Abstract

BackgroundThree dimensional (3D) cell cultures have been an area of increasing interest and relevance across several research fields including drug discovery, developmental biology and stem cell-based therapies. However, handling 3D structures can be difficult. In particular, the replacement of liquid media and reagents in which liquid is removed using pipettes is difficult to perform as the 3D spheroids can be easily aspirated into the pipette tip.ResultsWe have developed the 3D-tip, a novel tool that facilitates media change and washing procedures of 3D-spheroid cultures. The 3D-tip contains a mesh with 40-μm pores allowing the aspiration of liquids including media, drugs, buffers and reagents, with the mesh acting as a barrier preventing the spheroids being aspirated into the pipette tip. After aspiration of liquids, the spheroids are gently deposited back into the culture vessel. Our results demonstrate that the 3D-tips offer superior handling of 3D-spheroid cultures in comparison to commonly used methods. We showed that the 3D-tips can easily be used on both fixed and unfixed spheroids and on cancer cell, stem cell and glial cell spheroids.In contrast with the 50/50 media exchange method, the 3D-tips allow a complete media change with minimal loss of spheroids and without damaging their morphology. Our results showed that 86.0% of spheroids remained in the chamber after changing the media using the 3D-tips. In contrast, only 45.0% of spheroids remained using the 50/50 media exchange strategy.In comparison with the centrifugation technique, the 3D-tips preserved spheroids whereas centrifugation led to the loss of spheroids and/or the alteration of the size and shape of the 3D cellular structures. We observed that 87.6 and 84.6% of the fixed and unfixed spheroids remained using the 3D-tip, respectively. In contrast, only 66.3% of the fixed spheroids and 36.4% of the unfixed spheroids were left using the centrifugation method. From a time perspective, the 3D-tips dramatically reduce the time taken for replacing media.ConclusionsThis novel pipette tip is suitable for high throughput screening and automation and will revolutionise the techniques used for the production and analysis of 3D spheroids.

Highlights

  • Three dimensional (3D) cell culture has led a revolution in eukaryotic cell culture

  • The 3D-tip is suitable for liquid handling with live 3D cell spheroids Three-dimensional cell cultures of olfactory ensheathing cells (OECs) were generated in naked liquid marbles (NLMs) [6] and transferred into an 8-well chamber

  • Removal of the liquid medium is needed for several different processes including refreshing culture medium, adding specific reagents for assays, and replacing with fixative solution

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Summary

Results

The 3D-tip is suitable for liquid handling with live (unfixed) 3D cell spheroids Three-dimensional cell cultures of olfactory ensheathing cells (OECs) were generated in naked liquid marbles (NLMs) [6] and transferred into an 8-well chamber. We observed that on average 86.0% of spheroids remained in the chamber after changing the media using the 3D-tips (Fig. 2a and b). A comparative study between the 3D-tip system and the commonly used centrifugation method for fluorescence microscopy was performed in parallel using fixed 3D cell spheroids. Comparative study between the 3D-tip method and the centrifugation technique for fluorescence labelling of live (unfixed) 3D cell spheroids Labelling of live cells is often routinely performed with a range of different stains. We performed a comparative study between the 3D-tip system and the commonly used centrifugation method for staining live (unfixed) cell spheroids. 84.6% of spheroids remained using the 3D-tip while, in contrast, only 36.4% of spheroids were left using the centrifugation method (Fig. 6c). Media change was either performed using the 3D-tips or

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