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Rapamycin inhibits poly(ADP-ribosyl)ation in intact cells
被引:4
|作者:
Fahrer, Joerg
[1
]
Wagner, Silvia
[2
]
Buerkle, Alexander
[1
]
Koenigsrainer, Alfred
[2
]
机构:
[1] Univ Konstanz, Dept Biol, Mol Toxicol Grp, D-7750 Constance, Germany
[2] Univ Tubingen Hosp, Clin Gen Visceral & Transplantat Surg, ZMF, Tubingen, Germany
关键词:
Rapamycin;
mTOR;
Poly(ADP-ribosyl)ation;
PARP inhibitor;
Fibroblasts;
POLYMERASE;
BINDING;
GROWTH;
DEATH;
PHOSPHORYLATION;
PROTEINS;
TARGET;
MTOR;
D O I:
10.1016/j.bbrc.2009.06.022
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Rapamycin is an immunosuppressive drug, which inhibits the mammalian target of rapamycin (mTOR) kinase activity inducing changes in cell proliferation. Synthesis of poly(ADP-ribose) (PAR) is an immediate cellular response to genotoxic stress catalyzed mostly by poly(ADP-ribose) polymerase 1 (PARP-1), which is also controlled by signaling pathways. Therefore, we investigated whether rapamycin affects PAR production. Strikingly, rapamycin inhibited PAR synthesis in living fibroblasts in a dose-dependent manner as monitored by immunofluorescence. PARP-1 activity was then assayed in vitro, revealing that down-regulation of cellular PAR production by rapamycin was apparently not due to competitive PARP-1 inhibition. Further studies showed that rapamycin did not influence the cellular NAD pool and the activation of PARP-1 in extracts of pretreated fibroblasts. Collectively, our data suggest that inhibition of cellular PAR synthesis by rapamycin is mediated by formation of a detergent-sensitive complex in living cells, and that rapamycin may have a potential as therapeutic PARP inhibitor. (C) 2009 Elsevier Inc. All rights reserved.
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页码:232 / 236
页数:5
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