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2D and 3D-Organized Cardiac Cells Shows Differences in Cellular Morphology, Adhesion Junctions, Presence of Myofibrils and Protein Expression

机译:2D和3D组织的心脏细胞在细胞形态,粘附连接,肌原纤维的存在和蛋白质表达方面显示差异

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摘要

Cardiac cells are organized in vivo in a complex tridimensional structural organization that is crucial for heart function. While in vitro studies can reveal details about cardiac cell biology, usually cells are grown on simplified two-dimensional (2D) environments. To address these differences, we established a cardiac cell culture composed of both 2D and three-dimensional (3D)-organized cells. Our results shows significant differences between the two culture contexts in relation to the overall morphology of the cells, contraction ability, proliferation rate, presence of intercellular adhesion structures, organization of myofibrils, mitochondria morphology, endoplasmic reticulum contents, cytoskeletal filaments and extracellular matrix distribution, and expression of markers of cardiac differentiation. Cardiac cells grown in 2D-context displayed a flattened and well spread shape, were mostly isolated and their cytoplasm was filled with a large network of microfilaments and microtubules. In contrast, 3D-cells were smaller in size, were always in close contact with each other with several cellular junctions, and displayed a less conspicuous cytoskeletal network. 3D-cells had more mitochondria and myofibrils and these cells contract spontaneously more often than 2D-cells. On the other hand, endoplasmic reticulum membranes were present in higher amounts in 2D-cells when compared to 3D-cells. The expression of desmin, cadherin and alpha-actinin was higher in 3D-aggregates compared to 2D-spread cells. These findings indicate that the tridimensional environment in which the cardiac cells are grown influence several aspects of cardiac differentiation, including cell adhesion, cell shape, myofibril assembly, mitochondria contents and protein expression. We suggest that the use of this cardiac culture model, with 2D and 3D-context cells, could be useful for studies on the effects of different drugs, or growth factors, giving valuable information on the biological response of cells grown in different spatial organizations.
机译:心脏细胞在体内以对心脏功能至关重要的复杂三维结构组织起来。尽管体外研究可以揭示有关心脏细胞生物学的细节,但通常细胞是在简化的二维(2D)环境中生长的。为了解决这些差异,我们建立了由2D和三维(3D)组织的细胞组成的心脏细胞培养物。我们的结果表明,两种培养背景之间的差异很大,包括细胞的总体形态,收缩能力,增殖率,细胞间粘附结构的存在,肌原纤维的组织,线粒体形态,内质网含量,细胞骨架细丝和细胞外基质分布,和心脏分化标志物的表达。在2D环境中生长的心肌细胞显示出扁平且分布良好的形状,大部分被分离,并且其细胞质充满了微丝和微管的大型网络。相比之下,3D细胞的尺寸较小,始终通过数个细胞接头彼此紧密接触,并且显示的细胞骨架网络不那么明显。 3D细胞具有更多的线粒体和肌原纤维,并且这些细胞比2D细胞更容易自发收缩。另一方面,与3D细胞相比,内质网膜在2D细胞中的含量更高。与2D扩散细胞相比,3D聚集体中desmin,钙粘着蛋白和α-肌动蛋白的表达更高。这些发现表明,心肌细胞在其中生长的三维环境影响了心脏分化的几个方面,包括细胞粘附,细胞形状,肌原纤维组装,线粒体含量和蛋白质表达。我们建议将这种带有2D和3D上下文细胞的心脏培养模型用于研究不同药物或生长因子的作用,从而为在不同空间组织中生长的细胞的生物学反应提供有价值的信息。

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