Lavazec Catherine, Deplaine Guillaume, Safeukui Innocent, Perrot Sylvie, Milon Geneviève, Mercereau-Puijalon Odile, David Peter H, Buffet Pierre
Unité d'Immunologie Moléculaire des Parasites, Institut Pasteur, Paris, France.
Methods Mol Biol. 2013;923:291-7. doi: 10.1007/978-1-62703-026-7_20.
The altered deformability of erythrocytes infected with Plasmodium falciparum is central in malaria -pathogenesis, as it influences the hemodynamic properties of the infected cell and its retention in the spleen. Exported parasite proteins, as well as the shape and volume of the parasite itself, influence the deformability of the infected erythrocyte. To explore changes in erythrocyte deformability, we have developed a new method, called microsphiltration, based on filtration of erythrocytes through a mixture of metal microspheres that mimic the geometry of inter-endothelial splenic slits. As P. falciparum develops in its host cell, the retention rates observed in microspheres correlate with the progressive decrease of erythrocyte deformability and with the retention rates in the spleen. The yields of microsphiltration separation allow for molecular analyses of subpopulations with distinct mechanical phenotypes.
感染恶性疟原虫的红细胞变形性改变在疟疾发病机制中至关重要,因为它会影响受感染细胞的血液动力学特性及其在脾脏中的滞留情况。输出的寄生虫蛋白以及寄生虫本身的形状和体积,都会影响受感染红细胞的变形性。为了探究红细胞变形性的变化,我们开发了一种新方法,称为微球过滤法,该方法基于红细胞通过模拟脾内皮细胞间裂隙几何形状的金属微球混合物进行过滤。随着恶性疟原虫在其宿主细胞中发育,在微球中观察到的滞留率与红细胞变形性的逐渐降低以及在脾脏中的滞留率相关。微球过滤分离的产量允许对具有不同机械表型的亚群进行分子分析。