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Patterns of periodic holes created by increased cell motility

机译:由于细胞运动性增强而形成的周期性空洞模式

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摘要

The reaction and diffusion of morphogens is a mechanism widely used to explain many spatial patterns in physics, chemistry and developmental biology. However, because experimental control is limited in most biological systems, it is often unclear what mechanisms account for the biological patterns that arise. Here, we study a biological model of cultured vascular mesenchymal cells (VMCs), which normally self-organize into aggregates that form into labyrinthine configurations. We use an experimental control and a mathematical model that includes reacting and diffusing morphogens and a third variable reflecting local cell density. With direct measurements showing that cell motility was increased ninefold and threefold by inhibiting either Rho kinase or non-muscle myosin-II, respectively, our experimental results and mathematical modelling demonstrate that increased motility alters the multicellular pattern of the VMC cultures, from labyrinthine to a pattern of periodic holes. These results suggest implications for the tissue engineering of functional replacements for trabecular or spongy tissue such as endocardium and bone.
机译:形态发生子的反应和扩散是一种广泛用于解释物理学,化学和发育生物学中许多空间模式的机制。但是,由于大多数生物系统中的实验控制都受到限制,因此通常不清楚哪种机制解释了所出现的生物模式。在这里,我们研究了培养的血管间充质细胞(VMC)的生物学模型,该细胞通常自组织成聚集体,形成迷宫状构型。我们使用实验控制和数学模型,其中包括反应和扩散吗啡原和反映局部细胞密度的第三个变量。通过直接测量显示,通过抑制Rho激酶或非肌肉肌球蛋白II,细胞运动分别增加了9倍和3倍,我们的实验结果和数学模型表明,增加的运动能力改变了VMC培养物的多细胞模式,从迷宫型变为细胞型。周期性孔的样式。这些结果表明对小梁或海绵状组织(例如心内膜和骨)的功能性替代的组织工程意义。

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