PATHOGENESIS OF SHIGELLA DIARRHEA .17. A MAMMALIAN-CELL MEMBRANE GLYCOLIPID, GB3, IS REQUIRED BUT NOT SUFFICIENT TO CONFER SENSITIVITY TO SHIGA TOXIN

被引:47
作者
JACEWICZ, MS
MOBASSALEH, M
GROSS, SK
BALASUBRAMANIAN, KA
DANIEL, PF
RAGHAVAN, S
MCCLUER, RH
KEUSCH, GT
机构
[1] TUFTS UNIV NEW ENGLAND MED CTR,DIV GEOGR MED & INFECT DIS,BOSTON,MA 02111
[2] TUFTS UNIV NEW ENGLAND MED CTR,DIV PEDIAT GASTROENTEROL,BOSTON,MA 02111
[3] EUNICE KENNEDY SHRIVER CTR MENTAL RETARDAT INC,DEPT BIOCHEM,WALTHAM,MA 02254
[4] CHRISTIAN MED COLL & HOSP,VELLORE 632002,INDIA
关键词
D O I
10.1093/infdis/169.3.538
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Shiga toxin recognizes a galactose-alpha 1 --> 4-galactose terminal glycolipid, globotriaosylceramide (Gb3), in sensitive mammalian cells and is translocated by endocytosis to the cytoplasm, where it blocks protein synthesis. To determine if Gb3 is both required and sufficient for toxicity, Gb3 content in cells was altered by blocking key biosynthetic or degradative path enzymes with specific inhibitors. The resulting decrease or increase in cellular Gb3 was associated with a decrease or increase in binding of and response to Shiga toxin. Toxin-resistant Gb3-deficient variants of sensitive cells fused with liposomes containing Gb3 but not globotetraosylceramide (Gb4) became susceptible, whereas fusion of Gb3 liposomes to naturally resistant Gb3-deficient CHO cells increased toxin binding but not cytotoxicity. These data demonstrate that Gb3 is required, but not sufficient, for the action of Shiga toxin and suggest the existence of a toxin translocation mechanism linked to surface glycolipids that is not expressed in CHO cells.
引用
收藏
页码:538 / 546
页数:9
相关论文
共 33 条
[1]  
Acheson DWK, 1991, SOURCEBOOK BACTERIAL, P415
[2]   SYNTHESIS OF (+)-1,5-DIDEOXY-1,5-IMINO-D-GALACTITOL, A POTENT ALPHA-D-GALACTOSIDASE INHIBITOR [J].
BERNOTAS, RC ;
PEZZONE, MA ;
GANEM, B .
CARBOHYDRATE RESEARCH, 1987, 167 :305-311
[3]   ALTERATION OF THE GLYCOLIPID BINDING-SPECIFICITY OF THE PIG EDEMA TOXIN FROM GLOBOTETRAOSYL TO GLOBOTRIASOYL CERAMIDE ALTERS INVIVO TISSUE TARGETING AND RESULTS IN A VEROTOXIN-1 LIKE DISEASE IN PIGS [J].
BOYD, B ;
TYRRELL, G ;
MALONEY, M ;
GYLES, C ;
BRUNTON, J ;
LINGWOOD, C .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 177 (06) :1745-1753
[4]  
BROWN JE, 1983, 7TH P INT S GLYC LUN, P678
[5]   MECHANISM OF FLUORESCENCE CONCENTRATION QUENCHING OF CARBOXYFLUORESCEIN IN LIPOSOMES - ENERGY-TRANSFER TO NONFLUORESCENT DIMERS [J].
CHEN, RF ;
KNUTSON, JR .
ANALYTICAL BIOCHEMISTRY, 1988, 172 (01) :61-77
[6]   DIFFERENTIAL ENTRY OF RICIN INTO MALIGNANT AND NORMAL RAT HEPATOCYTES [J].
DECASTEL, M ;
HAENTJENS, G ;
AUBERY, M ;
GOUSSAULT, Y .
EXPERIMENTAL CELL RESEARCH, 1989, 180 (02) :399-408
[7]   ISOLATION AND CHARACTERIZATION OF FUNCTIONAL SHIGA TOXIN SUBUNITS AND RENATURED HOLOTOXIN [J].
DONOHUEROLFE, A ;
JACEWICZ, M ;
KEUSCH, GT .
MOLECULAR MICROBIOLOGY, 1989, 3 (09) :1231-1236
[8]   PURIFICATION OF SHIGA TOXIN AND SHIGA-LIKE TOXIN-I AND TOXIN-II BY RECEPTOR ANALOG AFFINITY-CHROMATOGRAPHY WITH IMMOBILIZED P1 GLYCOPROTEIN AND PRODUCTION OF CROSS-REACTIVE MONOCLONAL-ANTIBODIES [J].
DONOHUEROLFE, A ;
ACHESON, DWK ;
KANE, AV ;
KEUSCH, GT .
INFECTION AND IMMUNITY, 1989, 57 (12) :3888-3893
[9]   PATHOGENESIS OF SHIGELLA DIARRHEA .9. SIMPLIFIED HIGH-YIELD PURIFICATION OF SHIGELLA TOXIN AND CHARACTERIZATION OF SUBUNIT COMPOSITION AND FUNCTION BY THE USE OF SUBUNIT-SPECIFIC MONOCLONAL AND POLYCLONAL ANTIBODIES [J].
DONOHUEROLFE, A ;
KEUSCH, GT ;
EDSON, C ;
THORLEYLAWSON, D ;
JACEWICZ, M .
JOURNAL OF EXPERIMENTAL MEDICINE, 1984, 160 (06) :1767-1781
[10]   SITE OF ACTION OF A VERO TOXIN (VT2) FROM ESCHERICHIA-COLI O157-H7 AND OF SHIGA TOXIN ON EUKARYOTIC RIBOSOMES - RNA N-GLYCOSIDASE ACTIVITY OF THE TOXINS [J].
ENDO, Y ;
TSURUGI, K ;
YUTSUDO, T ;
TAKEDA, Y ;
OGASAWARA, T ;
IGARASHI, K .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1988, 171 (1-2) :45-50