| Literature DB >> 24867952 |
Douglas A Pace1, Ciara A McKnight2, Jing Liu3, Veronica Jimenez1, Silvia N J Moreno4.
Abstract
During invasion and egress from their host cells, Apicomplexan parasites face sharp changes in the surrounding calcium ion (Ca(2+)) concentration. Our work with Toxoplasma gondii provides evidence for Ca(2+) influx from the extracellular milieu leading to cytosolic Ca(2+) increase and enhancement of virulence traits, such as gliding motility, conoid extrusion, microneme secretion, and host cell invasion. Assays of Mn(2+) and Ba(2+) uptake do not support a canonical store-regulated Ca(2+) entry mechanism. Ca(2+) entry was blocked by the L-type Ca(2+) channel inhibitor nifedipine and stimulated by the increase in cytosolic Ca(2+) and by the specific L-type Ca(2+) channel agonist Bay K-8644. Our results demonstrate that Ca(2+) entry is critical for parasite virulence. We propose a regulated Ca(2+) entry mechanism activated by cytosolic Ca(2+) that has an enhancing effect on invasion-linked traits.Entities:
Keywords: Calcium; Cell Invasion; Conoid Extrusion; Fluorescence; Gliding Motility; Nifedipine; Parasite; Protozoan; Signaling; Toxoplasma gondii
Mesh:
Substances:
Year: 2014 PMID: 24867952 PMCID: PMC4094074 DOI: 10.1074/jbc.M114.565390
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157