Department of Mechanical and Aerospace Engineering, Princeton University, Princeton, NJ, USA.
Integr Biol (Camb). 2011 Oct;3(10):972-81. doi: 10.1039/c1ib00044f. Epub 2011 Sep 21.
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.
自 20 世纪 60 年代中期以来,人们已经广泛研究了红细胞(RBC)在静态和动态(即流动)条件下变形的机制。然而,十五年前才提出了变形诱导的生化反应和可能的信号转导。因此,红细胞变形和细胞信号转导动力学(即力传导)之间的基本关系仍不完全清楚。定量理解 RBC 中的力传导途径需要整合 RBC 变形的物理模型和细胞生化反应的研究。本文综述了红细胞变形的物理模型,从连续膜力学到静态和流动条件下的细胞骨架动力学,并详细阐述了变形诱导的 ATP 释放所涉及的机制联系。