Secreted phospholipase A2-IIA-induced a phenotype of activated microglia in BV-2 cells requires epidermal growth factor receptor transactivation and proHB-EGF shedding

• Published in: Journal of neuroinflammation Vol. 9; no. 1; p. 154
• Main Authors: Martín, Rubén, Cordova, Claudia, Nieto, Maria L
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 02-07-2012; BioMed Central; BMC
• Subjects: Advertising executives; Alzheimer's disease; Analysis; Analysis of Variance; Animals; Anticoagulants (Medicine); Apoptosis; Apoptosis - drug effects; Cell Proliferation - drug effects; Cells, Cultured; Cyclooxygenase 2 - metabolism; Cytokines; Dose-Response Relationship, Drug; Enzyme Inhibitors - pharmacology; Enzymes; Epidermal growth factor; Epidermal growth factor receptor; ErbB Receptors - metabolism; Flow Cytometry; Genetic aspects; Health aspects; Heparin-binding EGF-like Growth Factor; Immune response; Intercellular Signaling Peptides and Proteins - metabolism; Kinases; Mice; Microglia; Microglia - drug effects; Microglia - metabolism; Nervous system diseases; Neurons; Phagocytosis; Phagocytosis - drug effects; Phospholipases; Phospholipases A2, Secretory - pharmacology; Phosphorylation - drug effects; Proliferation; Proteins; Rodents; Secreted phospholipase A2-IIA; Time Factors; Tumor Necrosis Factor-alpha - metabolism; Canada
• ISSN: 1742-2094; 1742-2094
• DOI: 10.1186/1742-2094-9-154

Activation of microglia, the primary component of the innate immune response in the brain, is a hallmark of neuroinflammation in neurodegenerative disorders, including Alzheimer's disease (AD) and other pathological conditions such as stroke or CNS infection. In response to a variety of insults, microglial cells produce high levels of inflammatory cytokines that are often involved in neuronal injury, and play an important role in the recognition, engulfment, and clearance of apoptotic cells and/or invading microbes. Secreted phospholipase A2-IIA (sPLA2-IIA), an enzyme that interacts with cells involved in the systemic immune/inflammatory response, has been found up-regulated in the cerebrospinal fluid and brain of AD patients. However, despite several approaches, its functions in mediating CNS inflammation remain unknown. In the present study, the role of sPLA2-IIA was examined by investigating its direct effects on microglial cells.
Primary and immortalized microglial cells were stimulated by sPLA2-IIA in order to characterize the cytokine-like actions of the phospholipase. The hallmarks of activated microglia analyzed include: mitogenic response, phagocytic capabilities and induction of inflammatory mediators. In addition, we studied several of the potential molecular mechanisms involved in those events.
The direct exposure of microglial cells to sPLA2-IIA stimulated, in a time- and dose-dependent manner, their phagocytic and proliferative capabilities. sPLA2-IIA also triggered the synthesis of the inflammatory proteins COX-2 and TNFα. In addition, EGFR phosphorylation and shedding of the membrane-anchored heparin-binding EGF-like growth factor (pro-HB-EGF) ectodomain, as well as a rapid activation/phosphorylation of the classical survival proteins ERK, P70S6K and rS6 were induced upon sPLA2-IIA treatment. We further demonstrated that the presence of an EGFR inhibitor (AG1478), a matrix metalloproteinase inhibitor (GM6001), an ADAM inhibitor (TAPI-1), and a HB-EGF neutralizing antibody abrogated the phenotype of activated microglia induced by the sPLA2-IIA.
These results support the hypothesis that sPLA2-IIA may act as a potent modulator of microglial functions through its ability to induce EGFR transactivation and HB-EGF release. Accordingly, pharmacological modulation of EGFR might be a useful tool for treating neuroinflammatory diseases characterized by sPLA2-IIA accumulation.