Monitoring live mitochondrial metabolism in real‐time using NMR spectroscopy

Author:

Nagana Gowda G. A.12ORCID,Pascua Vadim12,Lusk John A.12,Hong Natalie N.12,Guo Lin1,Dong Jiyang13ORCID,Sweet Ian R.4,Raftery Daniel125ORCID

Affiliation:

1. Northwest Metabolomics Research Center, Anesthesiology and Pain Medicine University of Washington Seattle Washington USA

2. Mitochondria and Metabolism Center, Anesthesiology and Pain Medicine University of Washington Seattle Washington USA

3. Department of Electronic Science Xiamen University Xiamen China

4. Department of Medicine University of Washington Seattle Washington USA

5. Fred Hutchinson Cancer Center Seattle Washington USA

Abstract

AbstractInvestigation of mitochondrial metabolism is gaining increased interest owing to the growing recognition of the role of mitochondria in health and numerous diseases. Studies of isolated mitochondria promise novel insights into the metabolism devoid of confounding effects from other cellular organelles such as cytoplasm. This study describes the isolation of mitochondria from mouse skeletal myoblast cells (C2C12) and the investigation of live mitochondrial metabolism in real‐time using isotope tracer‐based NMR spectroscopy. [3‐13C1]pyruvate was used as the substrate to monitor the dynamic changes of the downstream metabolites in mitochondria. The results demonstrate an intriguing phenomenon, in which lactate is produced from pyruvate inside the mitochondria and the results were confirmed by treating mitochondria with an inhibitor of mitochondrial pyruvate carrier (UK5099). Lactate is associated with health and numerous diseases including cancer and, to date, it is known to occur only in the cytoplasm. The insight that lactate is also produced inside mitochondria opens avenues for exploring new pathways of lactate metabolism. Further, experiments performed using inhibitors of the mitochondrial respiratory chain, FCCP and rotenone, show that [2‐13C1]acetyl coenzyme A, which is produced from [3‐13C1]pyruvate and acts as a primary substrate for the tricarboxylic acid cycle in mitochondria, exhibits a remarkable sensitivity to the inhibitors. These results offer a direct approach to visualize mitochondrial respiration through altered levels of the associated metabolites.

Funder

National Center for Advancing Translational Sciences

National Institute of Diabetes and Digestive and Kidney Diseases

Publisher

Wiley

Subject

General Materials Science,General Chemistry

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