Life Sciences Center, Department of Biological Models, Institute of Biochemistry, Vilnius University, LT-10257 Vilnius, Lithuania.
School of Biological Sciences, Faculty of Biology, Medicine and Health, The Univesity of Manchester, Manchester M13 9PL, UK.
Curr Issues Mol Biol. 2021 May 30;43(1):251-263. doi: 10.3390/cimb43010021.
Effective cell number monitoring throughout the three-dimensional (3D) scaffold is a key factor in tissue engineering. There are many methods developed to evaluate cell number in 2D environments; however, they often encounter limitations in 3D. Therefore, there is a demand for reliable methods to measure cell proliferation in 3D surroundings. Here, we report a novel technique for the DNA content-based evaluation of cell proliferation using DNA-binding dye DAPI. We demonstrated the method's compatibility with four different cell cultures: cancer lines MCF-7 and MH-22a, embryonic fibroblast cell line Swiss 3T3, and primary mesenchymal stem cell culture isolated from rat's incisors. The DAPI based method was able to successfully evaluate cell proliferation in 2D, 2.5D, and 3D environments. Even though the proposed method does not discriminate between viable and dead cells, it might give a convenient snapshot of the cell number at a given time point. This should help to more reliably evaluate various processes proceeding in 2.5D and 3D cultures.
有效监测整个三维(3D)支架中的细胞数量是组织工程的关键因素。已经开发出许多方法来评估 2D 环境中的细胞数量;然而,它们在 3D 中经常遇到限制。因此,需要可靠的方法来测量 3D 环境中的细胞增殖。在这里,我们报告了一种使用 DNA 结合染料 DAPI 基于 DNA 含量评估细胞增殖的新方法。我们证明了该方法与四种不同的细胞培养物的兼容性:癌细胞系 MCF-7 和 MH-22a、胚胎成纤维细胞系 Swiss 3T3 以及从大鼠门牙分离的原代间充质干细胞培养物。基于 DAPI 的方法能够成功地评估 2D、2.5D 和 3D 环境中的细胞增殖。尽管所提出的方法不能区分活细胞和死细胞,但它可以在给定时间点方便地获取细胞数量的快照。这有助于更可靠地评估 2.5D 和 3D 培养物中进行的各种过程。