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
相关论文
共 50 条
  • [41] DNA-REPLICATION AND POLY(ADP-RIBOSYL)ATION OF CHROMATIN
    ANACHKOVA, B
    RUSSEV, G
    POIRIER, GG
    CYTOBIOS, 1989, 59 (236) : 19 - 28
  • [42] MODULATION OF CHROMATIN STRUCTURE BY POLY(ADP-RIBOSYL)ATION - REVIEW
    DEMURCIA, G
    HULETSKY, A
    POIRIER, GG
    BIOCHEMISTRY AND CELL BIOLOGY-BIOCHIMIE ET BIOLOGIE CELLULAIRE, 1988, 66 (06): : 626 - 635
  • [43] CHROMOSOMAL PROTEIN POLY(ADP-RIBOSYL)ATION IN PANCREATIC NUCLEOSOMES
    AUBIN, RJ
    DAM, VT
    MICLETTE, J
    BROUSSEAU, Y
    POIRIER, GG
    CANADIAN JOURNAL OF BIOCHEMISTRY, 1982, 60 (03): : 295 - 305
  • [44] Poly(ADP-ribosyl)ation, genomic instability and mammalian longevity
    Bürkle, A
    Meyer, R
    Rossi, L
    Brabeck, C
    Beneke, S
    Küpper, JH
    Scovassi, AI
    Müller, MM
    MECHANISMS OF AGEING AND DEVELOPMENT, 2002, 123 (04) : 443 - 444
  • [45] Poly(ADP-ribosyl)ation and epigenetics - Is CTCF PARt of the plot?
    Klenova, E
    Ohlsson, R
    CELL CYCLE, 2005, 4 (01) : 96 - 101
  • [46] POLY(ADP-RIBOSYL)ATION REACTIONS AND MODULATION OF CHROMATIN STRUCTURE
    DEMURCIA, G
    GRADWOHL, G
    MAZEN, A
    MENISSIERDEMURCIA, J
    HULETSKY, A
    POIRIER, G
    DNA REPAIR MECHANISMS AND THEIR BIOLOGICAL IMPLICATIONS IN MAMMALIAN CELLS, 1989, 182 : 365 - 377
  • [47] Poly(ADP-ribosyl)ation reactions in the regulation of nuclear functions
    D'Amours, D
    Desnoyers, S
    D'Silva, I
    Poirier, GG
    BIOCHEMICAL JOURNAL, 1999, 342 : 249 - 268
  • [48] Poly(ADP-ribosyl)ation and host-pathogen interactions
    Briggs, A. G.
    Adams-Phillips, L. C.
    Bent, A. F.
    PHYTOPATHOLOGY, 2009, 99 (06) : S16 - S16
  • [49] Role of CTCF poly(ADP-Ribosyl)ation in the regulation of apoptosis in breast cancer cells
    Venkatraman, Bhooma
    Klenova, Elena
    INDIAN JOURNAL OF MEDICAL AND PAEDIATRIC ONCOLOGY, 2015, 36 (01) : 49 - 54
  • [50] Very low concentrations of arsenite suppress poly(adp-ribosyl)ation in mammalian cells
    Hartwig, A
    Pelzer, A
    Asmuss, M
    Bürkle, A
    INTERNATIONAL JOURNAL OF CANCER, 2003, 104 (01) : 1 - 6