TY - JOUR
T1 - A numerical model of a red blood cell infected by Plasmodium falciparum malaria
T2 - coupling cell mechanics with ligand-receptor interactions
AU - Ishida, Shunichi
AU - Imai, Yohsuke
AU - Ichikawa, Yuki
AU - Nix, Stephanie
AU - Matsunaga, Daiki
AU - Omori, Toshihiro
AU - Ishikawa, Takuji
N1 - Funding Information:
This research was supported by JSPS KAKENHI [grant numbers 25000008, 26107703].
Publisher Copyright:
© 2016 Informa UK Limited, trading as Taylor & Francis Group.
PY - 2016/1/1
Y1 - 2016/1/1
N2 - We developed a numerical model of the behavior of a red blood cell infected by Plasmodium falciparum malaria on a wall in shear flow. The fluid and solid mechanics of an infected red blood cell (Pf-IRBC) were coupled with the biochemical interaction of ligand-receptor bindings. We used the boundary element method for fluid mechanics, the finite element method for membrane mechanics, and the Monte Carlo method for ligand-receptor interactions. We simulated the behavior of a Pf-IRBC in shear flow, focusing on the effects of bond type. For slip bonds, the Pf-IRBC exhibited firm adhesion, tumbling motion, and tank-treading motion, depending on the applied shear rate. The behavior of catch bonds resembled that of slip bonds, except for a ‘catch’ state at high shear stress. When the reactive compliance decreased to a value in the order of 10-2 nm, both the slip and catch bonds behaved like an ideal bond. Such bonds do not respond to the force applied to the bond, and the velocity is stabilized at a high shear rate. Finally, we compared the numerical results with previous experiments for A4- and ItG-infected cells. We found that the interaction between PfEMP1 and ICAM-1 could be a nearly ideal bond, with a dissociation rate ranging from 30 s-1 to 100 s-1.
AB - We developed a numerical model of the behavior of a red blood cell infected by Plasmodium falciparum malaria on a wall in shear flow. The fluid and solid mechanics of an infected red blood cell (Pf-IRBC) were coupled with the biochemical interaction of ligand-receptor bindings. We used the boundary element method for fluid mechanics, the finite element method for membrane mechanics, and the Monte Carlo method for ligand-receptor interactions. We simulated the behavior of a Pf-IRBC in shear flow, focusing on the effects of bond type. For slip bonds, the Pf-IRBC exhibited firm adhesion, tumbling motion, and tank-treading motion, depending on the applied shear rate. The behavior of catch bonds resembled that of slip bonds, except for a ‘catch’ state at high shear stress. When the reactive compliance decreased to a value in the order of 10-2 nm, both the slip and catch bonds behaved like an ideal bond. Such bonds do not respond to the force applied to the bond, and the velocity is stabilized at a high shear rate. Finally, we compared the numerical results with previous experiments for A4- and ItG-infected cells. We found that the interaction between PfEMP1 and ICAM-1 could be a nearly ideal bond, with a dissociation rate ranging from 30 s-1 to 100 s-1.
KW - Nanomedicine molecular science
KW - cell adhesion
KW - computational biomechanics
KW - malaria
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U2 - 10.1080/14686996.2016.1211462
DO - 10.1080/14686996.2016.1211462
M3 - Article
AN - SCOPUS:85019102068
SN - 1468-6996
VL - 17
SP - 454
EP - 461
JO - Science and Technology of Advanced Materials
JF - Science and Technology of Advanced Materials
IS - 1
ER -