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The fish oil ingredient, docosahexaenoic acid, activates cytosolic phospholipase A2 via GPR120 receptor to produce prostaglandin E2 and plays an anti-inflammatory role in macrophages.

Authors :
Liu, Yueqin
Chen, Li‐Yuan
Sokolowska, Milena
Eberlein, Michael
Alsaaty, Sara
Martinez‐Anton, Asuncion
Logun, Carolea
Qi, Hai‐Yan
Shelhamer, James H.
Source :
Immunology; Sep2014, Vol. 143 Issue 1, p81-95, 15p
Publication Year :
2014

Abstract

Docosahexaenoic acid (DHA) is one of the major ingredients of fish oil and has been reported to have anti-inflammatory properties mediated through the GPR120 receptor. Whether cytosolic phospholipase A<subscript>2</subscript> ( cPLA<subscript>2</subscript>) and lipid mediators produced from cPLA<subscript>2</subscript> activation are involved in the anti-inflammatory role of DHA in macrophages has not been reported. We report here that DHA and the GPR120 agonist, GW9508, activate cPLA<subscript>2</subscript> and cyclooxygenase 2 (COX-2), and cause prostaglandin E<subscript>2</subscript> (PGE<subscript>2</subscript>) release in a murine macrophage cell line RAW264.7 and in human primary monocyte-derived macrophages. DHA and GW9508 activate cPLA<subscript>2</subscript> via GPR120 receptor, G protein G αq and scaffold protein β-arrestin 2. Extracellular signal-regulated kinase 1/2 activation is involved in DHA- and GW9508-induced cPLA<subscript>2</subscript> activation, but not p38 mitogen-activated protein kinase. The anti-inflammatory role of DHA and GW9508 is in part via activation of cPLA<subscript>2</subscript>, COX-2 and production of PGE<subscript>2</subscript> as a cPLA<subscript>2</subscript> inhibitor or a COX-2 inhibitor partially reverses the DHA- and GW9508-induced inhibition of lipopolysaccharide-induced interleukin-6 secretion. The cPLA<subscript>2</subscript> product arachidonic acid and PGE<subscript>2</subscript> also play an anti-inflammatory role. This effect of PGE<subscript>2</subscript> is partially through inhibition of the nuclear factor-κB signalling pathway and through the EP4 receptor of PGE<subscript>2</subscript> because an EP4 inhibitor or knock-down of EP4 partially reverses DHA inhibition of lipopolysaccharide-induced interleukin-6 secretion. Hence, DHA has an anti-inflammatory effect partially through induction of PGE<subscript>2</subscript>. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00192805
Volume :
143
Issue :
1
Database :
Complementary Index
Journal :
Immunology
Publication Type :
Academic Journal
Accession number :
97240944
Full Text :
https://doi.org/10.1111/imm.12296