Department of Instructive Biomaterials Engineering, MERLN Institute for Technology-Inspired Regenerative Medicine, Maastricht University, P.O. Box 616, 6200 MD Maastricht, The Netherlands.
ACS Appl Mater Interfaces. 2024 Apr 10;16(14):17347-17360. doi: 10.1021/acsami.4c02321. Epub 2024 Apr 1.
Three-dimensional (3D) cell assemblies, such as multicellular spheroids, can be powerful biological tools to closely mimic the complexity of cell-cell and cell-matrix interactions in a native-like microenvironment. However, potential applications of large spheroids are limited by the insufficient diffusion of oxygen and nutrients through the spheroids and, thus, result in the formation of a necrotic core. To overcome this drawback, we present a new strategy based on nanoparticle-coated microparticles. In this study, microparticles function as synthetic centers to regulate the diffusion of small molecules, such as oxygen and nutrients, within human mesenchymal stem cell (hMSC) spheroids. The nanoparticle coating on the microparticle surface acts as a nutrient reservoir to release glucose locally within the spheroids. We first coated the surface of the poly(lactic--glycolic acid) (PLGA) microparticles with mesoporous silica nanoparticles (MSNs) based on electrostatic interactions and then formed cell-nanofunctionalized microparticle spheroids. Next, we investigated the stability of the MSN coating on the microparticles' surface during 14 days of incubation in cell culture medium at 37 °C. Then, we evaluated the influence of MSN-coated PLGA microparticles on spheroid aggregation and cell viability. Our results showed the formation of homogeneous spheroids with good cell viability. As a proof of concept, fluorescently labeled glucose (2-NBD glucose) was loaded into the MSNs at different concentrations, and the release behavior was monitored. For cell culture studies, glucose was loaded into the MSNs coated onto the PLGA microparticles to sustain local nutrient release within the hMSC spheroids. results demonstrated that the local delivery of glucose from MSNs enhanced the cell viability in spheroids during a short-term hypoxic culture. Taken together, the newly developed nanofunctionalized microparticle-based delivery system may offer a versatile platform for local delivery of small molecules within 3D cellular assemblies and, thus, improve cell viability in spheroids.
三维(3D)细胞组装体,如多细胞球体,可以成为强大的生物工具,能够在类似于天然的微环境中紧密模拟细胞-细胞和细胞-基质相互作用的复杂性。然而,大球体的潜在应用受到球体中氧气和营养物质扩散不足的限制,从而导致坏死核心的形成。为了克服这一缺点,我们提出了一种基于纳米颗粒涂层微球的新策略。在这项研究中,微球作为合成中心,调节人间充质干细胞(hMSC)球体中小分子(如氧气和营养物质)的扩散。微球表面的纳米颗粒涂层作为营养物质的储存库,在球体内部局部释放葡萄糖。我们首先基于静电相互作用在聚(乳酸-羟基乙酸)(PLGA)微球表面涂覆介孔硅纳米颗粒(MSNs),然后形成细胞纳米功能化微球球体。接下来,我们研究了在 37°C 细胞培养基中孵育 14 天时 MSN 在微球表面的稳定性。然后,我们评估了 MSN 涂层 PLGA 微球对球体聚集和细胞活力的影响。结果表明,形成了具有良好细胞活力的均匀球体。作为概念验证,将荧光标记的葡萄糖(2-NBD 葡萄糖)以不同浓度载入 MSNs,并监测其释放行为。对于细胞培养研究,将葡萄糖载入涂覆在 PLGA 微球上的 MSNs 中,以维持 hMSC 球体内部的局部营养物质释放。结果表明,MSNs 局部递送葡萄糖可增强短期低氧培养期间球体中的细胞活力。总之,新开发的基于纳米功能化微球的递药系统可为 3D 细胞组装体中小分子的局部递送提供一个多功能平台,从而提高球体中的细胞活力。