Samset Hoem Kine, Lillerovde Ørstenvik Hanne, Varhaugvik Anne Elin, Tveten Ann-Kristin
Department of Biological Sciences Aalesund, Faculty of Natural Sciences, Norwegian University of Science and Technology, Larsgardsvegen 2, Aalesund 6009, Norway.
MethodsX. 2024 Jul 5;13:102847. doi: 10.1016/j.mex.2024.102847. eCollection 2024 Dec.
In vitro studies with cultured cells are often conducted as an important part of basic research. Adherent cells are typically cultivated in flasks or trays, for which cell staining and subsequent visualization become impractical. We here present a simple step-by-step method for growing adherent cells directly on glass microscope slides, using low-cost equipment readily available in most laboratories. Most parameters such as type of microscope slide (e.g. surface coating), cell seeding concentrations and incubation times can be adjusted according to cell line characteristics and experimental aims, reflecting the methods' flexibility. Through our experiments, microscope slides proved to provide an acceptable surface for cell adhesion and growth of the tested cell lines, as well as being robust and functional with respect to downstream procedures. The method can potentially be combined with different techniques for visualization of experimental effects, such as histological staining methods, fluorescent staining, and immunochemistry. In our method development we have successfully cultivated three different cell lines directly on microscope slides - Atlantic salmon kidney cells (ASK), rainbow trout gill cells (RTgill-W1), and human cancerous lung cells (A549) - and subjected them to various experimental treatments. Finally, as proof-of-concept we provide examples of successful histological staining of the fixed cells. Experimental design in short:•Cultivate cells and calculate cell concentration•Seed a small volume of growth medium with an appropriate number of cells on microscope slide in an area confined by hydrophobic marker•Let cells adhere over night before adding more growth medium or directly conducting experiments and fixing cells for downstream applications.
使用培养细胞进行的体外研究通常是基础研究的重要组成部分。贴壁细胞通常在培养瓶或培养皿中培养,而细胞染色及后续的观察在这种情况下变得不切实际。我们在此介绍一种简单的分步方法,可使用大多数实验室都容易获得的低成本设备,将贴壁细胞直接培养在玻璃显微镜载玻片上。诸如显微镜载玻片类型(例如表面涂层)、细胞接种浓度和孵育时间等大多数参数都可以根据细胞系特征和实验目的进行调整,这体现了该方法的灵活性。通过我们的实验,显微镜载玻片被证明能为受试细胞系提供可接受的细胞黏附及生长表面,并且在下游实验步骤中表现稳定且功能良好。该方法有可能与不同的实验效果可视化技术相结合,如组织学染色方法、荧光染色和免疫化学。在我们的方法开发过程中,我们已成功地将三种不同的细胞系直接培养在显微镜载玻片上——大西洋鲑鱼肾细胞(ASK)、虹鳟鱼鳃细胞(RTgill-W1)和人肺癌细胞(A549)——并对它们进行了各种实验处理。最后,作为概念验证,我们提供了固定细胞成功进行组织学染色的示例。简要实验设计:•培养细胞并计算细胞浓度•在由疏水标记物限定的区域内,将适量细胞接种于少量生长培养基中,滴加在显微镜载玻片上•让细胞过夜贴壁,然后再添加更多生长培养基,或直接进行实验并固定细胞以用于下游应用。