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Cited 2 time in webofscience Cited 4 time in scopus
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Downregulation of common cytokine receptor gamma chain inhibits inflammatory responses in macrophages stimulated with Riemerella anatipestifer

Authors
Afrin, FahmidaFernandez, Cherry P.Flores, Rochelle A.Kim, Woo H.Jeong, JipseolChang, Hong H.Kim, SukLillehoj, Hyun S.Min, Wongi
Issue Date
Apr-2018
Publisher
ELSEVIER SCI LTD
Keywords
Ducks; Riemerella anatipestifer infection; Common cytokine receptor gamma chain; Inflammatory cytokines; Small interfering RNAs
Citation
DEVELOPMENTAL AND COMPARATIVE IMMUNOLOGY, v.81, pp.225 - 234
Indexed
SCIE
SCOPUS
Journal Title
DEVELOPMENTAL AND COMPARATIVE IMMUNOLOGY
Volume
81
Start Page
225
End Page
234
URI
https://scholarworks.bwise.kr/gnu/handle/sw.gnu/11745
DOI
10.1016/j.dci.2017.12.009
ISSN
0145-305X
Abstract
Th17-cell-mediated inflammation is affected by the soluble form of common cytokine receptor gamma chain (gamma(c)). We previously suggested that inflammatory cytokines including interleukin (IL)-17A are associated with Riemerella anatipestifer infection, which a harmful bacterial pathogen in ducks. Here, the expression profiles of membrane-associated gamma(c) (du gamma(c)-a) and soluble gamma(c) (du gamma(c)-b) in R. anatipestifer-stimulated splenic lymphocytes and macrophages, and in the spleens and livers of R. anatipestifer-infected ducks, were investigated. In vitro and in vivo results indicated that the expression levels of both forms of gamma(c) were increased, showing that marked increases were detected in the expression of the du gamma(c)-b form rather than the du gamma(c)-a form. Treatment with gamma(c)-specific siRNA downregulated mRNA expression of Th17-related cytokines, including IL -17A and IL-17F, in duck splenic macrophages stimulated with R. anatipestifer, whereas the expressions of interferon (IFN)-gamma and IL-2 were enhanced. The results showed that the upregulation of gamma(c), especially the du gamma(c)-b form, was associated with expression of Th17-related cytokines during R. anatipestifer infection. (C) 2017 Elsevier Ltd. All rights reserved.
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