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Neuron ; 49(5): 719-33, 2006 Mar 02.
Article in English | MEDLINE | ID: mdl-16504947

ABSTRACT

ADAR2 is a nuclear enzyme essential for GluR2 pre-mRNA editing at Q/R site-607, which gates Ca2+ entry through AMPA receptor channels. Here, we show that forebrain ischemia in adult rats selectively reduces expression of ADAR2 enzyme and, hence, disrupts RNA Q/R site editing of GluR2 subunit in vulnerable neurons. Recovery of GluR2 Q/R site editing by expression of exogenous ADAR2b gene or a constitutively active CREB, VP16-CREB, which induces expression of endogenous ADAR2, protects vulnerable neurons in the rat hippocampus from forebrain ischemic insult. Generation of a stable ADAR2 gene silencing by delivering small interfering RNA (siRNA) inhibits GluR2 Q/R site editing, leading to degeneration of ischemia-insensitive neurons. Direct introduction of the Q/R site edited GluR2 gene, GluR2(R607), rescues ADAR2 degeneration. Thus, ADAR2-dependent GluR2 Q/R site editing determines vulnerability of neurons in the rat hippocampus to forebrain ischemia.


Subject(s)
Adenosine Deaminase/metabolism , Ischemic Attack, Transient/pathology , Neurons/cytology , Prosencephalon/cytology , RNA Editing/physiology , Receptors, AMPA/metabolism , Animals , Animals, Newborn , Blotting, Northern/methods , Blotting, Western/methods , CREB-Binding Protein/metabolism , Calcium/metabolism , Cell Count/methods , Cell Survival/physiology , Cells, Cultured , Disease Models, Animal , Electric Stimulation/methods , Gene Expression/drug effects , Gene Expression/physiology , Green Fluorescent Proteins/metabolism , Hippocampus/cytology , Immunohistochemistry/methods , In Vitro Techniques , Membrane Potentials/drug effects , Membrane Potentials/physiology , Membrane Potentials/radiation effects , Neurons/metabolism , Phosphopyruvate Hydratase/metabolism , RNA, Messenger/biosynthesis , RNA, Small Interfering/pharmacology , RNA-Binding Proteins , Rats , Reverse Transcriptase Polymerase Chain Reaction/methods
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