Search

The in vitro oxygen microenvironment profoundly affects the capacity of cell cultures to model physiological and pathophysiological states. Cell culture is often considered to be hyperoxic, but pericellular oxygen levels, which are affected by oxygen diffusivity and consumption, are rarely reported. Here, we provide evidence that several cell types in culture actually experience local hypoxia, with important implications for cell metabolism and function. We focused initially on adipocytes, as adipose tissue hypoxia is frequently observed in obesity and precedes diminished adipocyte function. Under standard conditions, cultured adipocytes are highly glycolytic and exhibit a transcriptional profile indicative of physiological hypoxia. Increasing pericellular oxygen diverted glucose flux toward mitochondria, lowered HIF1α activity, and resulted in widespread transcriptional rewiring. Functionally, adipocytes increased adipokine secretion and sensitivity to insulin and lipolytic stimuli, recapitulating a healthier adipocyte model. The functional benefits of increasing pericellular oxygen were also observed in macrophages, hPSC-derived hepatocytes and cardiac organoids. Our findings demonstrate that oxygen is limiting in many terminally-differentiated cell types, and that considering pericellular oxygen improves the quality, reproducibility and translatability of culture models. Synopsis: Cell culture is considered a microenvironment with high oxygen. Here, terminally-differentiated cells are shown to be deprived of pericellular oxygen in standard culture systems. mandating tight control of oxygen provision and consumption conditions to ensure experimental reproducibility and translatability to physiology. Cells of various types cultured in standard medium volumes are hypoxic due to oxygen consumption exceeding diffusion rates. Increasing oxygen supply to cultured cells enhances glucose oxidation and anabolic reactions, and causes widespread transcriptional changes. Increased oxygen supply improves the differentiation and function of differentiated cellular models such as adipocytes, macrophages, hPSC-derived hepatocytes and cardiac organoids. Transcriptional responses to limited oxygen in cultured cells match those driven by hypoxia in vivo. Standard cell culture medium volumes dictate a hypoxic pericellular in vitro microenvironment due to oxygen consumption exceeding diffusion rates. [ABSTRACT FROM AUTHOR]