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Cell Death Dis ; 9(5): 449, 2018 05 01.
Article in English | MEDLINE | ID: mdl-29670079

ABSTRACT

The role of astrocyte elevated gene-1 (AEG-1) in nigral dopaminergic (DA) neurons has not been studied. Here we report that the expression of AEG-1 was significantly lower in DA neurons in the postmortem substantia nigra of patients with Parkinson's disease (PD) compared to age-matched controls. Similarly, decreased AEG-1 levels were found in the 6-hydroxydopamine (6-OHDA) mouse model of PD. An adeno-associated virus-induced increase in the expression of AEG-1 attenuated the 6-OHDA-triggered apoptotic death of nigral DA neurons. Moreover, the neuroprotection conferred by the AEG-1 upregulation significantly intensified the neurorestorative effects of the constitutively active ras homolog enriched in the brain [Rheb(S16H)]. Collectively, these results demonstrated that the sustained level of AEG-1 as an important anti-apoptotic factor in nigral DA neurons might potentiate the therapeutic effects of treatments, such as Rheb(S16H) administration, on the degeneration of the DA pathway that characterizes PD.


Subject(s)
Apoptosis , Astrocytes/metabolism , Dopaminergic Neurons/metabolism , Membrane Glycoproteins/biosynthesis , Substantia Nigra/metabolism , Up-Regulation , Animals , Astrocytes/pathology , Disease Models, Animal , Dopaminergic Neurons/pathology , Humans , Membrane Glycoproteins/genetics , Mice , Oxidopamine/adverse effects , Oxidopamine/pharmacology , Parkinson Disease, Secondary/chemically induced , Parkinson Disease, Secondary/genetics , Parkinson Disease, Secondary/metabolism , Parkinson Disease, Secondary/pathology , Ras Homolog Enriched in Brain Protein/genetics , Ras Homolog Enriched in Brain Protein/metabolism , Substantia Nigra/pathology
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