DIFFERENTIAL EXPRESSION OF M-CSF, G-CSF, AND GM-CSF BY HUMAN MONOCYTES

被引:65
作者
LEE, MT [1 ]
KAUSHANSKY, K [1 ]
RALPH, P [1 ]
LADNER, MB [1 ]
机构
[1] UNIV WASHINGTON,DIV HEMATOL,SEATTLE,WA 98195
关键词
colony-stimulating factor; gene expression; indomethacin; lipopolysaccharide; mRNA; prostaglandin;
D O I
10.1002/jlb.47.3.275
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The colony-stimulating factors (CSF) belong to a group of proteins which regulate blood cell production. Human monocytes allowed to adhere express high levels of M-CSF transcripts and secreted protein at 24 h in the presence but not in the absence of indomethacin (Indo), an inhibitor of prostaglandin E (PGE) production. When induced with lipopolysaccharide (LPS), adherent monocytes express M-CSF, G-CSF, and GM-CSF transcripts and secrete these proteins and TNF. M-CSF and GM-CSF messages increase in LPS-induced monocytes by the addition of Indo, while G-CSF mRNA appears to decrease. Exogenous addition of PGE-2 to LPS-induced monocytes down-modulates the expression of M-CSF and GM-CSF transcripts. G-CSF message is elevated, suggesting an alternate pathway to G-CSF regulation. PGE-2 inhibits the secretion of CSFs and TNF. In contrast, LPS-induced monocytes held 24 h in nonadherent culture express G- and GM-CSF but not M-CSF. Monocytes that are adhered for 24 h and then treated with LPS for an additional 24 h express only M-CSF message and secrete M-CSF and TNF. PGE-2 added with LPS during the 24-48 h induction blocks M-CSF and TNF production, but appears to enhance M-CSF message expression, in contrast to its effect on 0 h inductions. These results suggest that adherence alone induces M-CSF gene expression, but low levels of PGE or other arachidonic acid metabolites limit this expression. Other events in 1 d-cultured monocytes block the ability to induce G-CSF and GM-CSF expression with LPS, and block the suppressive effect of PGE-2 on M-CSF expression at the RNA level.
引用
收藏
页码:275 / 282
页数:8
相关论文
共 30 条
  • [1] BECKER S, 1987, J IMMUNOL, V139, P3703
  • [2] ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE
    CHIRGWIN, JM
    PRZYBYLA, AE
    MACDONALD, RJ
    RUTTER, WJ
    [J]. BIOCHEMISTRY, 1979, 18 (24) : 5294 - 5299
  • [3] THE HUMAN HEMATOPOIETIC COLONY-STIMULATING FACTORS
    CLARK, SC
    KAMEN, R
    [J]. SCIENCE, 1987, 236 (4806) : 1229 - 1237
  • [4] CREASEY AA, 1986, CANCER RES, V46, P5687
  • [5] DAS SK, 1982, J BIOL CHEM, V257, P13679
  • [6] REGULATION OF THE IMMUNE-RESPONSE BY PROSTAGLANDINS
    GOODWIN, JS
    CEUPPENS, J
    [J]. JOURNAL OF CLINICAL IMMUNOLOGY, 1983, 3 (04) : 295 - 315
  • [7] HASKILL S, 1988, J IMMUNOL, V140, P1690
  • [8] EXPRESSION OF THE MACROPHAGE SPECIFIC COLONY-STIMULATING FACTOR (CSF-1) DURING HUMAN MONOCYTIC DIFFERENTIATION
    HORIGUCHI, J
    WARREN, MK
    RALPH, P
    KUFE, D
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1986, 141 (03) : 924 - 930
  • [9] ISHIZAKA Y, 1986, EXP HEMATOL, V14, P1
  • [10] ROLE OF CARBOHYDRATE IN THE FUNCTION OF HUMAN GRANULOCYTE MACROPHAGE COLONY-STIMULATING FACTOR
    KAUSHANSKY, K
    OHARA, PJ
    HART, CE
    FORSTROM, JW
    HAGEN, FS
    [J]. BIOCHEMISTRY, 1987, 26 (15) : 4861 - 4867