Citric acid cycle

Organic chemistry

Enzyme

Mitochondrial DNA

Dehydrogenase

NADH dehydrogenase

Biology

Gene

Malate dehydrogenase

Electron transport chain

Chemistry

Respiratory chain

Mitochondrial respiratory chain

Oxidative phosphorylation

NAD+ kinase

Succinate dehydrogenase

Mitochondrion

Cytosol

Biochemistry

Redox

Biochimica et Biophysica Acta (BBA) - Bioenergetics

The mitochondrial respiratory chain (RC) enables many metabolic processes by regenerating both mitochondrial and cytosolic NAD+ and ATP. The oxidation by the RC of the NADH metabolically produced in the cytosol involves redox shuttles as the malate-aspartate shuttle (MAS) and is of paramount importance for cell fate. However, the specific metabolic regulations allowing mitochondrial respiration to prioritize NADH oxidation in response to high NADH/NAD+ redox stress have not been elucidated. The recent discovery that complex I (NADH dehydrogenase), and not complex II (Succinate dehydrogenase), can assemble with other respiratory chain complexes to form functional entities called respirasomes, led to the assumption that this supramolecular organization would favour NADH oxidation. Unexpectedly, characterization of heart and liver mitochondria demonstrates that the RC systematically favours electrons provided by the 'respirasome free' complex II. Our results demonstrate that the preferential succinate driven respiration is tightly controlled by OAA levels, and that OAA feedback inhibition of complex II rewires RC fuelling increasing NADH oxidation capacity. This new regulatory mechanism synergistically increases RC's NADH oxidative capacity and rewires MDH2 driven anaplerosis of the TCA, preventing malate production from succinate to favour oxidation of cytosolic malate. This regulatory mechanism synergistically adjusts RC and TCA fuelling in response to extramitochondrial malate produced by the MAS.

MDH2 produced OAA is a metabolic switch rewiring the fuelling of respiratory chain and TCA cycle