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Updated: Aug 23, 2026

Generation of Immature, Mature and Tolerogenic Dendritic Cells with Differing Metabolic Phenotypes
Published on: June 22, 2016
Secretory phospholipase A2 induces dendritic cell maturation
Laure Perrin-Cocon1, Sophie Agaugué, Frédéric Coutant
1Institut Fédératif de Recherche 128, Institut National de la Santé et de la Recherche Médicale Unit 503, F-69365 Lyon Cedex 07, France.
Abstract:
High level of phospholipase A(2) (PLA(2)) activity is found in serum and biological fluids during the acute-phase response (APR). Extracellular PLA(2) in fluids of patients with inflammatory diseases such as sepsis, acute pancreatitis or rheumatoid arthritis is also associated with propagation of inflammation. PLA(2) activity is involved in the release of both pro- and anti-inflammatory lipid mediators from phospholipids of cellular membranes or circulating lipoproteins. PLA(2) may thus generate signals that influence immune responses. Here, group III secretory PLA(2) were tested for their ability to promote generation of functionally mature human dendritic cells (DC). PLA(2) treatment of differentiating monocytes in the presence of granulocyte/macrophage colony-stimulating factor and IL-4 yielded cells with phenotypical and functional characteristics of mature DC. This maturation was dependent on the dose of PLA(2), and PLA(2)-generated DC stimulated IFN-gamma secretion by allogeneic T cells. The effects of PLA(2) on DC maturation was mainly dependent on enzyme activity and correlated with the activation of NF-kappaB, AP-1 and NFAT. The data suggest that transient increase in PLA(2) activity generates signals that promote transition of innate to adaptive immunity during the APR.
Insights
Phospholipase A(2) (PLA(2)) promotes the development of mature dendritic cells (DC) during the acute-phase response. This enzyme activity is crucial for bridging innate and adaptive immunity.
Area of Science:
- Immunology
- Biochemistry
Background:
- Phospholipase A(2) (PLA(2)) activity is elevated during the acute-phase response (APR) and linked to inflammatory diseases.
- Extracellular PLA(2) contributes to inflammation propagation by releasing lipid mediators.
Purpose of the Study:
- To investigate the role of group III secretory PLA(2) in the generation of mature human dendritic cells (DC).
Main Methods:
- Monocytes were treated with PLA(2) in the presence of GM-CSF and IL-4.
- Phenotypical and functional characteristics of mature DC were assessed.
- NF-kappaB, AP-1, and NFAT activation were analyzed.
Main Results:
- PLA(2) treatment induced the generation of functionally mature human DC.
- Maturation was dose-dependent and correlated with enzyme activity.
- PLA(2)-generated DC stimulated IFN-gamma secretion by T cells, indicating activation of adaptive immunity.
Conclusions:
- PLA(2) plays a significant role in DC maturation.
- This process involves the activation of transcription factors like NF-kappaB, AP-1, and NFAT.
- PLA(2) activity may facilitate the transition from innate to adaptive immunity during the APR.
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