Essential role for epidermal growth factor receptor in glutamate receptor signaling to NF-kappaB

• Published in: Molecular and cellular biology 2008-08, Vol.28 (16), p.5061
• Main Authors: Sitcheran, Raquel, Comb, William C, Cogswell, Patricia C, Baldwin, Albert S
• Format: Article
• Language: English
• Subjects: Animals; Calcium Signaling - drug effects; Cell Line; Cell Nucleus - drug effects; Cell Nucleus - metabolism; Cell Proliferation - drug effects; Glutamic Acid - pharmacology; Glycine - analogs & derivatives; Glycine - pharmacology; Humans; I-kappa B Kinase - metabolism; I-kappa B Proteins - metabolism; Intracellular Space - drug effects; Intracellular Space - metabolism; Mice; Neuroglia - cytology; Neuroglia - drug effects; Neuroglia - metabolism; Phenylacetates - pharmacology; Phosphorylation - drug effects; Protein Processing, Post-Translational - drug effects; Receptor, Epidermal Growth Factor - metabolism; Receptor, Metabotropic Glutamate 5; Receptors, Glutamate - metabolism; Receptors, Metabotropic Glutamate - metabolism; Signal Transduction - drug effects; Transcription Factor RelA - metabolism; Transcriptional Activation - drug effects
• ISSN: 1098-5549
• DOI: 10.1128/MCB.00578-08

Glutamate is a critical neurotransmitter of the central nervous system (CNS) and also an important regulator of cell survival and proliferation. The binding of glutamate to metabotropic glutamate receptors induces signal transduction cascades that lead to gene-specific transcription. The transcription factor NF-kappaB, which regulates cell proliferation and survival, is activated by glutamate; however, the glutamate receptor-induced signaling pathways that lead to this activation are not clearly defined. Here we investigate the glutamate-induced activation of NF-kappaB in glial cells of the CNS, including primary astrocytes. We show that glutamate induces phosphorylation, nuclear accumulation, DNA binding, and transcriptional activation function of glial p65. The glutamate-induced activation of NF-kappaB requires calcium-dependent IkappaB kinase alpha (IKKalpha) and IKKbeta activation and induces p65-IkappaBalpha dissociation in the absence of IkappaBalpha phosphorylation or degradation. Moreover, glutamate-induced IKK preferentially targets the phosphorylation of p65 but not IkappaBalpha. Finally, we show that the ability of glutamate to activate NF-kappaB requires cross-coupled signaling with the epidermal growth factor receptor. Our results provide insight into a glutamate-induced regulatory pathway distinct from that described for cytokine-induced NF-kappaB activation and have important implications with regard to both normal glial cell physiology and pathogenesis.