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Cell Death Dis ; 4: e579, 2013 Apr 04.
Article in English | MEDLINE | ID: mdl-23559013

ABSTRACT

The p75 neurotrophin receptor (p75(NTR)) is a known mediator of ß-amyloid (Aß)-induced neurotoxicity implicated in Alzheimer's disease (AD). Here, we demonstrate that death receptor 6 (DR6) binds to p75(NTR) and is a component of the p75(NTR) signaling complex responsible for Aß-induced cortical neuron death. Cortical neurons isolated from either DR6 or p75(NTR) null mice are resistant to Aß-induced neurotoxicity. Blocking DR6 function in cortical neurons by anti-DR6 antibodies that block the binding of DR6 to p75(NTR) receptor complex or by a dominant negative DR6 construct lacking the cytoplasmic signaling death domain attenuates Aß-induced caspase 3 activation and cell death. DR6 expression is upregulated in AD cortex and correlates with elevated neuronal death. Targeting the disruption of the DR6/p75(NTR) complex to prevent Aß cytotoxicity represents a new approach for the treatment of neurodegenerative disorders such as AD.


Subject(s)
Cerebral Cortex/drug effects , Neurons/drug effects , Receptors, Nerve Growth Factor/genetics , Receptors, Tumor Necrosis Factor/genetics , Amyloid beta-Peptides/pharmacology , Animals , Antibodies/pharmacology , Caspase 3/genetics , Caspase 3/metabolism , Cell Death/drug effects , Cerebral Cortex/metabolism , Cerebral Cortex/pathology , Gene Expression Regulation/drug effects , Mice , Mice, Knockout , Neurons/metabolism , Neurons/pathology , Primary Cell Culture , Protein Binding , Receptors, Nerve Growth Factor/deficiency , Receptors, Tumor Necrosis Factor/deficiency , Signal Transduction/drug effects
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