Gilbert Daniel F, Mofrad Sepideh Abolpour, Friedrich Oliver, Wiest Joachim
Institute of Medical Biotechnology, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.
Erlangen Graduate School in Advanced Optical Technologies (SAOT), Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.
Cytotechnology. 2019 Feb;71(1):443-452. doi: 10.1007/s10616-018-0263-z. Epub 2018 Dec 4.
In vitro culture models have become an indispensable tool for assessing a vast variety of biological questions in many scientific fields. However, common in vitro cultures are maintained under static conditions, which do not reflect the in vivo situation and create a non-physiological environment. To assess whether the growth characteristics of cells cultured at pulsed-perfused versus static conditions differ, we observed the growth of differentially cultured cells in vitro by life-cell time-lapse imaging of recombinant HEK293 cells, stably expressing yellow fluorescent protein. Cells were grown for ~ 30 h at 37 °C and ambient CO concentration in biochips mounted into a custom-designed 3D printed carrier and were imaged at a rate of ten images per hour using a fluorescence microscope with environment control infrastructure. Cells in one chip were maintained under static conditions whereas cells in another chip were recurrently perfused with fresh media. Generated image series were quantitatively analyzed using a custom-modified cell detection software. Imaging data averaged from four biological replicates per culturing condition demonstrate that cells cultured under conventional conditions exhibit an exponential growth rate. In contrast, cells cultured in periodic mode exhibited a non-exponential growth rate. Our data clearly indicate differential growth characteristics of cells cultured under periodic versus static conditions highlighting the impact of the culture conditions on the physiology of cells in vitro.
体外培养模型已成为评估许多科学领域中各种生物学问题不可或缺的工具。然而,常见的体外培养是在静态条件下进行的,这无法反映体内情况,且会创造出非生理环境。为了评估在脉冲灌注与静态条件下培养的细胞的生长特性是否不同,我们通过对稳定表达黄色荧光蛋白的重组HEK293细胞进行活细胞延时成像,观察了体外不同培养条件下细胞的生长情况。将细胞在37°C和环境CO浓度下,在安装于定制设计的3D打印载体中的生物芯片中培养约30小时,并使用具有环境控制基础设施的荧光显微镜以每小时十张图像的速率进行成像。一个芯片中的细胞保持在静态条件下,而另一个芯片中的细胞则反复用新鲜培养基灌注。使用定制修改的细胞检测软件对生成的图像序列进行定量分析。每个培养条件下四个生物学重复的成像数据平均值表明,在传统条件下培养的细胞呈现指数生长速率。相比之下,以周期性模式培养的细胞呈现非指数生长速率。我们的数据清楚地表明了在周期性与静态条件下培养的细胞具有不同的生长特性,突出了培养条件对体外细胞生理学的影响。