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Toward an in vitro vasculature: Differentiation of mesenchymal stromal cells within an endothelial cell-seeded modular construct in a microfluidic flow chamber

机译:走向体外脉管系统:微流控室中的内皮细胞播种的模块化结构内的间质基质细胞的分化。

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An in vitro tissue construct amenable to perfusion was formed by randomly packing mesenchymal stromal cell (MSC)-embedded, endothelial cell (EC)-coated collagen cylinders (modules) into a microfluidic chamber. The interstices created by the random packing of the submillimeter-sized modules created EC-lined channels. Flow caused a greater than expected amount of contraction and remodeling in the modular constructs. Flow influenced the MSC to develop smooth muscle cell markers (smooth muscle actin-positive, desmin-positive, and von Willebrand factor-negative) and migrate toward the surface of the modules. When modules were coated with EC, the extent of MSC differentiation and migration increased, suggesting that the MSC were becoming smooth muscle cell-or pericyte-like in their location and phenotype. The MSC also proliferated, resulting in a substantial increase in the number of differentiated MSC. These effects were markedly less for static controls not experiencing flow. As the MSC migrated, they created new matrix that included the deposition of proteoglycans. Collectively, these results suggest that MSC-embedded modules may be useful for the formation of functional vasculature in tissue engineered constructs. Moreover, these flow-conditioned tissue engineered constructs may be of interest as three-dimensional cell-laden platforms for drug testing and biological assays.
机译:通过将包埋了间充质基质细胞(MSC)的内皮细胞(EC)包被的胶原蛋白圆柱体(模块)随机包装到微流体腔室中,形成了适合灌注的体外组织构建体。亚毫米大小的模块的随机堆积产生的空隙产生了EC衬里通道。流动导致模块化构造中的收缩和重塑量超出预期。血流影响MSC形成平滑肌细胞标志物(平滑肌肌动蛋白阳性,结蛋白阳性和von Willebrand因子阴性)并向组件表面迁移。当模块涂有EC时,MSC分化和迁移的程度增加,这表明MSC的位置和表型正在变成平滑肌细胞或周细胞样。 MSC也增殖,导致分化的MSC数量大量增加。对于没有流动的静态对照,这些影响明显较少。随着MSC的迁移,他们创建了新的基质,其中包括蛋白聚糖的沉积。总体而言,这些结果表明,嵌入MSC的模块可能对组织工程构建体中功能性脉管系统的形成有用。此外,这些流动调节的组织工程构建体作为用于药物测试和生物学测定的三维细胞载有平台可能是令人感兴趣的。

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