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Mechanobiological induction of long-range contractility by diffusing biomolecules and size scaling in cell assemblies

机译:通过扩散生物分子和细胞组件尺寸缩放的长距离收缩力的力学诱导

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Mechanobiological studies of cell assemblies have generally focused on cells that are, in principle, identical. Here we predict theoretically the effect on cells in culture of locally introduced biochemical signals that diffuse and locally induce cytoskeletal contractility which is initially small. In steady-state, both the concentration profile of the signaling molecule as well as the contractility profile of the cell assembly are inhomogeneous, with a characteristic length that can be of the order of the system size. The long-range nature of this state originates in the elastic interactions of contractile cells (similar to long-range "macroscopic modes" in non-living elastic inclusions) and the non-linear diffusion of the signaling molecules, here termed mechanogens. We suggest model experiments on cell assemblies on substrates that can test the theory as a prelude to its applicability in embryo development where spatial gradients of morphogens initiate cellular development.
机译:细胞组件的力学研究通常集中在原则上相同的细胞上。在这里,我们预测了本地引入的生物化学信号培养的细胞对细胞的影响,该信号弥漫性和局部诱导最初小的细胞骨骼收缩性。在稳态中,信号传导分子的浓度分布以及电池组件的收缩性曲线都是不均可的,具有能够具有系统尺寸的顺序的特征长度。该状态的远程性质起源于收缩细胞的弹性相互作用(类似于非生物弹性夹杂物中的远程“宏观模式)和信号传导分子的非线性扩散,这里称为机械原。我们建议在底物上进行电池组件的模型实验,该模板可以将理论作为其在胚胎发育中的适用性的前奏,其中变形梯度发生细胞发育。

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