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Extracellular matrix mimicking polycaprolactone-chitosan nanofibers promote stemness maintenance of mesenchymal stem cells via spheroid formation

机译:模仿聚己内酯 - 壳聚糖纳料纳料的细胞外基质促进间充质干细胞的茎秆维持通过球状形成

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The development of clinical applications has led to a perpetual increase in the demand for mesenchymal stem cells (MSCs). However, the ex vivo expansion of MSCs while maintaining their stemness and differentiation potential remains an immense challenge. MSCs require high cell density for their intercellular communication and specific physico-chemical cues from the surrounding environment for spheroid formation in order to maintain their stemness. Inadequacy of the traditional in vitro cell culture method (tissue culture plastic surface) to fulfill any of these special requirements is responsible for inducing the loss of stem cell properties of the MSCs over time. In this study, we propose that glucosaminoglycan (GAG) mimicking ultrafine nanofibers could support the spheroid culture for in vitro human MSC expansion. The geometrical and biochemical properties of nanofibers provide biomimicking cues to MSCs, as well as enhance cell-cell interactions and stimulate spheroid formation in MSCs, which subsequently result in increased cell proliferation, enhanced expression of stem cell markers and maintenance of their multilineage differentiation potential. Furthermore, close monitoring of the behavior of MSCs on nanofibers serves as the key to understand their mode of action in niche formation. Interestingly, GAG mimicking substrate stimulated MSCs for long-distance intercellular communication via 'tunneling tubes', their subsequent migration and niche formation. These kinds of cellular interactions over long distances have rarely been observed in MSCs to provide better insight for future studies on MSC niche. Furthermore, PCL-CHT nanofibers were observed to be as conducive to use as tissue culture polystyrene for stem cell expansion. Overall, these polymeric nanofibers provide a more relevant, convenient and more suitable substrate than the conventional monolayer culture for in vitro MSC expansion.
机译:临床应用的发展导致了间充质干细胞(MSCs)的需求增加。然而,MSCs的前体内扩展,同时保持其茎的茎和分化潜力仍然是一个巨大的挑战。 MSCs需要高细胞密度,用于从周围环境中的细胞间通信和特定的物理化学提示,以用于保持其茎。传统体外细胞培养方法(组织培养塑料表面)的不足,以满足这些特殊要求中的任何一种,负责诱导MSCs的干细胞性能随时间的损失。在这项研究中,我们提出了模仿超细纳米纤维的葡萄糖蛋白酶蛋白酶(GAG)可以支持体外人体MSC膨胀的球状培养物。纳米纤维的几何和生化特性为MSCs提供生物剥削提示,以及增强细胞 - 细胞相互作用并刺激MSCs中的球形形成,随后导致细胞增殖增加,增强干细胞标记物的表达和其多重分化潜力的维持。此外,密切监测MSCS对纳米纤维上的MSCs的行为用作理解其在利基地层中的作用模式的关键。有趣的是,GAG模仿衬底通过“隧道管”,其随后的迁移和Niche形成来刺激底物刺激MSC。在MSC的MSC中很少观察到这些类型的细胞相互作用,以便更好地了解未来对MSC利基的研究。此外,观察到PCL-CHT纳米纤维是有利于用作干细胞膨胀的组织培养聚苯乙烯。总的来说,这些聚合物纳米纤维提供比常规MSC膨胀的常规单层培养更相关,方便,更合适的基材。

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