Extracellular ATP triggers cyclic AMP-dependent differentiation of HL-60 cells

被引:40
作者
Jiang, LL [1 ]
Foster, FM [1 ]
Ward, P [1 ]
Tasevski, V [1 ]
Luttrell, BM [1 ]
Conigrave, AD [1 ]
机构
[1] ROYAL N SHORE HOSP,DEPT ENDOCRINOL,ST LEONARDS,NSW 2065,AUSTRALIA
基金
澳大利亚研究理事会;
关键词
D O I
10.1006/bbrc.1997.6345
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
Extracellular ATP and ATP gamma S (1-1000 mu M) stimulated cyclic AMP (cAMP) production in undifferentiated HL-60 cells, The potency order for adenine nucleotides and adenosine was ATP gamma S > ATP much greater than ADP >(3) AMP = Adenosine. Indomethacin (50 mu M) had no effect on ATP-induced cAMP production, ATP and ATP gamma S also suppressed cell growth and induced differentiation as revealed by fMLP-stimulated beta-glucuronidase release 48 h after exposure, The potency order for the induction of fMLP-stimulated beta-glucuronidase release by adenine nucleotides and adenosine was ATP gamma S >(3) ATP > ADP > AMP = Adenosine approximate to 0. The protein kinase A inhibitor Rp-8-Br-cAMPS (10-200 mM) suppressed ATP-induced differentiation but had no effect on ATP-dependent growth suppression, UTP which, libe ATP, activates P-2U receptors on HL-60 cells, had no effect on cAMP production, cell growth, or differentiation. The data suggest the existence of a novel receptor for ATP on undifferentiated HL-60 cells that is coupled to the activation of adenylate cyclase and cAMP-dependent differentiation. (C) 1997 Academic Press.
引用
收藏
页码:626 / 630
页数:5
相关论文
共 33 条
[1]   EPINEPHRINE INDUCES BETA-ADRENERGIC DESENSITIZATION AND DIFFERENTIATION OF HL-60 CELLS [J].
BANG, BE ;
AARBAKKE, J ;
SAGER, G .
SCANDINAVIAN JOURNAL OF CLINICAL & LABORATORY INVESTIGATION, 1993, 53 (04) :311-315
[2]   TERMINAL NEUROENDOCRINE DIFFERENTIATION OF HUMAN PROSTATE CARCINOMA-CELLS IN RESPONSE TO INCREASED INTRACELLULAR CYCLIC-AMP [J].
BANG, YJ ;
PIRNIA, F ;
FANG, WG ;
KANG, WK ;
SARTOR, O ;
WHITESELL, L ;
HA, MJ ;
TSOKOS, M ;
SHEAHAN, MD ;
NGUYEN, P ;
NIKLINSKI, WT ;
MYERS, CE ;
TREPEL, JB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (12) :5330-5334
[3]   P2X(1) receptor activation in HL60 cells [J].
Buell, G ;
Michel, AD ;
Lewis, C ;
Collo, G ;
Humphrey, PPA ;
Surprenant, A .
BLOOD, 1996, 87 (07) :2659-2664
[4]   CYCLIC NUCLEOTIDE-INDUCED MATURATION OF HUMAN PROMYELOCYTIC LEUKEMIA-CELLS [J].
CHAPLINSKI, TJ ;
NIEDEL, JE .
JOURNAL OF CLINICAL INVESTIGATION, 1982, 70 (05) :953-964
[5]  
CHOCHUNG YS, 1990, CANCER RES, V50, P7093
[6]   REVIEW - CA2+-MOBILIZING RECEPTORS FOR ATP AND UTP [J].
CONIGRAVE, AD ;
JIANG, L .
CELL CALCIUM, 1995, 17 (02) :111-119
[7]  
COTE S, 1993, AM J PHYSIOL, V264, pH1498, DOI 10.1152/ajpheart.1993.264.5.H1498
[8]   CHRONIC TREATMENT WITH P2-PURINERGIC RECEPTOR AGONISTS INDUCES PHENOTYPIC MODULATION OF THE HL-60 AND U937 HUMAN MYELOGENOUS LEUKEMIA-CELL LINES [J].
COWEN, DS ;
BERGER, M ;
NUTTLE, L ;
DUBYAK, GR .
JOURNAL OF LEUKOCYTE BIOLOGY, 1991, 50 (02) :109-122
[9]  
DUBYAK GR, 1990, ANN NY ACAD SCI, V603, P227
[10]   ACTIVATION OF CELL-GROWTH INHIBITOR BY ECTOPROTEIN KINASE-MEDIATED PHOSPHORYLATION IN TRANSFORMED MOUSE FIBROBLASTS [J].
FRIEDBERG, I ;
BELZER, I ;
OGEDPLESZ, O ;
KUEBLER, D .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (35) :20560-20567