Literature DB >> 9518673

Reduced MK801 binding in neocortical neurons after AAV-mediated transfections with NMDA-R1 antisense cDNA.

D R Shafron1, C E Simpkins, B Jebelli, A L Day, E M Meyer.   

Abstract

Two adeno-associated virus (AAV)-derived plasmids were constructed with portions of the N-methyl-d-aspartic acid-R1 (NMDA-R1) receptor subunit downstream from the AAV p40-(pJDT95dlk-aR1) or cytomegalovirus (CMV) promoter (pTRUF3-aR1) in an antisense orientation. Each plasmid drove expression of antisense NMDA-R1 in primary rat neocortical neuronal cultures 4 days after transfection as detected by reverse transcriptase-polymerase chain reaction (RT-PCR). Transfection with pTRUF3-aR1 (2x4 microgram) but not with pJDT95dlk-aR1 decreased neuronal [3H]MK-801 binding in a dose-dependent manner. Copyright 1998 Elsevier Science B.V.

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Year:  1998        PMID: 9518673     DOI: 10.1016/s0006-8993(97)01029-9

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  1 in total

1.  Therapeutic liabilities of in vivo viral vector tropism: adeno-associated virus vectors, NMDAR1 antisense, and focal seizure sensitivity.

Authors:  Rebecca Haberman; Hugh Criswell; Stephen Snowdy; Zhen Ming; George Breese; R Samulski; Thomas McCown
Journal:  Mol Ther       Date:  2002-10       Impact factor: 11.454

  1 in total

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