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细胞脱离动力学:离散受体簇的剥离

Kinetics of cell detachment: peeling of discrete receptor clusters.

作者信息

Ward M D, Dembo M, Hammer D A

机构信息

School of Chemical Engineering, Cornell University, Ithaca, New York 14853.

出版信息

Biophys J. 1994 Dec;67(6):2522-34. doi: 10.1016/S0006-3495(94)80742-8.

Abstract

Clustering of cell surface adhesion receptors is an essential step in the development of focal contacts, specialized cell-substrate attachment sites where receptors are simultaneously linked to extracellular ligand and cytoskeletal proteins. Previously, we examined the effect of receptor clustering on attachment strength. Here, we employ the numerical methodology developed by Dembo and colleagues (Dembo, M., D.C. Torney, K. Saxman, and D. Hammer. 1988. Proc. R. Soc. Lond. B. 234:55-83) to investigate the kinetics of cell detachment when receptors are clustered into discrete patches. We show that the membrane peeling velocity decreases if receptors are clustered within a patch located inside the contact region. Peeling of clusters is influenced by the chemistry and mechanics of receptor-ligand bonds within the patch. Detachment is also prohibited if the applied tension equals the critical tension of the patch, unless the patch length is small compared with the boundary length over which membrane bending occurs, in which case the patch will peel. Peeling of these short patches only occurs when the mechanical stiffness of clustered bonds is within an optimal range. We compare our model predictions with experimental measurements of T lymphocyte detachment from ICAM-1 substrates. We demonstrate that if discrete patches of receptors are present, detachment occurs through intervals of slow and fast peeling, similar to the dynamics of T lymphocyte peeling, indicating that clustering of LFA-1 receptors is one possible explanation for the observed detachment kinetics in this system.

摘要

细胞表面黏附受体的聚集是黏着斑形成过程中的关键步骤,黏着斑是一种特殊的细胞-基质附着位点,在此位点受体同时与细胞外配体及细胞骨架蛋白相连。此前,我们研究了受体聚集对附着强度的影响。在此,我们采用Dembo及其同事开发的数值方法(Dembo, M., D.C. Torney, K. Saxman, and D. Hammer. 1988. Proc. R. Soc. Lond. B. 234:55 - 83)来研究当受体聚集成离散斑块时细胞脱离的动力学。我们发现,如果受体在位于接触区域内的斑块中聚集,膜剥离速度会降低。斑块的剥离受斑块内受体-配体键的化学性质和力学性质影响。如果施加的张力等于斑块的临界张力,脱离也会受到抑制,除非斑块长度与发生膜弯曲的边界长度相比很小,在这种情况下斑块会剥离。只有当聚集键的机械刚度处于最佳范围内时,这些短斑块才会发生剥离。我们将模型预测结果与T淋巴细胞从ICAM - 1底物上脱离的实验测量结果进行比较。我们证明,如果存在离散的受体斑块,脱离会通过缓慢和快速剥离的间隔发生,这与T淋巴细胞剥离的动力学相似,表明LFA - 1受体的聚集是该系统中观察到的脱离动力学的一种可能解释。

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