Abstract

Oxidative stress and reactive oxygen species (ROS) are central to many physiological and pathophysiological processes. However, due to multiple technical challenges, it is hard to capture a comprehensive readout of the cell, involving both biochemical and functional status. We addressed this problem by developing a fully parallelized workflow for metabolomics (providing absolute quantities for > 100 metabolites including TCA cycle, pentose phosphate pathway, purine metabolism, glutathione metabolism, cysteine and methionine metabolism, glycolysis and gluconeogenesis) and live cell imaging microscopy. The correlative imaging strategy was applied to study morphological and metabolic adaptation of cancer cells upon short-term hydrogen peroxide (H2O2) exposure in vitro. The combination provided rich metabolic information at the endpoint of exposure together with imaging of mitochondrial effects. As a response, superoxide concentrations were elevated with a strong mitochondrial localization, and multi-parametric image analysis revealed a shift towards fragmentation. In line with this, metabolism reflected both the impaired mitochondrial function and shifts to support the first-line cellular defense and compensate for energy loss. The presented workflow combining high-end technologies demonstrates the applicability for the study of short-term oxidative stress, but it can be suitable for the in-depth study of various short-term oxidative and other cellular stress-related phenomena.

Highlights

  • Oxidative stress and reactive oxygen species (ROS) are central to many physiological and pathophysiological processes

  • The correlative metabolomics/imaging method comprised parallel in vitro experiments followed by tailored sample preparation for metabolomics and staining for microscopy

  • In a proof-of-principle experiment, HCT116 colon cancer cells were exposed to hydrogen peroxide for a short period (2h) in live cell imaging medium and this perturbation could be investigated on both morphological and molecular levels

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Summary

Introduction

Oxidative stress and reactive oxygen species (ROS) are central to many physiological and pathophysiological processes. Due to multiple technical challenges, it is hard to capture a comprehensive readout of the cell, involving both biochemical and functional status We addressed this problem by developing a fully parallelized workflow for metabolomics (providing absolute quantities for > 100 metabolites including TCA cycle, pentose phosphate pathway, purine metabolism, glutathione metabolism, cysteine and methionine metabolism, glycolysis and gluconeogenesis) and live cell imaging microscopy. Under physiological conditions the bulk of ROS originate from the mitochondria, as side products of aerobic respiration, representing a possible source of internal stress All these aspects make the study of redox stress in a mitochondrial context relevant, both in a functional, spatial and mechanistic perspective. The described method enabled rapid mitochondrial isolation by an epitope-tagged mitochondrial membrane protein

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