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. 2025 Sep 24.
doi: 10.1113/JP288755. Online ahead of print.

Hypoxia exposure fine-tunes mitochondrial function in sea turtle cells

B Gabriela Arango  1 , David C Ensminger  2 , Dianna Xing  1 , Céline A Godard-Codding  3 , José Pablo Vázquez-Medina  1
Affiliations

Hypoxia exposure fine-tunes mitochondrial function in sea turtle cells

B Gabriela Arango et al. J Physiol. .

Abstract

Sea turtles experience extreme fluctuations in oxygen levels derived from extended breath-hold diving, yet the cellular adjustments underlying hypoxia tolerance in these animals remain poorly understood. Here, we employed metabolite profiling, extracellular flux assays and microscopy analyses of the mitochondrial reticulum to investigate how primary cells derived from sea turtles and lizards cope with extended hypoxia exposure. Cells from both species proliferate in primary culture, stain positive for fibroblast markers, are metabolically active and stabilize HIF1-α when exposed to chemical or environmental hypoxia. In contrast to lizard cells, sea turtle cells exhibit a faster and more robust response to 1 h or 24 h of hypoxia exposure (0.1% O2), upregulating antioxidant pathways and optimizing oxygen use rather than relying on glycolytic metabolism. Similarly, mitochondrial reticulum architecture is maintained without apparent fragmentation during hypoxia exposure in sea turtle cells. Consistent with these observations, sea turtle mitochondria maintain better function during reoxygenation following 24 h of hypoxia exposure. These findings show that sea turtle cells undergo intrinsic metabolic adjustments to cope with extreme oxygen fluctuations, aligning with the remarkable hypoxic tolerance exhibited by these animals, which can endure up to 7 h of breath-holding underwater. KEY POINTS: Hypoxic sea turtle cells bypass the Crabtree effect and boost antioxidant defences. Hypoxia exposure fine-tunes mitochondrial function in sea turtle cells. Preserving mitochondrial architecture during hypoxia may help sea turtle cells restart respiration upon reoxygenation after extended hypoxia.

Keywords: cellular respiration; diving; metabolomics; oxidative stress; reptiles.

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