A1 Refereed original research article in a scientific journal

Mechanisms of NOS1AP action on NMDA receptor-nNOS signaling




AuthorsCourtney MJ, Li LL, Lai YY

PublisherFRONTIERS RESEARCH FOUNDATION

Publishing placeSwitzerland

Publication year2014

JournalFrontiers in Cellular Neuroscience

Journal name in sourceFRONTIERS IN CELLULAR NEUROSCIENCE

Journal acronymFRONT CELL NEUROSCI

Article number252

Volume8

Number of pages7

ISSN1662-5102

eISSN1662-5102

DOIhttps://doi.org/10.3389/fncel.2014.00252(external)

Self-archived copy’s web addresshttps://research.utu.fi/converis/portal/detail/Publication/18498644(external)


Abstract
NMDA receptors (NMDAR) are glutamate-gated calcium channels that play pivotal roles in fundamental aspects of neuronal function. Dysregulated receptor function contributes to many disorders. Recruitment by NMDARs of calcium-dependent enzyme nNOS via PSD95 is seen as a key contributor to neuronal dysfunction nNOS adaptor protein (NOS1AP), originally described as a competitor of PSD95:nNOS interaction, is regarded an inhibitor of NMDAR-driven nNOS function. In conditions of NMDAR hyperactivity such as excitotoxicity, one expects NOS1AP to be neuroprotective. Conditions of NMDAR hypoactivity, as thought to occur in schizophrenia, might be exacerbated by NOS1AP. Indeed GWAS have implicated NOS1AP and nNOS in schizophrenia. Several studies now indicate NOS1AP can mediate rather than inhibit NMDAR/nNOS-dependent responses, including excitotoxic signaling. Yet the concept of NOS1AP as an inhibitor of nNOS predominates in studies of human disease genetics. Here we review the experimental evidence to evaluate this apparent controversy, consider whether the known functions of NOS1AP might defend neurons against NMDAR dysregulation and highlight specific areas for future investigation to shed light on the functions of this adaptor protein.

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