HUMAN PAF RECEPTOR GENE-EXPRESSION - INDUCTION DURING HL-60 CELL-DIFFERENTIATION

被引:44
作者
MULLER, E
DUPUIS, G
TURCOTTE, S
ROLAPLESZCZYNSKI, M
机构
[1] UNIV SHERBROOKE,FAC MED,DIV IMMUNOL,SHERBROOKE J1H 5N4,QUEBEC,CANADA
[2] UNIV SHERBROOKE,FAC MED,DEPT BIOCHEM,SHERBROOKE J1H 5N4,QUEBEC,CANADA
基金
英国医学研究理事会;
关键词
D O I
10.1016/0006-291X(91)92119-5
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
Platelet-activating factor is a potent lipid mediator of inflammation and immune regulation. Its numerous biological activities are mediated through specific receptors on the plasma membranes of responsive cells. The expression of such receptors may be modulated by various agents, including those responsible for cell differentiation. Here, we demonstrate that differentiation of the human promyelocytic leukemia cell line HL-60 by 1α,25(OH)2 vitamin D3 towards the macrophage phenotype is associated with induction of PAF receptor gene expression: PAF receptor mRNA accumulation correlates with the induction and development of specific PAF responsiveness as assayed by [Ca2+]i fluxes. Our studies suggest that PAF responsiveness parallels macrophage differentiation and that PAF receptor expression can be regulated at the transcriptional level. © 1991.
引用
收藏
页码:1580 / 1586
页数:7
相关论文
共 17 条
[11]   EVIDENCE FOR 2 PLATELET ACTIVATING FACTOR RECEPTORS ON EOSINOPHILS - DISSOCIATION BETWEEN PAF-INDUCED INTRACELLULAR CALCIUM MOBILIZATION DE-GRANULATION AND SUPEROXIDES ANION GENERATION IN EOSINOPHILS [J].
KROEGEL, C ;
YUKAWA, T ;
WESTWICK, J ;
BARNES, PJ .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1989, 162 (01) :511-521
[12]  
MURPHY PM, 1990, J IMMUNOL, V145, P2227
[13]  
POUBELLE PE, 1991, IMMUNOLOGY, V72, P181
[14]   REGULATION OF MYC GENE-EXPRESSION IN HL-60 LEUKEMIA-CELLS BY A VITAMIN-D METABOLITE [J].
REITSMA, PH ;
ROTHBERG, PG ;
ASTRIN, SM ;
TRIAL, J ;
BARSHAVIT, Z ;
HALL, A ;
TEITELBAUM, SL ;
KAHN, AJ .
NATURE, 1983, 306 (5942) :492-494
[15]  
ROLAPLESZCZYNSK.M, 1992, IN PRESS J LEUKOCYTE
[16]   THE USE OF HEPARIN AS A SIMPLE COST-EFFECTIVE MEANS OF CONTROLLING BACKGROUND IN NUCLEIC-ACID HYBRIDIZATION PROCEDURES [J].
SINGH, L ;
JONES, KW .
NUCLEIC ACIDS RESEARCH, 1984, 12 (14) :5627-5638
[17]  
VALLARI DS, 1990, J BIOL CHEM, V265, P4261