Ca2+-permeable AMPA receptors are activated under less restrictive conditions than the NMDA receptor, are found in numerous neuron types, and may regulate pathways that are more generally controlled by NMDAR Ca2+ currents. We have shown that Ca2+-permeable AMPARs, like the NMDAR, can activate neuronal nitric oxide synthase (nNOS). In our first Aim we will determine if Ca2+-permeable AMPA receptors can activate successive regulatory phosphorylations of nNOS by Akt and CaMKII, previously shown by us (Rameau et al., 2007) to be induced by the NMDAR. We will study scaffolding structures and biochemical pathways Akt and CaMKII that contribute to nNOS control by Ca2+-permeable AMPARs. GluR2 when modified by RNA editing dominantly blocks the Ca2+ conductance of AMPAR channels. In contrast, unedited GluR2 is highly toxic through its Ca2+ permeability and constitutive trafficking (Mahajan and Ziff, 2007). Recently we have found that NMDAR activity can degrade the GluR2 pre mRNA editing enzyme, ADAR2.
Our second Aim i s to analyze the pathological, NMDAR-dependent proteolytic cleavage of ADAR2, the production of unedited GluR2 as RNA editing activity declines, and the mechanisms by which Ca2+-permeable AMPARs including the unedited GluR2 can kill neurons. To limit Ca2+-toxicity, cells have evolved mechanisms for restricting synaptic AMPAR Ca2+ currents in which Ca2+-impermeable AMPA receptors replace Ca2+-impermeable ones at the synapse. In preliminary studies, we have found that release of Ca2+ from ER stores cooperates with CaMKII to stimulate trafficking of GluR2 from the endoplasmic reticulum to the plasma membrane. In our third Aim, we will study the Ca2+-dependent trafficking of GluR2 from the ER, and distinguish if its control relies on the assembly of GluR2 into tetramers or release of GluR2 from ER retention. We will determine the domains of GluR2 that respond to Ca2+ and the roles of intracellular Ca2+ levels, CaMKII, PICK1 in the export mechanism, including the roles of PICK1-CaMKII complexes. These studies will provide a comprehensive analysis of physiologic and pathologic pathways controlled by Ca2+-permeable AMPARs and mechanisms for regulating Ca2+-permeable AMPAR function.
Health Narrative: This grant is concerned with the physiologic functions of Ca2+ permeable AMPA receptors in brain regulation and synapse plasticity, and the consequences of formation of pathological Ca2+ permeable AMPA receptors, which have been implicated in Amyotrophic Lateral Sclerosis. Finally the grant will study pathways of trafficking of Ca2+-impermeable AMPAR receptors that block the Ca2+ permeable ones, and protect against neuron excitotoxic death.
|Su, Chen; D'amour, James; Lee, Michelle et al. (2015) Persistent pain alters AMPA receptor subunit levels in the nucleus accumbens. Mol Brain 8:46|
|Kim, Seonil; Violette, Caroline J; Ziff, Edward B (2015) Reduction of increased calcineurin activity rescues impaired homeostatic synaptic plasticity in presenilin 1 M146V mutant. Neurobiol Aging 36:3239-46|
|Kim, Seonil; Ziff, Edward B (2014) Calcineurin mediates synaptic scaling via synaptic trafficking of Ca2+-permeable AMPA receptors. PLoS Biol 12:e1001900|
|Peng, Xing-Xiang; Cabeza de Vaca, Soledad; Ziff, Edward B et al. (2014) Involvement of nucleus accumbens AMPA receptor trafficking in augmentation of D- amphetamine reward in food-restricted rats. Psychopharmacology (Berl) 231:3055-63|
|Lu, Wei; Khatri, Latika; Ziff, Edward B (2014) Trafficking of Î±-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor (AMPA) receptor subunit GluA2 from the endoplasmic reticulum is stimulated by a complex containing Ca2+/calmodulin-activated kinase II (CaMKII) and PICK1 protein and by release J Biol Chem 289:19218-30|
|Goffer, Yossef; Xu, Duo; Eberle, Sarah E et al. (2013) Calcium-permeable AMPA receptors in the nucleus accumbens regulate depression-like behaviors in the chronic neuropathic pain state. J Neurosci 33:19034-44|
|Tukey, David S; Lee, Michelle; Xu, Duo et al. (2013) Differential effects of natural rewards and pain on vesicular glutamate transporter expression in the nucleus accumbens. Mol Brain 6:32|
|Tukey, David S; Ferreira, Jainne M; Antoine, Shannon O et al. (2013) Sucrose ingestion induces rapid AMPA receptor trafficking. J Neurosci 33:6123-32|
|Mahajan, S S; Thai, K H; Chen, K et al. (2011) Exposure of neurons to excitotoxic levels of glutamate induces cleavage of the RNA editing enzyme, adenosine deaminase acting on RNA 2, and loss of GLUR2 editing. Neuroscience 189:305-15|