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Molecular cloning, characterization and mRNA expression of duck interleukin-17F

Authors
Kim, Woo H.Fernandez, Cherry P.Diaz, Joyce Anne R.Jeong, JipseolKim, SukLillehoj, Hyun S.Chang, Hong H.Min, Wongi
Issue Date
15-Apr-2015
Publisher
ELSEVIER
Keywords
Duck; Cytokine; Salmonella infection; Interleukin-17F
Citation
VETERINARY IMMUNOLOGY AND IMMUNOPATHOLOGY, v.164, no.3-4, pp.194 - 200
Indexed
SCIE
SCOPUS
Journal Title
VETERINARY IMMUNOLOGY AND IMMUNOPATHOLOGY
Volume
164
Number
3-4
Start Page
194
End Page
200
URI
https://scholarworks.bwise.kr/gnu/handle/sw.gnu/17297
DOI
10.1016/j.vetimm.2015.02.007
ISSN
0165-2427
Abstract
Interleukin-17F (IL-17F) is a proinflammatory cytokine that plays an important role in gut homeostasis. A full-length duck IL-17F (dulL-17F) cDNA with a 510-bp coding region was identified in ConA-activated splenic lymphocytes. dulL-17F is predicted to encode 166 amino acids, including a 26-amino acid signal peptide, a single N-linked glycosylation site, and six cysteine residues that are conserved in mammalian IL-17. dulL-17F shares 77.5% amino acid sequence identity with chicken IL-17F (chIL-17F), 37-46% with corresponding mammalian homologues, and 53.5% with the previously described duck IL-17A (duIL-17A). The duIL-17F transcripts were expressed in a wide range of untreated tissues; levels were highest in the liver and moderate in the thymus, bursa, kidney, and intestinal tissues. Expression levels of duIL-17F transcript were slightly up-regulated in ConA- and LPS-activated splenic lymphocytes but not in poly I:C stimulated cells. duIL-17F forms heterodimers with dulL-17A. Recombinant dulL-17F, like dulL-17A, induced IL-1 beta, IL-6, and IL-8 expression in duck embryonic fibroblasts (DEFs). dulL-17A, but not duIL-17F expression, was significantly up-regulated in the liver and spleen of Salmonella Typhimurium-infected ducks. Further analysis of the contributions of IL-17F to different Salmonella spp. or other disease models will be required to expand our understanding of its biological functions. (C) 2015 Elsevier B.V. All rights reserved.
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