Abstract

The mitochondrion is one of the key organelles for maintaining cellular homeostasis. External environmental stimuli and internal regulatory processes may alter the metabolism and functions of mitochondria. To understand these activities of mitochondria, it is critical to probe the key metabolic molecules inside these organelles. In this study, we used label-free chemical imaging modalities including coherent anti-Stokes Raman scattering and multiphoton-excited fluorescence to investigate the mitochondrial activities in living cancer cells. We found that hypothermia exposure tends to induce fatty-acid (FA) accumulation in some mitochondria of MIAPaCa-2 cells. Autofluorescence images show that the FA-accumulated mitochondria also have abnormal metabolism of nicotinamide adenine dinucleotide hydrogen, likely induced by the dysfunction of the electron transport chain. We also found that when the cells were re-warmed to physiological temperature after a period of hypothermia, the FA-accumulated mitochondria changed their structural features. To the best of our knowledge, this is the first time that FA accumulation in mitochondria was observed in live cells. Our research also demonstrates that multimodal label-free chemical imaging is an attractive tool to discover abnormal functions of mitochondria at the single-organelle level and can be used to quantify the dynamic changes of these organelles under perturbative conditions.

Highlights

  • The mitochondrion is one of the key organelles for maintaining cellular homeostasis

  • coherent anti-Stokes Raman scattering (CARS) signals were acquired in the forward direction using a photo-multiplier tube (PMT, Hamamatsu H7422P), while multiphoton excitation fluorescence (MPEF) signals were collected in the epi direction using separate PMTs

  • If we take the intensity ratio of nicotinamide adenine dinucleotide hydrogen (NADH)/(NADH + flavin adenine dinucleotide (FAD)), which is defined as the redox ratio, we find that these fatty acids (FAs)-accumulated mitochondria tend to have a higher value than other parts of the cell

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Summary

Introduction

The mitochondrion is one of the key organelles for maintaining cellular homeostasis. External environmental stimuli and internal regulatory processes may alter the metabolism and functions of mitochondria. We used label-free chemical imaging modalities including coherent anti-Stokes Raman scattering and multiphoton-excited fluorescence to investigate the mitochondrial activities in living cancer cells. Our research demonstrates that multimodal label-free chemical imaging is an attractive tool to discover abnormal functions of mitochondria at the single-organelle level and can be used to quantify the dynamic changes of these organelles under perturbative conditions. Using time-lapse CARS imaging, we followed individual mitochondria trafficking and found that these dysfunctional organelles changed structures after the cells were warmed back to the physiological temperature. This research highlights label-free multimodal chemical imaging as a unique tool to visualize the changes in chemical composition and function of mitochondria at the single-organelle level. Future studies will continue to unveil the dynamic formation of stressed mitochondria under various conditions

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