INVOLVEMENT OF RAS-RELATED RHO-PROTEINS IN THE MECHANISMS OF ACTION OF CLOSTRIDIUM-DIFFICILE TOXIN-A AND TOXIN-B

被引:70
|
作者
DILLON, ST
RUBIN, EJ
YAKUBOVICH, M
POTHOULAKIS, C
LAMONT, JT
FEIG, LA
GILBERT, RJ
机构
[1] TUFTS UNIV,SCH MED,DEPT BIOCHEM,BOSTON,MA 02111
[2] TUFTS UNIV,SCH MED,DEPT MOLEC BIOL & MICROBIOL,BOSTON,MA 02111
[3] ST ELIZABETHS HOSP BOSTON,DEPT BIOMED RES,BOSTON,MA 02135
[4] BOSTON UNIV,SCH MED,DEPT GASTROENTEROL,BOSTON,MA 02118
关键词
D O I
10.1128/IAI.63.4.1421-1426.1995
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Toxins A and B of Clostridium difficile are responsible for pseudomembranous colitis, a disease that afflicts a substantial number of hospitalized patients treated with antibiotics, A major effect of these proteins is the disruption of the actin cytoskeleton. Recently, I. Just, G. Fritz, K. Aktories, M. Giry, M. R. Popoff, P. Boquet, S. Hegenbarth, and C. von Eichel-Streiber (J. Biol. Chem. 269:10706-10712, 1994) implicated Rho proteins as cellular targets of C. difficile toxin B, since pretreatment of cells or purified Rho with toxin prevented subsequent ADP-ribosylation of Rho by exoenzyme C3. Moreover, they showed that overexpression of Rho proteins in cells suppressed cell rounding normally associated with exposure of cells to C. difficile toxin B, Here we expand these findings by showing directly that Rho proteins are covalently modified by both C. difficile toxins A and B. In addition, we demonstrate that the stability of toxin-modified Rho in NIH 3T3 cells is dramatically reduced. Finally, we show that C. difficile toxins A and Il do not have similar effects on the closely related Rac and CDC42 GTP-binding proteins.
引用
收藏
页码:1421 / 1426
页数:6
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