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Theoretical tool bridging cell polarities with development of robust morphologies

机译:理论工具弥合细胞极性与稳健形态的发展

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摘要

Despite continual renewal and damages, a multicellular organism is able to maintain its complex morphology. How is this stability compatible with the complexity and diversity of living forms? Looking for answers at protein level may be limiting as diverging protein sequences can result in similar morphologies. Inspired by the progressive role of apical-basal and planar cell polarity in development, we propose that stability, complexity, and diversity are emergent properties in populations of proliferating polarized cells. We support our hypothesis by a theoretical approach, developed to effectively capture both types of polar cell adhesions. When applied to specific cases of development – gastrulation and the origins of folds and tubes – our theoretical tool suggests experimentally testable predictions pointing to the strength of polar adhesion, restricted directions of cell polarities, and the rate of cell proliferation to be major determinants of morphological diversity and stability.
机译:尽管不断更新和破坏,但多细胞生物仍能够保持其复杂的形态。这种稳定性如何与生活形式的复杂性和多样性兼容?在蛋白质水平上寻找答案可能会受到限制,因为差异的蛋白质序列会导致相似的形态。受顶基和平面细胞极性在发育中的逐步作用的启发,我们提出稳定性,复杂性和多样性是激增极化细胞群体中的新兴特性。我们通过理论方法来支持我们的假设,该理论方法被开发为有效捕获两种类型的极性细胞粘附。当应用于发育的特定情况时-胃形成以及褶皱和小管的起源-我们的理论工具提出了实验可测试的预测,这些预测指出极性粘附的强度,细胞极性的受限制方向以及细胞增殖的速率是形态学的主要决定因素多样性和稳定性。

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