Journalartikel

Jahr der Veröffentlichung: 2010

Seiten: 37388-37395

Zeitschrift: Journal of Biological Chemistry

Bandnummer: 285

Heftnummer: 48

ISSN: 0021-9258

eISSN: 1083-351X

Open Access Status: Hybrid

DOI Link: https://doi.org/10.1074/jbc.M110.123323

Verlag: Elsevier

Abstract: 
Malaria-associated pathology is caused by the continuous expansion of Plasmodium parasites inside host erythrocytes. To maintain a reducing intracellular milieu in an oxygen-rich environment, malaria parasites have evolved a complex antioxidative network based on two central electron donors, glutathione and thioredoxin. Here, we dissected the in vivo roles of both redox pathways by gene targeting of the respective NADPH-dependent disulfide reductases. We show that Plasmodium berghei glutathione reductase and thioredoxin reductase are dispensable for proliferation of the pathogenic blood stages. Intriguingly, glutathione reductase is vital for extracellular parasite development inside the insect vector, whereas thioredoxin reductase is dispensable during the entire parasite life cycle. Our findings suggest that glutathione reductase is the central player of the parasite redox network, whereas thioredoxin reductase fulfils a specialized and dispensable role for P. berghei. These results also indicate redundant roles of the Plasmodium redox pathways during the pathogenic blood phase and query their suitability as promising drug targets for antimalarial intervention strategies.

Harvard-Zitierstil: Buchholz, K., Putrianti, E., Rahlfs, S., Schirmer, R., Becker, K. and Matuschewski, K. (2010) Molecular Genetics Evidence for the in Vivo Roles of the Two Major NADPH-dependent Disulfide Reductases in the Malaria Parasite, Journal of Biological Chemistry, 285(48), pp. 37388-37395. https://doi.org/10.1074/jbc.M110.123323

APA-Zitierstil: Buchholz, K., Putrianti, E., Rahlfs, S., Schirmer, R., Becker, K., & Matuschewski, K. (2010). Molecular Genetics Evidence for the in Vivo Roles of the Two Major NADPH-dependent Disulfide Reductases in the Malaria Parasite. Journal of Biological Chemistry. 285(48), 37388-37395. https://doi.org/10.1074/jbc.M110.123323