Coupled positive feedbacks provoke slow induction plus fast switching in apoptosis

被引:15
作者
Choi, Hyung-Seok
Han, Soohee
Yokota, Hiroki
Cho, Kwang-Hyun [1 ]
机构
[1] Seoul Natl Univ, BioMAX Inst, Seoul 151818, South Korea
[2] Seoul Natl Univ, Interdisciplinary Program Bioinformat, Seoul 151747, South Korea
[3] Indiana Univ Purdue Univ, Dept Biomed Engn, Indianapolis, IN 46202 USA
[4] Indiana Univ Purdue Univ, Dept Anat & Cell Biol, Indianapolis, IN 46202 USA
[5] Seoul Natl Univ, Coll Med, Seoul 110799, South Korea
来源
FEBS LETTERS | 2007年 / 581卷 / 14期
关键词
apoptosis; caspase-3; activation; long induction; fast switching; coupled positive feedbacks; simulation analysis;
D O I
10.1016/j.febslet.2007.05.016
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
Apoptosis is a form of a programmed cell death for multicellular organisms to remove unwanted or damaged cells. This critical choice of cellular fate is an all-or-none process, but its dynamics remains unraveled. The switch-like apoptotic decision has to be reliable, and once a pro-apoptotic fate is determined it requires fast and irreversible execution. One of the key regulators in apoptosis is caspase-3. Interestingly, activated caspase-3 quickly executes apoptosis, but it takes considerable time to activate it. Here, we have analyzed this "slow induction plus fast switching" mechanism of caspase-3 through mathematical modeling and computational simulation. First, we have shown that two positive feedbacks, composed of caspase-8 and XIAP, are essential for the "slow induction plus fast switching" behavior of caspase-3. Second, we have found that XIAP in the feedback loops primarily regulates induction time of caspase-3. In many cancer cells activation of caspase-3 is suppressed. Our results suggest that reinforcement of the positive feedback by XIAP, which relieves XIAP-mediated caspase-3 inhibition, might favor a pro-apoptotic cellular fate. (c) 2007 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:2684 / 2690
页数:7
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