4.7 Article

O2-sensing signal cascade:: clamping of O2 respiration, reduced ATP utilization, and inducible fumarate respiration

Journal

AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY
Volume 295, Issue 1, Pages C29-C37

Publisher

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajpcell.00466.2007

Keywords

mitochondrial membrane potential; hibernation; cardioprotection

Funding

  1. NCRR NIH HHS [C06 RR 015455] Funding Source: Medline
  2. NHLBI NIH HHS [R01 HL 084302] Funding Source: Medline

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These studies explore the consequences of activating the prolyl hydroxylase (PHD) O-2-sensing pathway in spontaneously twitching neonatal cardiomyocytes. Full activation of the PHD pathway was achieved using the broad-spectrum PHD inhibitor (PHI) dimethyloxaloylglycine (DMOG). PHI treatment of cardiomyocytes caused an 85% decrease in O-2 consumption and a 300% increase in lactic acid production under basal conditions. This indicates a similar to 75% decrease in ATP turnover rate, inasmuch as the increased ATP generation by glycolysis is inadequate to compensate for the lower respiration. To determine the extent to which decreased ATP turnover underlies the suppressed O-2 consumption, mitochondria were uncoupled with 2,4-dinitrophenol. We were surprised to find that 2,4-dinitrophenol failed to increase O-2 consumption by PHI-treated cells, indicating that electron transport chain activity, rather than ATP turnover rate, limits respiration in PHI-treated cardiomyocytes. Silencing of hypoxia-inducible factor-1 alpha (HIF-1 alpha) expression restored the ability of uncoupled PHI-treated myocytes to increase O-2 consumption; however, basal O-2 uptake rates remained low because of the unabated suppression of cellular ATP consumption. Thus it appears that respiration is actively clamped through an HIF-dependent mechanism, whereas HIF-independent mechanisms are responsible for downregulation of ATP consumption. In addition, we find that PHD pathway activation enables mitochondria to utilize fumarate as a terminal electron acceptor when cytochrome c oxidase is inactive. The source of fumarate for this unusual respiration is derived from aspartate via the purine nucleotide cycle. In sum, these studies show that the O-2-sensing pathway is sufficient to actively clamp O-2 consumption and independently suppress cellular ATP consumption. The PHD pathway also enables the mitochondria to utilize fumarate for respiration.

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