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In vitro cultivation of adherent cells on microscope slides for downstream applications.
Samset Hoem, Kine; Lillerovde Ørstenvik, Hanne; Varhaugvik, Anne Elin; Tveten, Ann-Kristin.
Affiliation
  • Samset Hoem K; Department of Biological Sciences Aalesund, Faculty of Natural Sciences, Norwegian University of Science and Technology, Larsgardsvegen 2, Aalesund 6009, Norway.
  • Lillerovde Ørstenvik H; Department of Biological Sciences Aalesund, Faculty of Natural Sciences, Norwegian University of Science and Technology, Larsgardsvegen 2, Aalesund 6009, Norway.
  • Varhaugvik AE; Department of Biological Sciences Aalesund, Faculty of Natural Sciences, Norwegian University of Science and Technology, Larsgardsvegen 2, Aalesund 6009, Norway.
  • Tveten AK; Department of Biological Sciences Aalesund, Faculty of Natural Sciences, Norwegian University of Science and Technology, Larsgardsvegen 2, Aalesund 6009, Norway.
MethodsX ; 13: 102847, 2024 Dec.
Article in En | MEDLINE | ID: mdl-39101125
ABSTRACT
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.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: MethodsX Year: 2024 Document type: Article Affiliation country: Norway

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: MethodsX Year: 2024 Document type: Article Affiliation country: Norway