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PMID: 10568510 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Synuclein expression is decreased in rat substantia nigra following induction of apoptosis by intrastriatal 6-hydroxydopamine.

Neuroscience letters ·Vol. 275 ·No. 2 ·1999-11-12 ·Pages 105-8

Kholodilov NG, Oo TF, Burke RE

Abstract

We have previously shown that synuclein is upregulated in the substantia nigra following developmental lesion of the target striatum. In this model, synuclein is preferentially expressed in normal-appearing neurons, rather than those which undergo apoptosis. It has been proposed, however, that synuclein may mediate apoptosis in other contexts, such as that induced by neurotoxins. To examine this possibility, we have studied a model in which apoptosis is induced in dopamine neurons by intrastriatal injection of 6-hydroxydopamine. In this model synuclein mRNA and protein expression are not upregulated at any time point, but instead diminish as dopamine neurons die. We observe a complete dissociation between apoptotic morphology and synuclein protein expression. We conclude that synuclein is unlikely to play a direct role in apoptotic death in dopamine neurons and is more likely, in the target injury model, to play a role in protection or restoration of neurons which survive.

MeSH Terms
Animals Apoptosis/drug effects Blotting, Northern Corpus Striatum/drug effects Immunohistochemistry Nerve Tissue Proteins/metabolism Neurons/metabolism Oxidopamine/pharmacology RNA, Messenger/metabolism Rats Substantia Nigra/metabolism,pathology Synucleins
Chemicals
Nerve Tissue Proteins RNA, Messenger Synucleins Oxidopamine
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Kholodilov N G
Department of Neurology, Columbia University, The College of Physicians and Surgeons, New York, NY 10032, USA.
Oo T F
Burke R E
Article Info
Journal
Neuroscience letters
Abbr.
Neurosci Lett
ISSN
0304-3940
Published
1999-11-12
Pages
105-8
Language
English
Region
Ireland
NLM ID
7600130
Subset
IM
Grants
NINDS NIH HHS · NS26836 · United States
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