Khairy Khaled, Foo Jijinn, Howard Jonathon
Max Planck Institute of Molecular Cell Biology and Genetics, Pfotenhauerstrasse 108, D-01307 Dresden, Germany.
Cell Mol Bioeng. 2010 Sep 1;1(2-3):173-181. doi: 10.1007/s12195-008-0019-5.
Cells and organelles are shaped by the chemical and physical forces that bend cell membranes. The human red blood cell (RBC) is a model system for studying how such forces determine cell morphology. It is thought that RBCs, which are typically biconcave discoids, take the shape that minimizes their membrane-bending energies, subject to the constraints of fixed area and volume. However, recently it has been hypothesized that shear elasticity arising from the membrane-associated cytoskeleton (MS) is necessary to account for shapes of real RBCs, especially ones with highly curved features such as echinocytes. In this work we tested this hypothesis by following RBC shape changes using spherical harmonic series expansions of theoretical cell surfaces and those estimated from 3D confocal microscopy images of live cells. We found (i) quantitative agreement between shapes obtained from the theoretical model including the MS and real cells, (ii) that weakening the MS, by using urea (which denatures spectrin), leads to the theoretically predicted gradual decrease in spicule number of echinocytes, (iii) that the theory predicts that the MS is essential for stabilizing the discocyte morphology against changes in lipid composition, and that without it, the shape would default to the elliptocyte (a biconcave ellipsoid), (iv) that we were able to induce RBCs to adopt the predicted elliptocyte morphology by treating healthy discocytes with urea. The latter observation is consistent with the known connection between the blood disease hereditary elliptocytosis and spectrin mutations that weaken the cell cortex. We conclude that while the discocyte, in absence of shear, is indeed a minimum energy shape, its stabilization in healthy RBCs requires the MS, and that elliptocytosis can be explained based on purely mechanical considerations.
细胞和细胞器的形状是由使细胞膜弯曲的化学和物理力所塑造的。人类红细胞(RBC)是研究此类力如何决定细胞形态的一个模型系统。据认为,通常呈双凹盘状的红细胞会呈现出使膜弯曲能量最小化的形状,同时受到固定面积和体积的限制。然而,最近有人提出,膜相关细胞骨架(MS)产生的剪切弹性对于解释真实红细胞的形状是必要的,尤其是那些具有高度弯曲特征的红细胞,如棘状红细胞。在这项工作中,我们通过使用理论细胞表面的球谐级数展开以及从活细胞的三维共聚焦显微镜图像估计的形状来跟踪红细胞形状变化,从而验证了这一假设。我们发现:(i)包括MS的理论模型所得到的形状与真实细胞的形状在数量上一致;(ii)通过使用尿素(使血影蛋白变性)削弱MS,会导致棘状红细胞的刺突数量在理论上预测的逐渐减少;(iii)该理论预测,MS对于稳定双凹圆盘状红细胞形态以抵抗脂质组成的变化至关重要,没有它,形状会默认变为椭圆状红细胞(双凹椭球体);(iv)我们能够通过用尿素处理健康的双凹圆盘状红细胞,诱导其采用预测的椭圆状红细胞形态。后一观察结果与血液疾病遗传性椭圆红细胞增多症和削弱细胞皮质的血影蛋白突变之间的已知联系一致。我们得出结论,虽然在没有剪切力的情况下,双凹圆盘状红细胞确实是能量最小的形状,但在健康红细胞中其稳定需要MS,并且椭圆红细胞增多症可以基于纯粹的力学考虑来解释。