Multi-tissue profile of NFκB pathway regulation during mammalian hibernation.
Adipose Tissue
/ metabolism
Animals
Brain Stem
/ metabolism
Cerebral Cortex
/ metabolism
Fas-Associated Death Domain Protein
/ genetics
Gene Expression Regulation
/ genetics
Heart
/ physiology
Hibernation
/ genetics
Kidney
/ metabolism
Liver
/ metabolism
Male
NF-KappaB Inhibitor alpha
/ metabolism
NF-kappa B
/ genetics
Oxidative Stress
Phosphorylation
Proto-Oncogene Proteins c-myc
/ genetics
Reactive Oxygen Species
/ metabolism
Receptors, Tumor Necrosis Factor, Type I
/ genetics
Sciuridae
/ genetics
Signal Transduction
/ genetics
Spleen
/ metabolism
Metabolic rate depression
Neuroprotection
Nuclear factor kappa-light-chain-enhancer of activated B cells
Thirteen-lined ground squirrel
Torpor
Journal
Comparative biochemistry and physiology. Part B, Biochemistry & molecular biology
ISSN: 1879-1107
Titre abrégé: Comp Biochem Physiol B Biochem Mol Biol
Pays: England
ID NLM: 9516061
Informations de publication
Date de publication:
Historique:
received:
03
02
2020
revised:
12
05
2020
accepted:
14
05
2020
pubmed:
24
5
2020
medline:
13
1
2021
entrez:
24
5
2020
Statut:
ppublish
Résumé
Hibernators have evolved effective mechanisms to overcome the challenges of torpor-arousal cycling. This study focuses on the antioxidant and inflammatory defenses under the control of the redox-sensitive and inflammatory-centered NFκB transcription factor in the thirteen-lined ground squirrel (Ictidomys tridecemlineatus), a well-established model of mammalian hibernation. While hibernators significantly depress oxygen consumption and overall metabolic rate during torpor, arousal brings with it a rapid increase in respiration that is associated with an influx of reactive oxygen species. As such, hibernators employ a variety of antioxidant defenses to combat oxidative damage. Herein, we used Luminex multiplex technology to examine the expression of key proteins in the NFκB transcriptional network, including NFκB, super-repressor IκBα, upstream activators TNFR1 and FADD, and downstream target c-Myc. Transcription factor DNA-binding ELISAs were also used to measure the relative degree of NFκB binding to DNA during hibernation. Analyses were performed across eight different tissues, cerebral cortex, brainstem, white and brown adipose tissue, heart, liver, kidney, and spleen, during euthermic control and late torpor to highlight tissue-specific NFκB mediated cytoprotective responses against oxidative stress experienced during torpor-arousal. Our findings demonstrated brain-specific NFκB activation during torpor, with elevated levels of upstream activators, inactive-phosphorylated IκBα, active-phosphorylated NFκB, and enhanced NFκB-DNA binding. Protein levels of downstream protein, c-Myc, also increased in the brain and adipose tissues during late torpor. The results show that NFκB regulation might serve a critical neuroprotective and cytoprotective role in hibernating brains and selective peripheral tissue.
Identifiants
pubmed: 32445797
pii: S1096-4959(20)30054-3
doi: 10.1016/j.cbpb.2020.110460
pii:
doi:
Substances chimiques
Fas-Associated Death Domain Protein
0
NF-kappa B
0
Proto-Oncogene Proteins c-myc
0
Reactive Oxygen Species
0
Receptors, Tumor Necrosis Factor, Type I
0
NF-KappaB Inhibitor alpha
139874-52-5
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
110460Informations de copyright
Copyright © 2020 Elsevier Inc. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of Competing Interest Authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.