Division of Applied Mathematics, Brown University, Providence, Rhode Island, USA.
Biophys J. 2011 May 4;100(9):2084-93. doi: 10.1016/j.bpj.2011.03.027.
Red blood cells (RBCs) infected by the Plasmodium falciparum (Pf-RBCs) parasite lose their membrane deformability and they also exhibit enhanced cytoadherence to vascular endothelium and other healthy and infected RBCs. The combined effect may lead to severe disruptions of normal blood circulation due to capillary occlusions. Here we extend the adhesion model to investigate the adhesive dynamics of Pf-RBCs as a function of wall shear stress (WSS) and other parameters using a three-dimensional, multiscale RBC model. Several types of adhesive behavior are identified, including firm adhesion, flipping dynamics, and slow slipping along the wall. In particular, the flipping dynamics of Pf-RBCs observed in experiments appears to be due to the increased stiffness of infected cells and the presence of the solid parasite inside the RBC, which may cause an irregular adhesion behavior. Specifically, a transition from crawling dynamics to flipping behavior occurs at a Young's modulus approximately three times larger than that of healthy RBCs. The simulated dynamics of Pf-RBCs is in excellent quantitative agreement with available microfluidic experiments if the force exerted on the receptors and ligands by an existing bond is modeled as a nonlinear function of WSS.
受疟原虫(Pf)感染的红细胞(RBC)失去了膜的变形能力,并且它们还表现出增强的细胞黏附性,黏附于血管内皮细胞和其他健康及感染的 RBC。这种综合效应可能导致毛细血管阻塞而严重扰乱正常的血液循环。在这里,我们扩展了黏附模型,以使用三维、多尺度 RBC 模型来研究 Pf-RBC 在壁面剪切应力(WSS)和其他参数下的黏附动力学。确定了几种类型的黏附行为,包括牢固黏附、翻转动力学和沿壁缓慢滑动。特别是,实验中观察到的 Pf-RBC 的翻转动力学似乎是由于感染细胞的刚性增加以及 RBC 内存在固体寄生虫所致,这可能导致不规则的黏附行为。具体来说,在杨氏模量大约是健康 RBC 的三倍时,从爬行动力学到翻转行为的转变发生。如果将现有键上的力施加在受体和配体上的模型表示为 WSS 的非线性函数,则 Pf-RBC 的模拟动力学与现有的微流控实验非常吻合。