Resveratrol induces Fas signalling-independent apoptosis in THP-1 human monocytic leukaemia cells

被引:86
作者
Tsan, MF
White, JE
Maheshwari, JG
Bremner, TA
Sacco, J
机构
[1] Stratton VA Med Ctr, Res Serv 151, Albany, NY 12208 USA
[2] Stratton VA Med Ctr, Med Serv, Albany, NY 12208 USA
[3] Albany Med Coll, Dept Med, Albany, NY 12208 USA
[4] Albany Med Coll, Dept Physiol & Cell Biol, Albany, NY 12208 USA
[5] Howard Univ, Dept Biol, Washington, DC 20059 USA
关键词
resveratrol; apoptosis; monocytic leukaemia; Fas receptor; Fas ligand;
D O I
10.1046/j.1365-2141.2000.01980.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Rosveratrol, a natural product present in wine, has recently been shown to inhibit the growth of a number of cancer cell lines in vitro, In the current study, we have demonstrated that resveratrol inhibits the growth of THP-1 human monocytic leukaemia cells in a dose-dependent manner with a median effective dose of 12 mu M. It did not induce differentiation of THP-1 cells and had no toxic effect on THP-1 cells that had been induced to differentiate into monocytcs/macrophagcs by phorbol myristate acetate, A significant fraction of resveratrol-treated cells underwent apoptosis as judged by flow cytometric analysis of DNA content, DNA fragmentation and caspase-specific cleavage of poly(ADP-ribosyl) polymerase. Resveratrol treatment had no effect on the expression of Fas receptor or Fas ligand (FasL) in THP-1 cells, nor did it induce clustering of Fas receptors, In addition, THP-1 cells were resistant to activating anti-Fas antibody, and neutralizing anti-Fas and/or anti-FasL antibodies had no protective effect against resveratrol-induced inhibition of THP-1 cell growth. The effect of resveratrol on THP-1 cells was reversible after its removal from the culture medium. These results suggest that (1) resveratrol inhibits the growth of THP-1 cells, at least in part, by inducing apoptosis, (2) resveratrol-induced apoptosis of THP-1 cells is independent of the Fas/FasL signalling pathway and (3) resveratrol does not induce differentation of THP-1 cells and has no toxic effect on differentiated THP-1 cells. Thus, resveratrol may be a potential chemotherapeutic agent for the control of acute monocytic leukaemia.
引用
收藏
页码:405 / 412
页数:8
相关论文
共 32 条
[1]   THE HUMAN LEUKEMIA-CELL LINE, THP-1 - A MULTIFACETED MODEL FOR THE STUDY OF MONOCYTE-MACROPHAGE DIFFERENTIATION [J].
AUWERX, J .
EXPERIENTIA, 1991, 47 (01) :22-31
[2]   Resveratrol inhibits metal ion-dependent and independent peroxidation of porcine low-density lipoproteins [J].
Belguendouz, L ;
Fremont, L ;
Linard, A .
BIOCHEMICAL PHARMACOLOGY, 1997, 53 (09) :1347-1355
[3]   THP-1 monocytic leukemia cells express Fas ligand constitutively and kill Fas-positive Jurkat cells [J].
Bremner, TA ;
Chatterjee, D ;
Han, ZY ;
Tsan, MF ;
Wyche, JH .
LEUKEMIA RESEARCH, 1999, 23 (10) :865-870
[4]  
Clément MV, 1998, BLOOD, V92, P996
[5]  
DARZYNKIEWICZ Z, 1994, METHOD CELL BIOL, V41, P15
[6]   Resveratrol arrests the cell division cycle at S/G2 phase transition [J].
Della Ragione, F ;
Cucciolla, V ;
Borriello, A ;
Della Pietra, V ;
Racioppi, L ;
Soldati, G ;
Manna, C ;
Galletti, P ;
Zappia, V .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 250 (01) :53-58
[7]   Expression and function of CD95 (FAS/APO-1) in leukaemia-lymphoma tumour lines [J].
Dirks, W ;
Schone, S ;
Uphoff, C ;
Quentmeier, H ;
Pradella, S ;
Drexler, HG .
BRITISH JOURNAL OF HAEMATOLOGY, 1997, 96 (03) :584-593
[8]   INHIBITION OF HUMAN LDL OXIDATION BY RESVERATROL [J].
FRANKEL, EN ;
WATERHOUSE, AL ;
KINSELLA, JE .
LANCET, 1993, 341 (8852) :1103-1104
[9]   Involvement of the CD95 (APO-1/Fas) receptor/ligand system in drug-induced apoptosis in leukemia cells [J].
Friesen, C ;
Herr, I ;
Krammer, PH ;
Debatin, KM .
NATURE MEDICINE, 1996, 2 (05) :574-577
[10]   MODERATE ALCOHOL INTAKE, INCREASED LEVELS OF HIGH-DENSITY-LIPOPROTEIN AND ITS SUBFRACTIONS, AND DECREASED RISK OF MYOCARDIAL-INFARCTION [J].
GAZIANO, JM ;
BURING, JE ;
BRESLOW, JL ;
GOLDHABER, SZ ;
ROSNER, B ;
VANDENBURGH, M ;
WILLETT, W ;
HENNEKENS, CH .
NEW ENGLAND JOURNAL OF MEDICINE, 1993, 329 (25) :1829-1834