Red blood cell dynamics: from cell deformation to ATP release

被引:63
|
作者
Wan, Jiandi [1 ]
Forsyth, Alison M. [1 ]
Stone, Howard A. [1 ]
机构
[1] Princeton Univ, Dept Mech & Aerosp Engn, Princeton, NJ 08544 USA
关键词
SIGNAL-TRANSDUCTION PATHWAY; ERYTHROCYTE-MEMBRANE; MOLECULAR ADHESION; EXTRACELLULAR ATP; PANNEXIN; REGULATOR; FLOW; CHANNELS; MODEL; MOTION;
D O I
10.1039/c1ib00044f
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The mechanisms of red blood cell (RBC) deformation under both static and dynamic, i.e., flow, conditions have been studied extensively since the mid 1960s. Deformation-induced biochemical reactions and possible signaling in RBCs, however, were proposed only fifteen years ago. Therefore, the fundamental relationship between RBC deformation and cellular signaling dynamics i.e., mechanotransduction, remains incompletely understood. Quantitative understanding of the mechanotransductive pathways in RBCs requires integrative studies of physical models of RBC deformation and cellular biochemical reactions. In this article we review the physical models of RBC deformation, spanning from continuum membrane mechanics to cellular skeleton dynamics under both static and flow conditions, and elaborate the mechanistic links involved in deformation-induced ATP release.
引用
收藏
页码:972 / 981
页数:10
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