Fraunhofer Institute for Silicate Research ISC, Neunerplatz 2, 97082, Würzburg, Germany.
Julius-Maximilians-Universität Würzburg, Chemical Technology of Material Synthesis, Röntgenring 11, 97070, Würzburg, Germany.
Adv Biol (Weinh). 2021 Jul;5(7):e2000570. doi: 10.1002/adbi.202000570. Epub 2021 May 7.
The introduction of novel bioactive materials to manipulate living cell behavior is a crucial topic for biomedical research and tissue engineering. Biomaterials or surface patterns that boost specific cell functions can enable innovative new products in cell culture and diagnostics. This study investigates the influence of the intrinsically nano-patterned surface of nanoporous glass membranes on the behavior of mammalian cells. Three different cell lines and primary human mesenchymal stem cells (hMSCs) proliferate readily on nanoporous glass membranes with mean pore sizes between 10 and 124 nm. In both proliferation and mRNA expression experiments, L929 fibroblasts show a distinct trend toward mean pore sizes >80 nm. For primary hMSCs, excellent proliferation is observed on all nanoporous surfaces. hMSCs on samples with 17 nm pore size display increased expression of COL10, COL2A1, and SOX9, especially during the first two weeks of culture. In the upside down culture, SK-MEL-28 cells on nanoporous glass resist the gravitational force and proliferate well in contrast to cells on flat references. The effect of paclitaxel treatment of MDA-MB-321 breast cancer cells is already visible after 48 h on nanoporous membranes and strongly pronounced in comparison to reference samples, underlining the material's potential for functional drug screening.
将新型生物活性材料引入来操控活细胞行为是生物医学研究和组织工程的一个关键课题。能够促进特定细胞功能的生物材料或表面图案,可以为细胞培养和诊断学带来创新的新产品。本研究调查了纳米多孔玻璃膜固有纳米图案表面对哺乳动物细胞行为的影响。三种不同的细胞系和原代人骨髓间充质干细胞(hMSCs)在孔径为 10 至 124nm 的纳米多孔玻璃膜上迅速增殖。在增殖和 mRNA 表达实验中,L929 成纤维细胞对大于 80nm 的平均孔径表现出明显的趋势。对于原代 hMSCs,所有纳米多孔表面都表现出良好的增殖。在孔径为 17nm 的样品上,hMSCs 表达 COL10、COL2A1 和 SOX9 的水平升高,尤其是在培养的头两周。在倒置培养中,SK-MEL-28 细胞在纳米多孔玻璃上能够抵抗重力并良好增殖,与在平面对照上的细胞相比有明显差异。纳米多孔膜上紫杉醇处理 MDA-MB-321 乳腺癌细胞 48 小时后即可观察到效果,与对照样品相比效果明显,突出了该材料在功能药物筛选方面的潜力。