Functional identification and expressional responses of large yellow croaker (Larimichthys crocea) interleukin-8 and its receptor

被引:17
|
作者
Wang, Tianming [1 ]
Liang, Jing [1 ]
Xiang, Xiaowei [1 ]
Yuan, Jiajie [3 ]
Chen, Xu [1 ]
Xiang, Xingwei [2 ]
Yang, Jingwen [1 ]
机构
[1] Zhejiang Ocean Univ, Coll Marine Sci, Natl Engn Res Ctr Marine Facil Aquaculture, Zhoushan 316022, Zhejiang, Peoples R China
[2] Zhejiang Marine Dev Res Inst, Tiyu Rd 10, Zhoushan 316000, Zhejiang, Peoples R China
[3] Shaoxing Entry Exit Inspect & Quarantine Bur, Comprehens Technol Serv Ctr, Shaoxing 312000, Zhejiang, Peoples R China
关键词
Larimichthys crocea; IL-8; CXCR2; Functional interaction; Vibrio Parahemolyticus; immune response; PROTEIN-COUPLED RECEPTORS; CHEMOKINE RECEPTORS; MOLECULAR CHARACTERIZATION; NEUTROPHIL RECRUITMENT; CELL PROLIFERATION; CXC CHEMOKINE; KINASES; CLONING; CANCER; GROWTH;
D O I
10.1016/j.fsi.2019.01.035
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
Interleukin-8 (IL-8 or chemokine (C-X-C motif) ligand 8, CXCL8) is a chemokine produced by multiple cell types. It promotes chemotaxis and phagocytosis via interaction with chemokine receptors CXCR1 and CXCR2. Using published data, IL-8 gene (LcIL-8) of the large yellow croaker (Larimichthys crocea) was cloned into the pcDNA3.1 plasmid, and an interleukin-8 receptor (LcCXCR2) was cloned into the pEGFP-N1 plasmid. Secratory expression of LcIL-8 in HEK293T cells was carried out, and product in culture medium was collected for LcCXCR2 stimulation in HEK293 cells. Following receptor internalization observation and intracellular signaling detection, the functional interaction of LcIL-8 and LcCXCR2 was further determined and the ERK phosphorylation signal activation mediated by LcCXCR2 was demonstrated. Quantitative real-time PCR analysis was used to analyze transcription level regulation of LcIL-8 and LcCXCR2 in various tissues of large yellow croaker. Expression of LcIL-8 and LcCXCR2 was elevated in the spleen, head kidney, and liver after Vibrio parahemolyticus challenge. Results illustrated the functional interaction between LcIL-8 and LcCXCR2 in mediating intracellular ERK1/2 phosphorylation signaling and suggested that the LcIL-8 and LcCXCR2 system is part of the immune response induced by V. Parahemolyticus in L. crocea.
引用
收藏
页码:470 / 477
页数:8
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