Functional identification and expressional responses of large yellow croaker (Larimichthys crocea) interleukin-8 and its receptor.
CXCR2
Functional interaction
IL-8
Larimichthys crocea
Vibrio Parahemolyticus
immune response
Journal
Fish & shellfish immunology
ISSN: 1095-9947
Titre abrégé: Fish Shellfish Immunol
Pays: England
ID NLM: 9505220
Informations de publication
Date de publication:
Apr 2019
Apr 2019
Historique:
received:
11
11
2018
revised:
19
01
2019
accepted:
25
01
2019
pubmed:
2
2
2019
medline:
3
7
2019
entrez:
2
2
2019
Statut:
ppublish
Résumé
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.
Identifiants
pubmed: 30708055
pii: S1050-4648(19)30051-8
doi: 10.1016/j.fsi.2019.01.035
pii:
doi:
Substances chimiques
Fish Proteins
0
Interleukin-8
0
Receptors, Interleukin-8A
0
Receptors, Interleukin-8B
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
470-477Informations de copyright
Copyright © 2019 Elsevier Ltd. All rights reserved.