Chaperone expression profiles correlate with distinct physiological states of Plasmodium falciparum in malaria patients
| Autor: | Johanna P. Daily, Utpal Tatu, Rani Pallavi, Pragyan Acharya, Syama Chandran |
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| Rok vydání: | 2010 |
| Předmět: |
lcsh:Arctic medicine. Tropical medicine
lcsh:RC955-962 Plasmodium falciparum Biochemistry Models Biological lcsh:Infectious and parasitic diseases medicine Cluster Analysis Humans lcsh:RC109-216 HSP90 Heat-Shock Proteins Malaria Falciparum Cellular compartment biology Gene Expression Profiling Research Computational Biology biology.organism_classification medicine.disease Hsp90 Cell biology Up-Regulation Gene expression profiling Infectious Diseases Cytoplasm Chaperone (protein) biology.protein Parasitology Neural Networks Computer Starvation response Glycolysis Malaria Molecular Chaperones |
| Zdroj: | Malaria Journal Malaria Journal, Vol 9, Iss 1, p 236 (2010) |
| ISSN: | 1475-2875 |
| Popis: | Background Molecular chaperones have been shown to be important in the growth of the malaria parasite Plasmodium falciparum and inhibition of chaperone function by pharmacological agents has been shown to abrogate parasite growth. A recent study has demonstrated that clinical isolates of the parasite have distinct physiological states, one of which resembles environmental stress response showing up-regulation of specific molecular chaperones. Methods Chaperone networks operational in the distinct physiological clusters in clinical malaria parasites were constructed using cytoscape by utilizing their clinical expression profiles. Results Molecular chaperones show distinct profiles in the previously defined physiologically distinct states. Further, expression profiles of the chaperones from different cellular compartments correlate with specific patient clusters. While cluster 1 parasites, representing a starvation response, show up-regulation of organellar chaperones, cluster 2 parasites, which resemble active growth based on glycolysis, show up-regulation of cytoplasmic chaperones. Interestingly, cytoplasmic Hsp90 and its co-chaperones, previously implicated as drug targets in malaria, cluster in the same group. Detailed analysis of chaperone expression in the patient cluster 2 reveals up-regulation of the entire Hsp90-dependent pro-survival circuitries. In addition, cluster 2 also shows up-regulation of Plasmodium export element (PEXEL)-containing Hsp40s thought to have regulatory and host remodeling roles in the infected erythrocyte. Conclusion In all, this study demonstrates an intimate involvement of parasite-encoded chaperones, PfHsp90 in particular, in defining pathogenesis of malaria. |
| Databáze: | OpenAIRE |
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