Mitochondria and the Frozen Frog.
Janet M StoreyShaobo WuKenneth B StoreyPublished in: Antioxidants (Basel, Switzerland) (2021)
The wood frog, Rana sylvatica, is the best-studied of a small group of amphibian species that survive whole body freezing during the winter months. These frogs endure the freezing of 65-70% of their total body water in extracellular ice masses. They have implemented multiple adaptations that manage ice formation, deal with freeze-induced ischemia/reperfusion stress, limit cell volume reduction with the production of small molecule cryoprotectants (glucose, urea) and adjust a wide variety of metabolic pathways for prolonged life in a frozen state. All organs, tissues, cells and intracellular organelles are affected by freeze/thaw and its consequences. This article explores mitochondria in the frozen frog with a focus on both the consequences of freezing (e.g., anoxia/ischemia, cell volume reduction) and mitigating defenses (e.g., antioxidants, chaperone proteins, upregulation of mitochondria-encoded genes, enzyme regulation, etc.) in order to identify adaptive strategies that defend and adapt mitochondria in animals that can be frozen for six months or more every year. A particular focus is placed on freeze-responsive genes in wood frogs that are encoded on the mitochondrial genome including ATP6/8, ND4 and 16S RNA. These were strongly up-regulated during whole body freezing (24 h at -2.5 °C) in the liver and brain but showed opposing responses to two component stresses: strong upregulation in response to anoxia but no response to dehydration stress. This indicates that freeze-responsive upregulation of mitochondria-encoded genes is triggered by declining oxygen and likely has an adaptive function in supporting cellular energetics under indeterminate lengths of whole body freezing.
Keyphrases
- endoplasmic reticulum
- reactive oxygen species
- cell death
- genome wide
- small molecule
- poor prognosis
- cell proliferation
- single cell
- cell cycle arrest
- cell therapy
- signaling pathway
- genome wide identification
- induced apoptosis
- bioinformatics analysis
- cancer therapy
- oxidative stress
- magnetic resonance imaging
- endoplasmic reticulum stress
- endothelial cells
- blood glucose
- long non coding rna
- drug delivery
- brain injury
- diabetic rats
- adipose tissue
- protein protein
- blood pressure
- genome wide analysis
- pi k akt
- subarachnoid hemorrhage
- weight loss