Aucamp Janine, Calitz Carlemi, Bronkhorst Abel J, Wrzesinski Krzysztof, Hamman Sias, Gouws Chrisna, Pretorius Piet J
Human Metabolomics, North-West University, Private Bag X6001, Potchefstroom, 2520, South Africa.
Centre of Excellence for Pharmaceutical Sciences, North-West University, Private Bag X6001, Potchefstroom, 2520, South Africa.
Int J Biochem Cell Biol. 2017 Aug;89:182-192. doi: 10.1016/j.biocel.2017.06.014. Epub 2017 Jun 24.
Investigating the biological functions of cell-free DNA (cfDNA) is limited by the interference of vast numbers of putative sources and causes of DNA release into circulation. Utilization of three-dimensional (3D) spheroid cell cultures, models with characteristics closer to the in vivo state, may be of significant benefit for cfDNA research.
CfDNA was isolated from the growth medium of C3A spheroid cultures in rotating bioreactors during both normal growth and treatment with acetaminophen. Spheroid growth was monitored via planimetry, lactate dehydrogenase activity and glucose consumption and was related to isolated cfDNA characteristics.
Changes in spheroid growth and stability were effectively mirrored by cfDNA characteristics. CfDNA characteristics correlated with that of previous two-dimensional (2D) cell culture and human plasma research.
3D spheroid cultures can serve as effective, simplified in vivo-simulating "closed-circuit" models since putative sources of cfDNA are limited to only the targeted cells. In addition, cfDNA can also serve as an alternative or auxiliary marker for tracking spheroid growth, development and culture stability.
3D cell cultures can be used to translate "closed-circuit" in vitro model research into data that is relevant for in vivo studies and clinical applications. In turn, the utilization of cfDNA during 3D culture research can optimize sample collection without affecting the stability of the growth environment. Combining 3D culture and cfDNA research could, therefore, optimize both research fields.
循环中无细胞DNA(cfDNA)的大量假定来源和DNA释放原因干扰了对其生物学功能的研究。利用三维(3D)球体细胞培养,这种更接近体内状态的模型,可能对cfDNA研究有显著益处。
在正常生长和用对乙酰氨基酚处理期间,从旋转生物反应器中C3A球体培养物的生长培养基中分离cfDNA。通过平面测量法、乳酸脱氢酶活性和葡萄糖消耗监测球体生长,并将其与分离的cfDNA特征相关联。
cfDNA特征有效反映了球体生长和稳定性的变化。cfDNA特征与先前二维(2D)细胞培养和人血浆研究的特征相关。
3D球体培养可作为有效、简化且模拟体内的“闭路”模型,因为cfDNA的假定来源仅限于目标细胞。此外,cfDNA还可作为跟踪球体生长、发育和培养稳定性的替代或辅助标志物。
3D细胞培养可用于将“闭路”体外模型研究转化为与体内研究和临床应用相关的数据。反过来,在3D培养研究中利用cfDNA可优化样本采集,而不影响生长环境的稳定性。因此,将3D培养和cfDNA研究相结合可优化这两个研究领域。