A SPECIFIC SEQUENCE OF STIMULATION IS REQUIRED TO INDUCE SYNTHESIS OF THE ANTIMICROBIAL MOLECULE NITRIC-OXIDE BY MOUSE MACROPHAGES

被引:64
作者
LORSBACH, RB
RUSSELL, SW
机构
[1] UNIV KANSAS,MED CTR,CTR CANC,WILKINSON LAB,KANSAS CITY,KS 66160
[2] UNIV KANSAS,MED CTR,DEPT PATHOL,KANSAS CITY,KS 66160
[3] UNIV KANSAS,MED CTR,DEPT ONCOL,KANSAS CITY,KS 66160
[4] UNIV KANSAS,MED CTR,DEPT MICROBIOL MOLEC GENET & IMMUNOL,KANSAS CITY,KS 66160
关键词
D O I
10.1128/IAI.60.5.2133-2135.1992
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Nitric oxide production by macrophages required either simultaneous or sequential exposure to gamma interferon and lipopolysaccharide; exposure to lipopolysaccharide followed by exposure to gamma interferon gave little response. The apparently evanescent nature of the lipopolysaccharide signal, necessitating persistent stimulation, could be essential to down-regulating nitric oxide production after bacteria are cleared in vivo.
引用
收藏
页码:2133 / 2135
页数:3
相关论文
共 18 条
  • [1] ADAMS LB, 1991, J IMMUNOL, V147, P1642
  • [2] DING AH, 1988, J IMMUNOL, V141, P2407
  • [3] GREEN SJ, 1990, J IMMUNOL, V145, P4290
  • [4] GREEN SJ, 1990, J IMMUNOL, V144, P278
  • [5] NITRIC-OXIDE - A CYTO-TOXIC ACTIVATED MACROPHAGE EFFECTOR MOLECULE
    HIBBS, JB
    TAINTOR, RR
    VAVRIN, Z
    RACHLIN, EM
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1988, 157 (01) : 87 - 94
  • [6] HIGUCHI M, 1990, J IMMUNOL, V144, P1425
  • [7] HOGAN MM, 1988, J IMMUNOL, V140, P513
  • [8] KELLER R, 1990, CANCER RES, V50, P1421
  • [9] LEUNG KP, 1985, CELL TISSUE RES, V239, P693
  • [10] LEVIN J, 1970, J LAB CLIN MED, V75, P903