Ugrin Milena, Dinic Jelena, Jeremic Sanja, Dragicevic Sandra, Banovic Djeri Bojana, Nikolic Aleksandra
Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, Vojvode Stepe 444A, 11042 Belgrade, Serbia.
Department of Neurobiology, Institute for Biological Research "Sinisa Stankovic"-National Institute of Republic of Serbia, University of Belgrade, Bulevar Despota Stefana 142, 11060 Belgrade, Serbia.
Nanomaterials (Basel). 2021 Sep 7;11(9):2322. doi: 10.3390/nano11092322.
Bacterial nanocellulose (BNC) stands out among polymers as a promising biomaterial due to its mechanical strength, hydrophilicity, biocompatibility, biodegradability, low toxicity and renewability. The use of scaffolds based on BNC for 3D cell culture has been previously demonstrated. The study exploited excellent properties of the BNC to develop an efficient and low-cost in vitro cell migration assay. The BNC scaffold was introduced into a cell culture 24 h after the SW480 cells were seeded, and cells were allowed to enter the scaffold within the next 24-48 h. The cells were stained with different fluorophores either before or after the introduction of the scaffold in the culture. Untreated cells were observed to enter the BNC scaffold in significant numbers, form clusters and retain a high viability after 48 h. To validate the assay's usability for drug development, the treatments of SW480 cells were performed using aspirin, an agent known to reduce the migratory potential of this cell line in culture. This study demonstrates the application of BNC as a scaffold for cell migration testing as a low-cost alternative to commercial assays based on the Boyden chamber principle. The assay could be further developed for routine use in cancer research and anticancer drug development.
细菌纳米纤维素(BNC)作为一种有前途的生物材料,在聚合物中脱颖而出,这得益于其机械强度、亲水性、生物相容性、可生物降解性、低毒性和可再生性。此前已有研究证明基于BNC的支架可用于三维细胞培养。该研究利用BNC的优异特性开发了一种高效且低成本的体外细胞迁移测定方法。在接种SW480细胞24小时后,将BNC支架引入细胞培养物中,并在接下来的24至48小时内让细胞进入支架。在将支架引入培养物之前或之后,用不同的荧光团对细胞进行染色。观察到未经处理的细胞大量进入BNC支架,形成簇,并在48小时后保持高活力。为了验证该测定方法在药物开发中的可用性,使用阿司匹林对SW480细胞进行处理,阿司匹林是一种已知可降低该细胞系在培养物中迁移潜力的药物。本研究证明了BNC作为细胞迁移测试支架的应用,是基于博伊登室原理的商业测定方法的低成本替代方案。该测定方法可进一步开发用于癌症研究和抗癌药物开发的常规用途。