Expression of intercellular adhesion molecule-1 on macrophages in vitro as a marker of activation

被引:31
作者
Bernatchez, SF
Atkinson, MR
Parks, PJ
机构
[1] LIFE SCI SECTOR LAB, ST PAUL, MN 55144 USA
[2] ANALYT & PROPERTIES RES LABS, ST PAUL, MN 55144 USA
关键词
macrophages; cytokines; cell surface markers; activation; polylactic acid;
D O I
10.1016/S0142-9612(97)00072-0
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Macrophage activation is a major component of wound healing. It also determines the extent of inflammatory reactions and the response of the body to implanted materials. We have previously shown, using an in vitro model, that the extent of spreading of macrophages on different materials is a marker of activation, and that a soluble inducer has a dose-response effect on the secretion of cytokines in the culture medium. This work investigates the expression of three different cell surface markers [macrophages MAC-1, MAC-3 and intercellular adhesion molecule-1 (ICAM-1)] on macrophages in vitro using confocal microscopy and shows that ICAM-1 is also a marker of macrophage activation in this model. We observed increased amounts of ICAM-1 on activated macrophages compared to unactivated macrophages, whereas MAC-1 and MAC-3 were either expressed constitutively or demonstrated no quantitative change in expression after activation under the same experimental conditions. We also tested the expression of ICAM-1 with various concentrations of soluble inducers (lipopolysaccharide, 0.001, 0.01, 0.1, 1 and 10 mu g ml(-1); S-27609, 0.1, 0.25, 0.5, 1, 2 and 3 mu g ml(-1)) and on a sheet of polylactic acid alone or in combination with soluble inducers. All doses of soluble inducers induced the expression of ICAM-1 on cells grown in glass chamber slides. The induction was not dose related but seemed to work rather in an on-off manner. There was no effect of material on ICAM-1 expression on the cell surface when no soluble inducer was added. This was similar to cytokine secretion, which was not induced by our material alone. When either lipopolysaccharide or S-27609 was used in combination with the material, there was an increase in the average measured intensity of ICAM-1. In this in vitro model, ICAM-1 staining as measured by confocal microscopy is a marker for macrophage activation. Our results suggest that the extent of macrophage activation as measured by ICAM-1 and by cytokine secretion is more sensitive to soluble inducers than to the action of the flat sheet of polylactic acid. (C) 1997 Elsevier Science Limited. All rights reserved.
引用
收藏
页码:1371 / 1378
页数:8
相关论文
共 60 条
[11]   TNF AND IL-1 GENERATION BY HUMAN MONOCYTES IN RESPONSE TO BIOMATERIALS [J].
CARDONA, MA ;
SIMMONS, RL ;
KAPLAN, SS .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 1992, 26 (07) :851-859
[12]  
Chapekar MS, 1996, J BIOMED MATER RES, V31, P251, DOI 10.1002/(SICI)1097-4636(199606)31:2<251::AID-JBM12>3.0.CO
[13]  
2-O
[14]   SURFACE MATRIX BINDING ALTERS MURINE PERITONEAL MONONUCLEAR PHAGOCYTE TNF-ALPHA AND IL-6 INDUCTION [J].
DARVILLE, T ;
TABOR, DR ;
THEUS, SA ;
JACOBS, RF .
IMMUNOLOGICAL INVESTIGATIONS, 1992, 21 (06) :539-552
[15]   BINDING OF THE INTEGRIN MAC-1 (CD11B/CD18) TO THE 3RD IMMUNOGLOBULIN-LIKE DOMAIN OF ICAM-1 (CD54) AND ITS REGULATION BY GLYCOSYLATION [J].
DIAMOND, MS ;
STAUNTON, DE ;
MARLIN, SD ;
SPRINGER, TA .
CELL, 1991, 65 (06) :961-971
[16]   ASBESTOS FIBERS AND SILICA PARTICLES STIMULATE RAT ALVEOLAR MACROPHAGES TO RELEASE TUMOR NECROSIS FACTOR - AUTOREGULATORY ROLE OF LEUKOTRIENE-B4 [J].
DUBOIS, CM ;
BISSONNETTE, E ;
ROLAPLESZCZYNSKI, M .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1989, 139 (05) :1257-1264
[17]  
DUSTIN ML, 1986, J IMMUNOL, V137, P245
[18]   USE OF SURFACE MOLECULES AND RECEPTORS FOR STUDYING MACROPHAGES AND MONONUCLEAR PHAGOCYTES [J].
FRASER, I ;
DOYLE, A ;
HUGHES, D ;
GORDON, S .
JOURNAL OF IMMUNOLOGICAL METHODS, 1994, 174 (1-2) :95-102
[19]  
FRASER I, 1993, BLOOD CELL BIOCH, V5, P1
[20]   MACROPHAGE ACTIVATION BY POLYMERIC NANOPARTICLES OF POLYALKYLCYANOACRYLATES - ACTIVITY AGAINST INTRACELLULAR LEISHMANIA-DONOVANI ASSOCIATED WITH HYDROGEN-PEROXIDE PRODUCTION [J].
GASPAR, R ;
PREAT, V ;
OPPERDOES, FR ;
ROLAND, M .
PHARMACEUTICAL RESEARCH, 1992, 9 (06) :782-787