Medical Biotechnology, Technical University of Berlin, Berlin, 13355, Germany.
Cellbricks GmbH, Berlin, 13355, Germany.
Sci Rep. 2020 Sep 24;10(1):15606. doi: 10.1038/s41598-020-72559-6.
Barrier organ models need a scaffold structure to create a two compartment culture. Technical filter membranes used most often as scaffolds may impact cell behaviour and present a barrier themselves, ultimately limiting transferability of test results. In this work we present an alternative for technical filter membrane systems: a 3D bioprinted biological membrane in 24 well format. The biological membrane, based on extracellular matrix (ECM), is highly permeable and presents a natural 3D environment for cell culture. Inspired by the human placenta we established a coculture of a trophoblast-derived cell line (BeWo b30), together with primary placental fibroblasts within the biological membrane (simulating villous stroma) and primary human placental endothelial cells-representing three cellular components of the human placental villus. All cell types maintained their cell type specific marker expression after two weeks of coculture on the biological membrane. In permeability assays the trophoblast layer developed a barrier on the biological membrane, which was even more pronounced when cocultured with fibroblasts. In this work we present a filter membrane free scaffold, we characterize its properties and assess its suitability for cell culture and barrier models. Further we show a novel placenta inspired model in a complex bioprinted coculture. In the absence of an artificial filter membrane, we demonstrate barrier architecture and functionality.
屏障器官模型需要支架结构来创建双室培养。最常被用作支架的技术滤膜可能会影响细胞行为,并形成自身的屏障,最终限制了测试结果的可转移性。在这项工作中,我们提出了技术滤膜系统的替代方案:一种 24 孔格式的 3D 生物打印生物膜。该生物膜基于细胞外基质 (ECM),具有高度的通透性,并为细胞培养提供了天然的 3D 环境。受人类胎盘的启发,我们建立了滋养层衍生细胞系 (BeWo b30) 与原代胎盘成纤维细胞在生物膜内的共培养(模拟绒毛间质)和原代人胎盘内皮细胞——代表人类胎盘绒毛的三个细胞成分。所有细胞类型在生物膜上共培养两周后,均保持其细胞类型特异性标志物的表达。在通透性测定中,滋养层在生物膜上形成了屏障,当与成纤维细胞共培养时,这种屏障更为明显。在这项工作中,我们提出了一种无滤膜支架,对其特性进行了表征,并评估了其用于细胞培养和屏障模型的适用性。此外,我们还展示了一种新型基于胎盘的复杂生物打印共培养模型。在没有人工滤膜的情况下,我们证明了屏障结构和功能的存在。