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. 2019 Feb;71(1):443-452.
doi: 10.1007/s10616-018-0263-z. Epub 2018 Dec 4.

Proliferation characteristics of cells cultured under periodic versus static conditions

Affiliations

Proliferation characteristics of cells cultured under periodic versus static conditions

Daniel F Gilbert et al. Cytotechnology. 2019 Feb.

Abstract

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 HEK293YFPI152L cells, stably expressing yellow fluorescent protein. Cells were grown for ~ 30 h at 37 °C and ambient CO2 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.

Keywords: Biochip; Cell growth; HEK293; Long-term time-lapse microscopy; Microfluidics; YFPI152L.

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Conflict of interest statement

JW is CEO and shareholder of Cellasys GmbH.

Figures

Fig. 1
Fig. 1
Setup and workflow for long-term culture and parallel time-lapse imaging. a 3D printed chip carrier. The carrier was printed using the biocompatible thermoplast ABS and has the dimensions of a standard multi-titer plate. It provides wells for two biochips and a standard 6 cm cell culture dish (see ‘h’ in b). During life-cell imaging the culture dish is filled with 4 ml water, serving as a reference for the thermistor (see ‘k’ in b) and the environment control infrastructure of the microscope. Cells are imaged through a pinhole at the bottom of the carrier. b Setup for establishing static and periodic culturing conditions during time-lapse long-term imaging. (a) medium waste bottle, (b) peristaltic pump, (c) medium reservoir bottle, (d) waste tubing, (e) perfusion tubing, (f) imaging chamber, (g) 3D printed chip carrier, (h) water reservoir for thermistor, (i) chip for perfusion culture, (j) chip for static culture, (k) thermistor cable and connector. c Experimental workflow for comparative cell growth analysis. Details see text
Fig. 2
Fig. 2
Comparative analysis of cellular growth characteristics of HEK293YFPI152L cells at static versus periodic culturing conditions. a Representative fluomicrographs of HEK293YFPI152L cells cultured in multi-parametric cell chips in static (upper row) and periodic (bottom row) culture mode at experiment initiation (start) and after 30 h imaging duration (end). Scale bar: 200 µm. b Time courses of the average confluence (in %, mean ± SD, N = 4) of cells cultured in static (black) and periodic (red) culture mode, respectively, calculated from images as shown in (a). The time courses indicate exponential and linear growth for cells cultured in static and periodic mode, respectively. The inset histogram displays the average fold-change in growth area (mean ± SD, N = 4) and indicates that the final growth area is comparable for both culture conditions after 30 h culture duration. ‘n.s.’: not significant. (Color figure online)

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