SIRT1 deficiency attenuates MPP+-induced apoptosis in dopaminergic cells.
FEBS Lett. 2011 Jan 03; 585(1):219-24.FL

Abstract

One of the functions mediated by sirtuin 1 (SIRT1), the NAD(+)-dependent protein deacetylase, has been suggested to be neuroprotective since resveratrol, a SIRT1 activator, inhibits 1-methyl-4-phenylpyridinium ion (MPP(+))-induced cytotoxicity. In this study, we show that SIRT1 siRNA transfection blocks MPP(+)-induced apoptosis in SH-SY5Y cells. The ratio of potential pro-apoptotic BNIP2 to antiapoptotic BCL-xL was attenuated in SIRT1-deficient cells following MPP(+) treatment. In addition, BNIP2 shRNA-transfected cells showed reduced cleavage of PARP-1, while BNIP2 overexpression intensified the cleavage in MPP(+)-treated SH-SY5Y cells, suggesting that BNIP2 participates in the MPP(+)-induced apoptosis. Overall, these data imply that SIRT1 may mediate MPP(+)-induced cytotoxicity, possibly through the regulation of BNIP2.

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Authors+Show Affiliations

Park G
Department of Pharmacology, School of Medicine, Kyung Hee University, Seoul, Republic of Korea.
Jeong JW
No affiliation info available
Kim JE
No affiliation info available

MeSH

1-Methyl-4-phenylpyridiniumApoptosisApoptosis Regulatory ProteinsBlotting, WesternCarrier ProteinsCell Line, TumorCell SurvivalDopamineDose-Response Relationship, DrugDown-RegulationHumansNeuroblastomaPoly (ADP-Ribose) Polymerase-1Poly(ADP-ribose) PolymerasesRNA InterferenceSirtuin 1

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

21130087