Interleukin-18 increases TLR4 and mannose receptor expression and modulates cytokine production in human monocytes
Contribuinte(s) |
Universidade Estadual Paulista (UNESP) |
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Data(s) |
21/10/2015
21/10/2015
01/01/2015
|
Resumo |
Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) Processo FAPESP: 2007/00755-0 Processo FAPESP: 2007/04042-9 Interleukin-18 is a proinflammatory cytokine belonging to the interleukin-1 family of cytokines. This cytokine exerts many unique biological and immunological effects. To explore the role of IL-18 in inflammatory innate immune responses, we investigated its impact on expression of two toll-like receptors (TLR2 and TLR4) and mannose receptor (MR) by human peripheral blood monocytes and its effect on TNF-alpha, IL-12, IL-15, and IL-10 production. Monocytes from healthy donors were stimulated or not with IL-18 for 18 h, and then the TLR2, TLR4, and MR expression and intracellular TNF-alpha, IL-12, and IL-10 production were assessed by flow cytometry and the levels of TNF-alpha, IL-12, IL-15, and IL-10 in culture supernatants were measured by ELISA. IL-18 treatment was able to increase TLR4 and MR expression by monocytes. The production of TNF-alpha and IL-10 was also increased by cytokine treatment. However, IL-18 was unable to induce neither IL-12 nor IL-15 production by these cells. Taken together, these results show an important role of IL-18 on the early phase of inflammatory response by promoting the expression of some pattern recognition receptors (PRRs) that are important during the microbe recognition phase and by inducing some important cytokines such as TNF-alpha and IL-10. |
Formato |
9 |
Identificador |
http://www.hindawi.com/journals/mi/2015/236839/ Mediators Of Inflammation, 9 p., 2015. 0962-9351 http://hdl.handle.net/11449/128390 http://dx.doi.org/10.1155/2015/236839 WOS:000352457800001 WOS000352457800001.pdf |
Idioma(s) |
eng |
Publicador |
Hindawi Publishing Corporation |
Relação |
Mediators Of Inflammation |
Direitos |
openAccess |
Tipo |
info:eu-repo/semantics/article |