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.
引用
收藏
页码:232 / 236
页数:5
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