CHARACTERIZATION OF SUBSTANCE-P BINDING TO HUMAN MONOCYTES/MACROPHAGES

被引:37
作者
LUCEY, DR
NOVAK, JM
POLONIS, VR
LIU, YL
GARTNER, S
机构
[1] WALTER REED ARMY MED CTR,DEPT RETROVIRAL RES,ROCKVILLE,MD 20850
[2] HENRY M JACKSON FDN,ROCKVILLE,MD 20850
[3] USA,MED RES INST INFECT DIS,DIV BACTERIOL,FT DETRICK,MD 21702
关键词
D O I
10.1128/CDLI.1.3.330-335.1994
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Substance P (SP), a member of the tachykinin family of neuropeptides, can immunomodulate human T cells and monocytes. SP has been shown to stimulate human monocytes to produce inflammatory cytokines and superoxide ions, and it enhances tumoricidal activity in vitro. A specific SP receptor, however, has not been identified on human monocytes/macrophages. In this study, we report that I-125-Sp binds to human monocytes/macrophages with high affinity and specificity (K-d = 2.7 x 10(-8) to 5.5 x 10(-8) M). Our measurements of binding affinity to this single class of receptors were possible only when experiments were performed in the presence of excess serine proteinase inhibitor (serpin) enzyme complex receptor ligand. We determined that I-125-Sp bound to a specific receptor on human monocytes/macrophages and that this binding was detectable as early as 6 h and was maintained throughout 6 to 8 weeks in culture. Modulation of the diverse immunological and inflammatory effects of SP on human monocytes may be mediated through this specific SP receptor.
引用
收藏
页码:330 / 335
页数:6
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