Mitochondrial and bioenergetic dysfunction in human hepatic cells infected with dengue 2 virus

被引:95
作者
El-Bacha, Tatiana [1 ]
Midlej, Victor
Pereira da Silva, Ana Paula [1 ,2 ]
da Costa, Leandro Silva [1 ]
Benchimol, Marlene
Galina, Antonio [2 ]
Da Poian, Andrea T. [1 ]
机构
[1] Univ Fed Rio de Janeiro, Inst Bioquim Med, Lab Bioquim Virus, BR-21941590 Rio De Janeiro, Brazil
[2] Univ Fed Rio de Janeiro, Inst Bioquim Med, Lab Bioenerget & Fisiol Mitocondrial, BR-21941590 Rio De Janeiro, Brazil
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE | 2007年 / 1772卷 / 10期
关键词
dengue virus infection; mitochondrial dysfunction; metabolism; energy charge; apoptosis; HepG2; cell;
D O I
10.1016/j.bbadis.2007.08.003
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
Dengue virus infection affects millions of people all over the world. Although the clinical manifestations of dengue virus-induced diseases are known, the physiopathological mechanisms involved in deteriorating cellular function are not yet understood. In this study we evaluated for the first time the associations between dengue virus-induced cell death and mitochondrial function in HepG2, a human hepatoma cell line. Dengue virus infection promoted changes in mitochondrial bioenergetics, such as an increase in cellular respiration and a decrease in A Delta psi(m). These alterations culminated in a 20% decrease in ATP content and a 15% decrease in the energy charge of virus-infected cells. Additionally, virus-infected cells showed several ultrastructural alterations, including mitochondria swelling and other morphological changes typical of the apoptotic process. The alterations in mitochondrial physiology and energy homeostasis preceded cell death. These results indicate that HepG2 cells infected with dengue virus are under metabolic stress and that mitochondrial dysfunction and alterations in cellular ATP balance may be related to the pathogenesis of dengue virus infection. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:1158 / 1166
页数:9
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