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Phosphoinositide Metabolism Links cGMP-Dependent Protein Kinase G to Essential Ca(2+) Signals at Key Decision Points in the Life Cycle of Malaria Parasites

Many critical events in the Plasmodium life cycle rely on the controlled release of Ca(2+) from intracellular stores to activate stage-specific Ca(2+)-dependent protein kinases. Using the motility of Plasmodium berghei ookinetes as a signalling paradigm, we show that the cyclic guanosine monophospha...

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Detalles Bibliográficos
Autores principales: Brochet, Mathieu, Collins, Mark O., Smith, Terry K., Thompson, Eloise, Sebastian, Sarah, Volkmann, Katrin, Schwach, Frank, Chappell, Lia, Gomes, Ana Rita, Berriman, Matthew, Rayner, Julian C., Baker, David A., Choudhary, Jyoti, Billker, Oliver
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3942320/
https://www.ncbi.nlm.nih.gov/pubmed/24594931
http://dx.doi.org/10.1371/journal.pbio.1001806
Descripción
Sumario:Many critical events in the Plasmodium life cycle rely on the controlled release of Ca(2+) from intracellular stores to activate stage-specific Ca(2+)-dependent protein kinases. Using the motility of Plasmodium berghei ookinetes as a signalling paradigm, we show that the cyclic guanosine monophosphate (cGMP)-dependent protein kinase, PKG, maintains the elevated level of cytosolic Ca(2+) required for gliding motility. We find that the same PKG-dependent pathway operates upstream of the Ca(2+) signals that mediate activation of P. berghei gametocytes in the mosquito and egress of Plasmodium falciparum merozoites from infected human erythrocytes. Perturbations of PKG signalling in gliding ookinetes have a marked impact on the phosphoproteome, with a significant enrichment of in vivo regulated sites in multiple pathways including vesicular trafficking and phosphoinositide metabolism. A global analysis of cellular phospholipids demonstrates that in gliding ookinetes PKG controls phosphoinositide biosynthesis, possibly through the subcellular localisation or activity of lipid kinases. Similarly, phosphoinositide metabolism links PKG to egress of P. falciparum merozoites, where inhibition of PKG blocks hydrolysis of phosphatidylinostitol (4,5)-bisphosphate. In the face of an increasing complexity of signalling through multiple Ca(2+) effectors, PKG emerges as a unifying factor to control multiple cellular Ca(2+) signals essential for malaria parasite development and transmission.