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PMID: 16135078 Published · ppublish English Comparative Study Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

CHOP/GADD153 is a mediator of apoptotic death in substantia nigra dopamine neurons in an in vivo neurotoxin model of parkinsonism.

Journal of neurochemistry ·Vol. 95 ·No. 4 ·2005-11-00 ·Pages 974-86

Silva RM, Ries V, Oo TF, Yarygina O, Jackson-Lewis V, Ryu EJ, Lu PD, Marciniak SJ, Ron D, Przedborski S, Kholodilov N, Greene LA, Burke RE

Abstract

There is increasing evidence that neuron death in neurodegenerative diseases, such as Parkinson's disease, is due to the activation of programmed cell death. However, the upstream mediators of cell death remain largely unknown. One approach to the identification of upstream mediators is to perform gene expression analysis in disease models. Such analyses, performed in tissue culture models induced by neurotoxins, have identified up-regulation of CHOP/GADD153, a transcription factor implicated in apoptosis due to endoplasmic reticulum stress or oxidative injury. To evaluate the disease-related significance of these findings, we have examined the expression of CHOP/GADD153 in neurotoxin models of parkinsonism in living animals. Nuclear expression of CHOP protein is observed in developmental and adult models of dopamine neuron death induced by intrastriatal injection of 6-hydroxydopamine (6OHDA) and in models induced by 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP). CHOP is a mediator of neuron death in the adult 60HDA model because a null mutation results in a reduction in apoptosis. In the chronic MPTP model, however, while CHOP is robustly expressed, the null mutation does not protect from the loss of neurons. We conclude that the role of CHOP depends on the nature of the toxic stimulus. For 6OHDA, an oxidative metabolite of dopamine, it is a mediator of apoptotic death.

MeSH Terms
1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine/adverse effects Animals Animals, Newborn Apoptosis/drug effects,physiology Axotomy/methods Behavior, Animal Blotting, Northern/methods Blotting, Western/methods Cell Count/methods DNA-Binding Proteins/genetics,metabolism Disease Models, Animal Dopamine/metabolism Female Gene Expression Regulation/drug effects,physiology Immunohistochemistry/methods In Situ Hybridization/methods Male Mice Mice, Inbred C57BL Mice, Knockout Mutation/physiology Neurons/drug effects,metabolism,pathology Neurotoxins Oxidopamine/toxicity Parkinsonian Disorders/etiology,metabolism,pathology Pregnancy RNA, Messenger/genetics,metabolism Rats Regulatory Factor X Transcription Factors Reverse Transcriptase Polymerase Chain Reaction/methods Substantia Nigra/growth & development,pathology Time Factors Transcription Factor CHOP/deficiency,metabolism Transcription Factors/genetics,metabolism Tyrosine 3-Monooxygenase/metabolism
Chemicals
DNA-Binding Proteins Neurotoxins RNA, Messenger Regulatory Factor X Transcription Factors Transcription Factors Transcription Factor CHOP Oxidopamine 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine Tyrosine 3-Monooxygenase Dopamine
Authors & Affiliations
13 authors, click to expand affiliations / ORCID
Silva Robert M
Department of Neurology, The College of Physicians and Surgeons, Columbia University, New York 10032, USA. [email protected]
Ries Vincent
Oo Tinmarla Frances
Yarygina Olga
Jackson-Lewis Vernice
Ryu Elizabeth J
Lu Phoebe D
Marciniak Stefan J
Ron David
Przedborski Serge
Kholodilov Nikolai
Greene Lloyd A
Burke Robert E
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Article Info
Journal
Journal of neurochemistry
Abbr.
J Neurochem
ISSN
0022-3042
Published
2005-11-00
Epub
2005-00-31
Pages
974-86
Language
English
Region
England
NLM ID
2985190R
PMCID
PMC3082498
Subset
IM
Grants
NINDS NIH HHS · R56 NS026836 · United States
NINDS NIH HHS · R21 NS043628 · United States
NINDS NIH HHS · P50 NS038370 · United States
NINDS NIH HHS · R01 NS026836-14 · United States
NIEHS NIH HHS · R01 ES008681 · United States
NIEHS NIH HHS · ES08681 · United States
NINDS NIH HHS · NS38370 · United States
NINDS NIH HHS · R01 NS026836-13 · United States
NINDS NIH HHS · NS43628 · United States
NINDS NIH HHS · R01 NS026836 · United States
NINDS NIH HHS · P50 NS038370-07 · United States
NINDS NIH HHS · NS26836 · United States
NINDS NIH HHS · P50 NS038370-06 · United States
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