THE PLASMA-MEMBRANE INTERNALIZATION AND RECYCLING IS ENHANCED IN MACROPHAGES UPON ACTIVATION WITH GAMMA-INTERFERON AND LIPOPOLYSACCHARIDE - A STUDY USING THE FLUORESCENT-PROBE TRIMETHYLAMINODIPHENYLHEXATRIENE

被引:12
作者
ILLINGER, D
POINDRON, P
GLASSER, N
MODOLLEL, M
KUHRY, JG
机构
[1] UNIV LOUIS PASTEUR, FAC PHARM,DEPT IMMUNOL,BIOPHYS LAB,74 ROUTE RHIN, BP 24, F-67401 ILLKIRCH GRAFFENSTADEN, FRANCE
[2] CNRS, BIOPHYS LAB, UA 491, ILLKIRCH GRAFFENSTADEN, FRANCE
[3] MAX PLANCK INST IMMUNBIOL, W-7800 FREIBURG, GERMANY
关键词
Endocytosis; Fluorescent probe; Macrophage activation; Pinocytosis; Plasma membrane; Trimethylamino-diphenylhexatriene;
D O I
10.1016/0005-2736(90)90241-F
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
The lipophilic fluorescent probe trimethylaminodiphenylhexatriene (TMA-DPH), previously used as a plasma membrane marker in membrane fluidity and exocytosis studies, was shown, to monitor the plasma-membrane internalization-recycling shuttle movement in cells. Using this approach we present here kinetic and dose-response data, which give evidence that the plasma membrane flow is enhanced in bone marrow macrophages from various mouse strains, upon in vitro activation with gamma interferon (IFN-γ) or bacterial lipopolysaccharide (LPS), within physiological dose ranges. The effect studied evolved in line with the usual development kinetics of macrophage activation. Complementary assays on membrane fluidity, surface charge density and membrane surface indicated no related changes. From these experiments it is concluded that the observed enhancement of the plasma membrane traffic does not originate from specific limited membrane modifications, but is merely a particular feature of the overall macrophage activation. © 1990.
引用
收藏
页码:82 / 87
页数:6
相关论文
共 24 条
[1]   MOLECULAR-INTERACTIONS IN MACROPHAGE ACTIVATION [J].
ADAMS, DO .
IMMUNOLOGY TODAY, 1989, 10 (02) :33-35
[2]   MOLECULAR TRANSDUCTIONAL MECHANISMS BY WHICH IFN-GAMMA AND OTHER SIGNALS REGULATE MACROPHAGE DEVELOPMENT [J].
ADAMS, DO ;
HAMILTON, TA .
IMMUNOLOGICAL REVIEWS, 1987, 97 :5-27
[3]   THE CELL BIOLOGY OF MACROPHAGE ACTIVATION [J].
ADAMS, DO ;
HAMILTON, TA .
ANNUAL REVIEW OF IMMUNOLOGY, 1984, 2 :283-318
[4]  
ADAMS DO, 1988, INFLAMMATION BASIC P, P471
[5]   PLASMA-MEMBRANE FLUIDITY IN ISOLATED RAT HEPATOCYTES - A COMPARATIVE-STUDY USING DPH AND TMA-DPH AS FLUORESCENT-PROBES [J].
BENEDETTI, A ;
FERRETTI, G ;
CURATOLA, G ;
BRUNELLI, E ;
JEZEQUEL, AM ;
ORLANDI, F .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 1989, 4 (03) :221-227
[6]   EXOCYTOSIS OF PINOCYTOSED FLUID IN CULTURED-CELLS - KINETIC EVIDENCE FOR RAPID TURNOVER AND COMPARTMENTATION [J].
BESTERMAN, JM ;
AIRHART, JA ;
WOODWORTH, RC ;
LOW, RB .
JOURNAL OF CELL BIOLOGY, 1981, 91 (03) :716-727
[7]   RESTING PLASMA-MEMBRANE POTENTIAL OF RAT PERITONEAL MAST-CELLS IS SET PREDOMINANTLY BY THE SODIUM-PUMP [J].
BRONNER, C ;
MOUSLI, M ;
ELENO, N ;
LANDRY, Y .
FEBS LETTERS, 1989, 255 (02) :401-404
[8]   A FLUORESCENT HYDROPHOBIC PROBE USED FOR MONITORING THE KINETICS OF EXOCYTOSIS PHENOMENA [J].
BRONNER, C ;
LANDRY, Y ;
FONTENEAU, P ;
KUHRY, JG .
BIOCHEMISTRY, 1986, 25 (08) :2149-2154
[9]  
COHN ZA, 1978, J IMMUNOL, V121, P813
[10]  
DECHASTELLIER C, 1987, EUR J CELL BIOL, V44, P112