Induction of autophagy by anthrax lethal toxin

被引:20
作者
Tan, Yian Kim [1 ]
Kusuma, Caroline M. [2 ]
St John, Lena J. [2 ]
Vu, Hao A. [2 ]
Alibek, Kenneth [2 ]
Wu, Aiguo [2 ]
机构
[1] George Mason Univ, Mol & Microbiol Dept, Coll Sci, Manassas, VA 22010 USA
[2] AFG Biosolut Inc, Gaithersburg, MD 20877 USA
关键词
Autophagy; Bacillus anthracis; Anthrax; Lethal factor; Protective antigen; LC3; Autophagosome; MACROPHAGE CELL-DEATH; MONITORING AUTOPHAGY; PROTECTIVE ANTIGEN; YEAST; 3-METHYLADENINE; PROTEINS; RECEPTOR;
D O I
10.1016/j.bbrc.2008.12.048
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
Autophagy is an evolutionary conserved intracellular process whereby cells break down long-lived proteins and organelles. Accumulating evidences suggest increasing physiological significance of autophagy in pathogenesis of infectious diseases. Anthrax lethal toxin (LT) exerts its influence oil numerous cells and herein, we report a novel effect of LT-induced autophagy on mammalian cells. Several autophagy biochemical markers including LC3-II conversion, increased punctuate distribution of GFP-LC3 and development of acidic vesicular organelles (AVO) were detected in cells treated with LT. Analysis of individual LT component revealed a moderate increase in LC3-II conversion for protective antigen-treated cells, whereas the LC3-II level in lethal factor-treated cells remained unchanged. In addition, our preliminary findings suggest a protective role Of autophagy in LT intoxication as autophagy inhibition resulted in accelerated cell death. This study presents a hitherto undescribed effect of LT-induced autophagy on cells and provides the groundwork for future studies oil the implication of autophagy in anthrax pathogenesis. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:293 / 297
页数:5
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