Lipin-1 Integrates Lipid Synthesis with Proinflammatory Responses during TLR Activation in Macrophages
Author(s) -
Clara Meana,
Lucía Peña,
Gema Lordén,
Esperanza Esquinas,
Carlos Guijas,
Martín Valdearcos,
Jesús Balsinde,
Marı́a A. Balboa
Publication year - 2014
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.1400238
Subject(s) - proinflammatory cytokine , phosphatidic acid , diacylglycerol kinase , mediator , microbiology and biotechnology , macrophage , tlr4 , phosphatase , chemistry , biology , biochemistry , signal transduction , inflammation , phosphorylation , immunology , in vitro , phospholipid , protein kinase c , membrane
Lipin-1 is a Mg(2+)-dependent phosphatidic acid phosphatase involved in the de novo synthesis of phospholipids and triglycerides. Using macrophages from lipin-1-deficient animals and human macrophages deficient in the enzyme, we show in this work that this phosphatase acts as a proinflammatory mediator during TLR signaling and during the development of in vivo inflammatory processes. After TLR4 stimulation lipin-1-deficient macrophages showed a decreased production of diacylglycerol and activation of MAPKs and AP-1. Consequently, the generation of proinflammatory cytokines like IL-6, IL-12, IL-23, or enzymes like inducible NO synthase and cyclooxygenase 2, was reduced. In addition, animals lacking lipin-1 had a faster recovery from endotoxin administration concomitant with a reduced production of harmful molecules in spleen and liver. These findings demonstrate an unanticipated role for lipin-1 as a mediator of macrophage proinflammatory activation and support a critical link between lipid biosynthesis and systemic inflammatory responses.
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