Literature DB >> 7909752

Expression of NMDAR1-1a (N598Q)/NMDAR2A receptors results in decreased cell mortality.

M Cik1, P L Chazot, F A Stephenson.   

Abstract

Transient expression of wild-type N-methyl-D-aspartate, NMDAR1-1a/NMDAR2A heteromeric receptors, in mammalian cells yields cell death which was prevented by the inclusion of NMDA receptor antagonists in the cell culture media post-transfection. Transient expression of mutant NMDAR1-1a (N598Q)/NMDAR2A receptors resulted in a significant decrease in the percentage of cell death post-transfection. This mutation has been shown to reduce the Ca2+ permeability of cloned NMDA receptors. Thus these results provide indirect evidence for cell death via an NMDA receptor, Ca(2+)-mediated mechanism.

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Year:  1994        PMID: 7909752     DOI: 10.1016/0922-4106(94)90146-5

Source DB:  PubMed          Journal:  Eur J Pharmacol        ISSN: 0014-2999            Impact factor:   4.432


  4 in total

1.  Effects of ethanol on phosphorylation site mutants of recombinant N-methyl-D-aspartate receptors.

Authors:  Minfu Xu; Corigan Thetford Smothers; John J Woodward
Journal:  Alcohol       Date:  2010-12-15       Impact factor: 2.405

2.  Ethanol inhibition of recombinant NMDA receptors is not altered by coexpression of CaMKII-alpha or CaMKII-beta.

Authors:  Minfu Xu; L Judson Chandler; John J Woodward
Journal:  Alcohol       Date:  2008-06-17       Impact factor: 2.405

3.  Dephosphorylation of GluN2B C-terminal tyrosine residues does not contribute to acute ethanol inhibition of recombinant NMDA receptors.

Authors:  Benjamin A Hughes; C Thetford Smothers; John J Woodward
Journal:  Alcohol       Date:  2013-01-26       Impact factor: 2.405

4.  Enhanced ethanol inhibition of recombinant N-methyl-D-aspartate receptors by magnesium: role of NR3A subunits.

Authors:  Chun Jin; C Thetford Smothers; John J Woodward
Journal:  Alcohol Clin Exp Res       Date:  2008-04-26       Impact factor: 3.455

  4 in total

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