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The Journal of Neuroscience, April 22, 2009, 29(16):5260-5265; doi:10.1523/JNEUROSCI.1067-09.2009

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Brief Communications
Neuroprotection by the NR3A Subunit of the NMDA Receptor

Nobuki Nakanishi,^1 * Shichun Tu,^1 * Yeonsook Shin,^1,2 Jiankun Cui,¹ Toru Kurokawa,¹ Dongxian Zhang,¹ H.-S. Vincent Chen,^1,4 Gary Tong,^1,3 and Stuart A. Lipton^1,3

¹Center for Neuroscience, Aging, and Stem Cell Research, Burnham Institute for Medical Research, La Jolla, California 92037, ²Department of Molecular Pharmacology, Kanazawa University Graduate School of Medicine, Kanazawa, Ishikawa 920-8640, Japan, ³Department of Neurosciences, University of California, San Diego, La Jolla, California 92093, and ⁴Division of Cardiology, University of California, San Diego, La Jolla, California 92037

Correspondence should be addressed to Nobuki Nakanishi at the above address. Email: nnakanishi{at}burnham.org

Hyperactivation of NMDA-type glutamate receptors (NMDARs) results in excitotoxicity, contributing to damage in stroke and neurodegenerative disorders. NMDARs are generally comprised of NR1/NR2 subunits but may contain modulatory NR3 subunits. Inclusion of NR3 subunits reduces the amplitude and dramatically decreases the Ca²⁺ permeability of NMDAR-associated channels in heterologous expression systems and in transgenic mice. Since excessive Ca²⁺ influx into neurons is a crucial step for excitotoxicity, we asked whether NR3A subunits are neuroprotective. To address this question, we subjected neurons genetically lacking NR3A to various forms of excitotoxic insult. We found that cultured neurons prepared from NR3A knock-out (KO) mice displayed greater sensitivity to damage by NMDA application than wild-type (WT) neurons. In vivo, neonatal, but not adult, WT mice contain NR3A in the cortex, and neonatal NR3A KO mice manifested more damage than WT after hypoxia–ischemia. In adult retina, one location where high levels of NR3A normally persist into adulthood, injection of NMDA into the eye killed more retinal ganglion cells in adult NR3A KO than WT mice. These data suggest that endogenous NR3A is neuroprotective. We next asked whether we could decrease excitotoxicity by overexpressing NR3A. We found that cultured neurons expressing transgenic (TG) NR3A displayed greater resistance to NMDA-mediated neurotoxicity than WT neurons. Similarly in vivo, adult NR3A TG mice subjected to focal cerebral ischemia manifested less damage than WT mice. These data suggest that endogenous NR3A protects neurons, and exogenously added NR3A increases neuroprotection and could be potentially exploited as a therapeutic.

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Received March 4, 2009; accepted March 24, 2009.

Correspondence should be addressed to Nobuki Nakanishi at the above address. Email: nnakanishi{at}burnham.org

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