4.3 Article

D-Amino acid oxidase knockdown in the mouse cerebellum reduces NR2A mRNA

Journal

MOLECULAR AND CELLULAR NEUROSCIENCE
Volume 46, Issue 1, Pages 167-175

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.mcn.2010.08.018

Keywords

Lentivirus; D-Amino acid oxidase; RNA-interference; Cerebellum; NMDA receptor; shRNA; c6 glioma; Western blot

Categories

Funding

  1. Biotechnology, Biological Sciences Research Council (BBSRC), UK
  2. BBSRC [BB/I006311/1, BB/D017912/1] Funding Source: UKRI
  3. MRC [G0500822, G0801352] Funding Source: UKRI
  4. Biotechnology and Biological Sciences Research Council [BB/D017912/1, BB/I006311/1] Funding Source: researchfish
  5. Medical Research Council [G0801352, G0500822] Funding Source: researchfish

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Virus mediated RNA-interference (RNAi) is a powerful approach to study genes in vivo. Here we report a method using lentivirus-delivered RNAi to knockdown the glial enzyme, is-amino acid oxidase (DAD), in the mouse cerebellum. After initial characterisation in vitro, we achieved a 40-50% reduction of DAD mRNA in the cerebellum 7 and 28 days after a single injection of lentivirus encoding a DAO-specific, short-hairpin RNA. Injections also decreased DAO immunoreactivity (-33%). The major substrate for DAD is D-serine, an N-methyl-D-aspartate receptor (NMDAR) co-agonist. Thus, we also measured whether DAD knockdown impacted on D-serine, or expression of NMDAR subunits, and found that DAD RNAi led to increased cerebellar D-serine levels (+77%), and decreased NMDAR subunit NR2A mRNA (-22%), but did not affect NR1 or NR2C mRNAs. These data demonstrate the utility of lentiviruses to deliver RNAi to glial cells within the cerebellum, and confirm the role of DAO in D-serine metabolism. They also provide a tool to investigate DAO, an enzyme currently of considerable interest in the pathophysiology and therapy of schizophrenia. (C) 2010 Elsevier Inc. All rights reserved.

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