promote the expression of chemokines (CXCL8, CXCL12, and CXCL13), proinflammatory factors (TNF-α, IL-1β, IL-6, and IFNg), and antibacterial peptide hepcidin, whereas rLcIL-17D induced a weaker expression of these chemokines. Consistently, the culture supernatants from the PBLs treated by rLcIL-17C showed a stronger ability to induce the migration of PBLs than those treated by rLcIL-17D. Furthermore, both rLcIL-17C and rLcIL-17D could activate the NF-κB signalling in the epithelioma papulosum cyprini (EPC) cells. Taken together, these results indicated that LcIL-17C and LcIL-17D, although differing in their ability to mediate chemotaxis for PBLs, may promote the inflammatory response and host defence via activating NF-κB signalling. To our knowledge, this is the first report on functional identification of a IL-17C in teleost.
白细胞介素17(IL-17)家族成员是调节哺乳动物免疫反应的关键因子。在此,我们从大黄鱼(Larimichthys crocea)中鉴定出IL-17C和IL-17D的同源物,分别命名为LcIL-17C和LcIL-17D。推导的LcIL-17C和LcIL-17D蛋白具有典型的IL-17结构域,并共享八个半胱氨酸残基的保守排列。LcIL-17C和LcIL-17Dc基因在所有检测的组织中均组成性表达,尽管表达水平不同。在用嗜水气单胞菌攻击后,LcIL-17C和LcIL-17D在鳃、头肾和脾脏中的表达显著增加。在外周血白细胞(PBL)中,重组LcIL-17C(rLcIL-17C)可强烈促进趋化因子(CXCL8、CXCL12和CXCL13)、促炎因子(TNF-α、IL-1β、IL-6和IFNg)以及抗菌肽铁调素的表达,而rLcIL-17D诱导这些趋化因子的表达较弱。一致地,rLcIL-17C处理的PBL培养上清液比rLcIL-17D处理的上清液表现出更强的诱导PBL迁移的能力。此外,rLcIL-17C和rLcIL-17D均可激活鲤上皮瘤(EPC)细胞中的NF-κB信号通路。综上所述,这些结果表明,LcIL-17C和LcIL-17D虽然在介导PBL趋化性的能力上有所不同,但可能通过激活NF-κB信号通路促进炎症反应和宿主防御。据我们所知,这是关于硬骨鱼中IL-17C功能鉴定的首次报道。