Tsuboi Alice, Umetsu Daiki, Kuranaga Erina, Fujimoto Koichi
Laboratory of Theoretical Biology, Department of Biological Sciences, Osaka UniversityToyonaka, Japan.
Laboratory of Histogenetic Dynamics, Graduate School of Life Sciences, Tohoku UniversitySendai, Japan.
Front Cell Dev Biol. 2017 Aug 3;5:68. doi: 10.3389/fcell.2017.00068. eCollection 2017.
Cell populations in multicellular organisms show genetic and non-genetic heterogeneity, even in undifferentiated tissues of multipotent cells during development and tumorigenesis. The heterogeneity causes difference of mechanical properties, such as, cell bond tension or adhesion, at the cell-cell interface, which determine the shape of clonal population boundaries via cell sorting or mixing. The boundary shape could alter the degree of cell-cell contacts and thus influence the physiological consequences of sorting or mixing at the boundary (e.g., tumor suppression or progression), suggesting that the cell mechanics could help clarify the physiology of heterogeneous tissues. While precise inference of mechanical tension loaded at each cell-cell contacts has been extensively developed, there has been little progress on how to distinguish the population-boundary geometry and identify the cause of geometry in heterogeneous tissues. We developed a pipeline by combining multivariate analysis of clone shape with tissue mechanical simulations. We examined clones with four different genotypes within wing imaginal discs: wild-type, () overexpression, () overexpression, and RNAi. Although the clones were previously known to exhibit smoothed or convoluted morphologies, their mechanical properties were unknown. By applying a multivariate analysis to multiple criteria used to quantify the clone shapes based on individual cell shapes, we found the optimal criteria to distinguish not only among the four genotypes, but also non-genetic heterogeneity from genetic one. The efficient segregation of clone shape enabled us to quantitatively compare experimental data with tissue mechanical simulations. As a result, we identified the mechanical basis contributed to clone shape of distinct genotypes. The present pipeline will promote the understanding of the functions of mechanical interactions in heterogeneous tissue in a non-invasive manner.
多细胞生物中的细胞群体表现出遗传和非遗传异质性,即使在发育和肿瘤发生过程中多能细胞的未分化组织中也是如此。这种异质性导致细胞-细胞界面处机械特性的差异,如细胞键张力或粘附力,这些特性通过细胞分选或混合决定克隆群体边界的形状。边界形状可以改变细胞-细胞接触的程度,从而影响边界处分选或混合的生理后果(例如,肿瘤抑制或进展),这表明细胞力学有助于阐明异质组织的生理学。虽然已经广泛发展了对每个细胞-细胞接触处加载的机械张力的精确推断,但在如何区分群体边界几何形状以及确定异质组织中几何形状的原因方面进展甚微。我们通过将克隆形状的多变量分析与组织力学模拟相结合,开发了一个流程。我们在翅成虫盘内检查了具有四种不同基因型的克隆:野生型、()过表达、()过表达和RNA干扰。尽管这些克隆以前已知表现出平滑或卷曲的形态,但其机械特性尚不清楚。通过对基于单个细胞形状量化克隆形状的多个标准进行多变量分析,我们找到了不仅能区分四种基因型,还能区分非遗传异质性和遗传异质性的最佳标准。克隆形状的有效分离使我们能够将实验数据与组织力学模拟进行定量比较。结果,我们确定了导致不同基因型克隆形状的机械基础。本流程将以非侵入性方式促进对异质组织中机械相互作用功能的理解。