首页> 外文期刊>Molecular & cellular biomechanics: MCB >Structure-function relationships in the stem cell's mechanical world A: seeding protocols as a means to control shape and fate of live stem cells.
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Structure-function relationships in the stem cell's mechanical world A: seeding protocols as a means to control shape and fate of live stem cells.

机译:干细胞机械世界中的结构-功能关系A:播种协议,作为控制活干细胞形状和命运的一种手段。

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Shape and fate are intrinsic manifestations of form and function at the cell scale. Here we hypothesize that seeding density and protocol affect the form and function of live embryonic murine mesenchymal stem cells (MSCs) and their nuclei. First, the imperative for study of live cells was demonstrated in studies showing changes in cell nucleus shape that were attributable to fixation per se. Hence, we compared live cell and nuclear volume and shape between groups of a model MSC line (C3H10T1/2) seeded at, or proliferated from 5,000 cells/cm2 to one of three target densities to achieve targeted development contexts. Cell volume was shown to be dependent on initial seeding density whereas nucleus shape was shown to depend on developmental context but not seeding density. Both smaller cell volumes and flatter nuclei were found to correlate with increased expression of markers for mesenchymal condensation as well as chondrogenic and osteogenic differentiation but a decreased expression of pre-condensation and adipogenic markers. Considering the data presented here, both seeding density and protocol significantly alter the morphology of mesenchymal stem cells even at very early stages of cell culture. Thus, these design parameters may play a critical role in the success of tissue engineering strategies seeking to recreate condensation events. However, a better understanding of how these changes in cell volume and nucleus shape relate to the differentiation of MSCs is important for prescribing precise seeding conditions necessary for the development of the desired tissue type. In a companion study (Part B, following), we address the effect of concomitant volume and shape changing stresses on spatiotemporal distribution of the cytoskeletal proteins actin and tubulin. Taken together, these studies bring us one step closer to our ultimate goal of elucidating the dynamics of nucleus and cell shape change as tissue templates grow (cell proliferation) and specialize (cell differentiation).
机译:形状和命运是细胞尺度上形式和功能的内在表现。在这里我们假设播种密度和协议会影响活的胚胎鼠间充质干细胞(MSCs)及其细胞核的形式和功能。首先,在研究中证明了活细胞研究的必要性,这些研究表明细胞核形状的变化可归因于固定本身。因此,我们比较了以5,000个细胞/ cm2或从5,000个细胞/ cm2增殖到三个目标密度之一的模型MSC系(C3H10T1 / 2)的各组之间的活细胞以及核的体积和形状,以实现目标的开发环境。细胞体积显示出依赖于初始接种密度,而细胞核形状显示出依赖于发育背景而不是种子密度。发现较小的细胞体积和较平坦的核均与间充质凝集标记的表达增加,软骨形成和成骨分化有关,但预缩合和成脂标记的表达降低。考虑到此处提供的数据,即使在细胞培养的非常早期,接种密度和操作规程都会显着改变间充质干细胞的形态。因此,这些设计参数可能在寻求重建凝结事件的组织工程策略的成功中起关键作用。但是,更好地了解细胞体积和细胞核形状的这些变化如何与MSC的分化有关,对于规定所需组织类型的发育所必需的精确接种条件至关重要。在伴随研究中(下面的B部分),我们研究了伴随的体积和形状变化应力对细胞骨架蛋白肌动蛋白和微管蛋白的时空分布的影响。综上所述,这些研究使我们更接近最终目标,即阐明随着组织模板的生长(细胞增殖)和特化(细胞分化)而发生的核动力学和细胞形状变化。

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