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Long term morphological characterization of mesenchymal stromal cells 3D spheroids built with a rapid method based on entry-level equipment

机译:基于入门级设备的快速方法构建的间充质基质细胞3D球体的长期形态表征

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摘要

Three-dimensional (3D) spheroids of mesenchymal stromal cells (MSC) have been demonstrated to improve a wide range of MSC features, such as multilineage potential, secretion of therapeutic factors, and resistance against hypoxic condition. Accordingly, they represent a promising tool in regenerative medicine for several biological and clinical applications. Many approaches have been proposed to generate MSC spheroids. They usually require specific generation systems, such as rotatory bioreactors or low-attachment plates, and each approach has its own disadvantages. Furthermore, an over-time analysis of morphological homogeneity and architectural stability of the spheroids generated is rarely provided. In this work we adapted the “pellet culture” method to obtain homogenous spheroids of MSC and maintain them in vitro for long term studies. We analysed their outer and inner structure over a 2-month period to provide morphological and architectural information regarding the spheroids generated. Quantitative and qualitative data were obtained using brightfield and confocal microscope imaging coupled to a computational analysis to estimate volume, sphericity, and jagging degree. In addition, histological evaluation was performed to more thoroughly assess the cellular composition and the internal architecture of the 3D spheroids. The results provided show that MSC spheroids generated with the proposed approach are homogeneous and stable, from both morphological and architectural points of view, for a period of at least 15 days, approximately between day 15 and day 30 after their generation. Accordingly, the approach proposed serves as a rapid, cost-effective, and efficient method to generate and maintain MSC spheroids using common entry-level laboratory equipment only.
机译:间充质基质细胞(MSC)的三维(3D)球体已被证明可以改善MSC的多种功能,例如多谱系潜能,治疗因子的分泌以及对低氧状态的抵抗力。因此,它们代表了在再生医学中用于多种生物学和临床应用的有前途的工具。已经提出了许多方法来产生MSC球体。他们通常需要特定的生成系统,例如旋转生物反应器或低附着平板,并且每种方法都有其自身的缺点。此外,很少提供对生成的球体的形态均匀性和结构稳定性的超时分析。在这项工作中,我们采用“丸培养”方法获得了MSC的均匀球体,并在体外对其进行了长期研究。我们在两个月的时间内分析了它们的外部和内部结构,以提供有关所产生的球体的形态和建筑信息。使用明场和共聚焦显微镜成像以及计算分析来估计体积,球形度和锯齿度,可以获得定量和定性数据。此外,进行了组织学评估,以更彻底地评估3D球体的细胞组成和内部结构。所提供的结果表明,从形态学和建筑学的角度来看,通过提出的方法生成的MSC球体在生成后大约15天到30天之间至少15天的时间是均匀且稳定的。因此,所提出的方法是仅使用普通入门级实验室设备来生成和维护MSC球体的一种快速,经济高效的方法。

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