Insights into the redox biology of Trypanosoma cruzi:: Trypanothione metabolism and oxidant detoxification

被引:122
作者
Irigoin, Florencia [1 ,3 ]
Cibils, Lucia [2 ,3 ]
Comini, Marcelo A. [4 ]
Wilkinson, Shane R. [5 ]
Flohe, Leopold [6 ]
Radi, Rafael [2 ,3 ]
机构
[1] Univ Republica, Fac Med, Dept Histol & Embriol, Montevideo, Uruguay
[2] Univ Republica, Fac Med, Dept Bioquim, Montevideo, Uruguay
[3] Univ Republica, Fac Med, Ctr Free Rad & Biomed Res, Montevideo, Uruguay
[4] Heidelberg Univ, Biochem Zentrum, D-69120 Heidelberg, Germany
[5] Queen Mary Univ London, Sch Biol & Chem Sci, London, England
[6] MOLISA GmbH, D-39118 Magdeburg, Germany
关键词
kinetoplastida; trypasonoma; trypanothione; glutathione; polyamines; Chagas' disease; reactive oxygen species; antioxidant defenses;
D O I
10.1016/j.freeradbiomed.2008.05.028
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
Trypanosoma cruzi is the etiologic agent of Chagas' disease, an infection that affects several million people in Latin America. With no immediate prospect of a vaccine and problems associated with current chemotherapies, the development of new treatments is all urgent priority. Several aspects of the redox metabolism of this parasite differ enough from those in the mammalian host to be considered targets for drug development. Here, we review the information about a trypanosomatid-specific molecule centrally involved in redox metabolism, the dithiol trypanothione, and the main effectors of cellular antioxidant defense. We focus mainly on data from T cruzi, making comparisons with other trypanosomatids whenever possible. in these Parasites trypanothione participates in Crucial thiol-disulfide exchange reactions and serves as electron donor in different metabolic pathways, from synthesis of DNA precursors to oxidant detoxification. Interestingly, the levels of several enzymes involved in trypanothione metabolism and oxidant detoxification increase during the transformation of T cruzi to its mammalian-infective form and the overexpression of some of them has been associated with increased resistance to macrophage-dependent oxidative killing. Together, the evidence suggests a central role of the trypanothione-dependent antioxidant systems in the infection process. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:733 / 742
页数:10
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