Comparative study of interleukin-17C (IL-17C) and IL-17D in large yellow croaker Larimichthys crocea reveals their similar but differential functional activity

被引:39
作者
Ding, Yang [1 ,2 ,3 ]
Ao, Jingqun [1 ,2 ,3 ]
Chen, Xinhua [1 ,2 ,3 ,4 ]
机构
[1] Fujian Agr & Forestry Univ, Coll Anim Sci, Shangxiadian Rd 15, Fuzhou 350002, Peoples R China
[2] State Ocean Adm, Inst Oceanog 3, Key Lab Marine Biogenet Resources, Xiamen 361005, Peoples R China
[3] Fujian Collaborat Innovat Ctr Exploitat & Utiliza, Xiamen 361005, Peoples R China
[4] Qingdao Natl Lab Marine Sci & Technol, Lab Marine Biol & Biotechnol, Qingdao 266071, Peoples R China
基金
中国国家自然科学基金;
关键词
Large yellow croaker (Larimichthys crocea); Interleukin-17C and D; Molecular characterization; Functional analysis; MOLECULAR CHARACTERIZATION; FAMILY CYTOKINES; EPITHELIAL-CELLS; RECEPTOR GENES; IDENTIFICATION; CLONING; MEMBERS; FISH; INFECTION; LIGAND;
D O I
10.1016/j.dci.2017.05.014
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
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 LdL-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-alpha, IL-beta, 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-kappa B 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-kappa B signalling. To our knowledge, this is the first report on functional identification of a IL-17C in teleost. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:34 / 44
页数:11
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