期刊
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS
卷 1863, 期 10, 页码 1297-1304出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/j.bbalip.2018.07.003
关键词
Prostaglandin EP4 receptor; Inflammatory activation; Human monocytic cells; Tumor necrosis factor
资金
- Ministry of Higher Education of Saudi Arabia
Prostaglandin E-2 (PGE(2)) is responsible for inflammatory symptoms. However, PGE(2) also suppresses pro-inflammatory cytokine production. There are at least 4 subtypes of PGE(2) receptors, EP1-EP4, but it is unclear which of these specifically control cytokine production. The aim of this study was to determine which of the different receptors, EP1R-EP4R modulate production of tumor necrosis factor-alpha (TNF-alpha) in human monocytic cells. Human blood, or the human monocytic cell line THP-1 were stimulated with LPS. The actions of PGE(2), alongside selective agonists of EP1-EP4 receptors, were assessed on LPS-induced TNF-alpha, IL-beta and IL-10 release. The expression profiles of EP2R and EP4R in monocytes and THP-1 cells were characterised by RT-qPCR. In addition, the production of cytokines was evaluated following knockdown of the receptors using siRNA and over-expression of the receptors by transfection with constructs. PGE(2) and also EP2 and EP4 agonists (but not EP1 or EP3 agonists) suppressed TNF-alpha production in blood and THP-1 cells. LPS also up regulated expression of EP2R and EP4R but not EP1 or EP3. siRNA for either EP2R or EP4R reversed the suppressive actions of PGE(2) on cytokine production and overexpression of EP2R and EP4R enhanced the suppressive actions of PGE(2). This indicates that PGE(2) suppression of TNF-alpha by human monocytic cells occurs via EP2R and EP4R expression. However EP4Rs also control their own expression and that of EP2 whereas the EP2R does not affect EP4R expression. This implies that EP4 receptors have an important master role in controlling inflammatory responses.
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