ENDOTOXIN-REFRACTORY LIVER MACROPHAGES SECRETE TUMOR-NECROSIS-FACTOR-ALPHA UPON VIRAL-INFECTION

被引:9
作者
BUSAM, KJ
SCHULZESPECKING, A
DECKER, K
机构
来源
BIOLOGICAL CHEMISTRY HOPPE-SEYLER | 1991年 / 372卷 / 03期
关键词
KUPFFER CELLS; LIPOPOLYSACCHARIDE; NEWCASTLE DISEASE VIRUS; PROSTAGLANDIN-E2; TNF PRECURSOR; TOLERANCE;
D O I
10.1515/bchm3.1991.372.1.157
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
Rat liver macrophages (Kupffer cells) secrete tumor necrosis factor-alpha (cachectin) after exposure to Newcastle disease virus or bacterial endotoxin. Macrophages treated with endotoxin become refractory and fail to release tumor necrosis factor-alpha to a secondary challenge with endotoxin. The acquisition of the refractory state is dose-dependent, requires the continuous presence of endotoxin for a minimum of 8 h, is transient, and reversible. Endotoxin, however, renders Kupffer cells unresponsive only to itself. When endotoxin-refractory macrophages are activated by Newcastle disease virus, they still secrete tumor necrosis factor-alpha in amounts expected with this stimulus. Immunoprecipitation studies show that the precursor of tumor necrosis factor-alpha is found only in lysates of endotoxin-sensitive, but not in refractory macrophages, thus arguing against a post-translational regulatory process. Whereas prostaglandin E2 inhibits the production of tumor necrosis factor-alpha in response to endotoxin and viruses, it does not appear to mediate the refractory state.
引用
收藏
页码:157 / 162
页数:6
相关论文
共 25 条
[1]   EFFECT OF GAMMA-INTERFERON ON CACHECTIN EXPRESSION BY MONONUCLEAR PHAGOCYTES - REVERSAL OF THE LPSD (ENDOTOXIN RESISTANCE) PHENOTYPE [J].
BEUTLER, B ;
TKACENKO, V ;
MILSARK, I ;
KROCHIN, N ;
CERAMI, A .
JOURNAL OF EXPERIMENTAL MEDICINE, 1986, 164 (05) :1791-1796
[2]   THE BIOLOGY OF CACHECTIN/TNF - A PRIMARY MEDIATOR OF THE HOST RESPONSE [J].
BEUTLER, B ;
CERAMI, A .
ANNUAL REVIEW OF IMMUNOLOGY, 1989, 7 :625-655
[3]  
BIRMELIN M, 1986, CELLS HEPATIC SINUSO, V1, P295
[4]   FILM DETECTION METHOD FOR TRITIUM-LABELED PROTEINS AND NUCLEIC-ACIDS IN POLYACRYLAMIDE GELS [J].
BONNER, WM ;
LASKEY, RA .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1974, 46 (01) :83-88
[5]   VIRUS-INDUCED VS ENDOTOXIN-INDUCED ACTIVATION OF LIVER MACROPHAGES [J].
BUSAM, KJ ;
HOMFELD, A ;
ZAWATZKY, R ;
KASTNER, S ;
BAUER, J ;
GEROK, W ;
DECKER, K .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1990, 191 (03) :577-582
[6]   BIOLOGY OF INTERLEUKIN-1 [J].
DINARELLO, CA .
FASEB JOURNAL, 1988, 2 (02) :108-115
[7]   RAT HEPATIC SINUSOIDAL ENDOTHELIAL-CELLS IN MONOLAYER-CULTURE - BIOCHEMICAL AND ULTRASTRUCTURAL CHARACTERISTICS [J].
EYHORN, S ;
SCHLAYER, HJ ;
HENNINGER, HP ;
DIETER, P ;
HERMANN, R ;
WOORTMENKER, M ;
BECKER, H ;
SCHAEFER, HE ;
DECKER, K .
JOURNAL OF HEPATOLOGY, 1988, 6 (01) :23-35
[8]   COMPARISON OF INVITRO-CELL CYTO-TOXIC ASSAYS FOR TUMOR NECROSIS FACTOR [J].
FLICK, DA ;
GIFFORD, GE .
JOURNAL OF IMMUNOLOGICAL METHODS, 1984, 68 (1-2) :167-175
[9]  
GAHRING LC, 1986, J IMMUNOL, V136, P2868
[10]   REPRESSION OF ALPHA-2-MACROGLOBULIN AND STIMULATION OF ALPHA-1-PROTEINASE INHIBITOR SYNTHESIS IN HUMAN MONONUCLEAR PHAGOCYTES BY ENDOTOXIN [J].
GANTER, U ;
BAUER, J ;
SCHULZHUOTARI, C ;
GEBICKEHAERTER, PJ ;
BEESER, H ;
GEROK, W .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1987, 169 (01) :13-20