Abstract

Mammalian cell culture is widely used for discovery and development. Recently, increasing attention has been paid to the importance of maintaining physiologically-relevant conditions in cell culture. Although oxygen level is a particularly important consideration, it is rarely regulated by experimentalists. The atmospheric O2 levels commonly used in cell culture are significantly higher than those experienced by most mammalian cells in vivo, leaving cells susceptible to oxidative damage, senescence, transformation, and otherwise aberrant physiology. A barrier to incorporating O2 regulation into most cell culture workflows has been the expense of investing in new equipment, as the vast majority of laboratory CO2 incubators do not regulate O2. Here, we describe an inexpensive (<CAD 1000), portable and user-friendly O2/CO2 incubator that can establish and maintain physiological O2, CO2, and temperature values within their physiological ranges. We used an Arduino-based approach to add O2 and CO2 control to a temperature-regulating egg incubator. Our incubator was tested against a commercial laboratory O2/CO2 incubator. Using Presens OxoDish technology, we demonstrate that at a setpoint value of 5% gas-phase incubator O2, media O2 averaged 5.03 (SD = 0.03) with a range of 4.98–5.09%. MCF7, LNCaP and C2C12 cell lines cultured in the incubator displayed normal morphology, proliferation, and viability. Culture for up to one week produced no contamination. Thus, our incubator provides an inexpensive means of maintaining physioxia in routine mammalian cell culture.

Highlights

  • There is a growing realization amongst biologists of the importance of maintaining physiologically representative conditions during cell culture [1–6]. This has culminated in the development of physiologic media such as human plasma-like media (HPLM) [1] and Plasmax [4], which are modeled on the human blood plasma metabolome

  • In the absence of O2 regulation in typical cell culture incubators it equilibrates to approximately 18–19%, which is substantially hyperoxic and drives the production of excess reactive oxygen species (ROS) and reactive nitrogen species (RNS) from a variety of cellular sources ([7]; reviewed in [6])

  • Using the Presens OxoDish/SensorDish system, we show that no pericellular hypoxia occurred in sideration when culturing cells in physioxia

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Summary

Introduction

There is a growing realization amongst biologists of the importance of maintaining physiologically representative conditions during cell culture [1–6]. In the absence of O2 regulation in typical cell culture incubators it equilibrates to approximately 18–19%, which is substantially hyperoxic and drives the production of excess reactive oxygen species (ROS) and reactive nitrogen species (RNS) from a variety of cellular sources ([7]; reviewed in [6]). These excess ROS/RNS can induce the pathological oxidation of proteins, lipids and nucleic acids, causing the disruption of a variety of biological processes and signal transduction pathways [8–10]

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