Journal
JOURNAL OF NEUROCHEMISTRY
Volume 96, Issue 2, Pages 335-348Publisher
WILEY
DOI: 10.1111/j.1471-4159.2005.03543.x
Keywords
cell death; extrasynaptic; glutamate receptors; N-methyl-D-aspartate receptor subunit 2B; survival
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Funding
- NCRR NIH HHS [P20-RR15576] Funding Source: Medline
- NINDS NIH HHS [NS047341-01] Funding Source: Medline
- NATIONAL CENTER FOR RESEARCH RESOURCES [P20RR015576] Funding Source: NIH RePORTER
- NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [R01NS047341] Funding Source: NIH RePORTER
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To identify the intracellular signaling pathways that mediate the pro-survival activity of NMDA receptors (NMDARs), we studied effects of exogenous NMDA on cultured rat cortical and hippocampal neurons that were treated with a phosphatidylinositol-3-kinase (PI3K) inhibitor, LY294002. NMDA at 5 or 10 mu M protected against LY294002-induced apoptosis, suggesting NMDAR-mediated activation of a survival signaling pathway that is PI3K-independent. NR2B-specific NMDAR blockers antagonized anti-apoptotic effects of NMDA, indicating a critical role of NR2B NMDARs in the neuroprotection. NMDA at 10 mu M suppressed LY294002-induced activation of a pro-apoptotic kinase, glycogen synthase kinase 3 beta (GSK3 beta). GSK3 beta activation by LY294002 was associated with decreased levels of inhibitory GSK3 beta phosphorylation at the Ser9 residue. However, NMDA did not prevent the LY294002-mediated decline of phospho-Ser9 levels. In addition, NMDA inhibited cortical neuron apoptosis induced by the overexpression of either wild type (wt) or Ser9Ala mutant form of GSK3 beta, suggesting that NMDA suppressed GSK3 beta in a Ser9-independent manner. Finally, inhibition of NR2B NMDARs reduced the NMDA protection against overexpression of GSK3 beta wt. These data indicate that moderate stimulation of NR2B NMDAR protects against inhibition of PI3K by a Ser9-independent inhibition of the pro-apoptotic activity of GSK3 beta. Hence, the activation of NR2B and the Ser9-independent inhibition of GSK3 beta are two newly identified elements of the signaling network that mediates the pro-survival effects of NMDA.
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