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Cell Stress Chaperones. 2018 Nov;23(6):1205-1217. doi: 10.1007/s12192-018-0926-x. Epub 2018 Jun 27.

Stress-induced antioxidant defense and protein chaperone response in the freeze-tolerant wood frog Rana sylvatica.

Author information

1
Department of Veterinary Biomedical Sciences, Western College of Veterinary Medicine, University of Saskatchewan, 52 Campus Dr., Saskatoon, SK, S7N 5B4, Canada.
2
Institute of Biochemistry and Department of Biology, Carleton University, 1125 Colonel By Drive, Ottawa, ON, K1S 5B6, Canada.
3
BioMEMS Resource Center and Center for Engineering in Medicine, Massachusetts General Hospital and Harvard Medical School, 114 16th Street, Charlestown, MA, 02129, USA.
4
Institute of Biochemistry and Department of Biology, Carleton University, 1125 Colonel By Drive, Ottawa, ON, K1S 5B6, Canada. kenneth_storey@carleton.ca.

Abstract

Freeze tolerance is an adaptive response utilized by the wood frog Rana sylvatica to endure the sub-zero temperatures of winter. Survival of whole body freezing requires wood frogs to trigger cryoprotective mechanisms to deal with potential injuries associated with conversion of 65-70% of total body water into ice, including multiple consequences of ice formation such as cessation of blood flow and cell dehydration caused by water loss into ice masses. To understand how wood frogs defend against these stressors, we measured the expression of proteins known to be involved in the antioxidant defense and protein chaperone stress responses in brain and heart of wood frogs comparing freezing, anoxia, and dehydration stress. Our results showed that most stress proteins were regulated in a tissue- and stress-specific manner. Notably, protein levels of the cytosolic superoxide dismutase (SOD1) were upregulated by 1.37 ± 0.11-fold in frozen brain, whereas the mitochondrial SOD2 isoform rose by 1.38 ± 0.37-fold in the heart during freezing. Catalase protein levels were upregulated by 3.01 ± 0.47-fold in the brain under anoxia stress, but remained unchanged in the heart. Similar context-specific regulatory patterns were also observed for the heat shock protein (Hsp) molecular chaperones. Hsp27 protein was down-regulated in the brain across the three stress conditions, whereas the mitochondrial Hsp60 was upregulated in anoxic brain by 1.73 ± 0.38-fold and by 2.13 ± 0.57-fold in the frozen heart. Overall, our study provides a snapshot of the regulatory expression of stress proteins in wood frogs under harsh environment conditions and shows that they are controlled in a tissue- and stress-specific manner.

KEYWORDS:

Anoxia; Cryoprotection; Dehydration; Metabolic depression; Oxidative stress; Redox

PMID:
29951989
PMCID:
PMC6237678
DOI:
10.1007/s12192-018-0926-x
[Indexed for MEDLINE]
Free PMC Article

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