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Article: Strategies of biochemical adaptation for hibernation in a South American marsupial, Dromiciops gliroides: 2. Control of the Akt pathway and protein translation machinery

TitleStrategies of biochemical adaptation for hibernation in a South American marsupial, Dromiciops gliroides: 2. Control of the Akt pathway and protein translation machinery
Authors
KeywordsHibernation
Torpor regulation
Monito del monte
Liver
Kidney
Eukaryotic translation initiation factors
Control of protein synthesis
Brain
Issue Date2017
Citation
Comparative Biochemistry and Physiology Part - B: Biochemistry and Molecular Biology, 2017 How to Cite?
Abstract© 2017 Elsevier Inc. When faced with harsh environmental conditions, the South American marsupial, monito del monte (Dromiciops gliroides), reduces its body temperature and uses either daily torpor or multiday hibernation to survive. This study used ELISA and multiplex assays to characterize the responses to hibernation by three regulatory components of protein translation machinery [p-eIF2α(S51), p-eIF4E(S209), p-4EBP(Thr37/46)] and eight targets involved in upstream signaling control of translation [p-IGF-1R(Tyr1135/1136), PTEN(S380), p-Akt(S473), p-GSK-3α(S21), p-GSK-3β(S9), p-TSC2(S939), p-mTOR(S2448), and p70S6K(T412)] . Liver, brain and kidney were analyzed comparing control and hibernation (4. days continuous torpor) conditions. In the liver, increased phosphorylation of IGF-1R, Akt, GSK-3β, TSC2, mTOR, eIF2α, and 4EBP (1.60-1.98 fold compared to control) occurred during torpor suggesting that the regulatory phosphorylation cascade and protein synthesis remained active during torpor. However, responses by brain and kidney differed; torpor resulted in increased phosphorylation of GSK-3β (2.15-4.17 fold) and TSC2 (2.03-3.65 fold), but phosphorylated Akt decreased (to 34-62% of control levels). Torpor also led to an increase in phosphorylated eIF2α (1.4 fold) content in the brain. These patterns of differential protein phosphorylation in brain and kidney were indicative of suppression of protein translation but also could suggest an increase in antioxidant and anti-apoptotic signaling during torpor. Previous studies of liver metabolism in hibernating eutherian mammals have shown that Akt kinase and its downstream signaling components play roles in facilitating hypometabolism by suppressing energy expensive anabolic processes during torpor. However, the results in this study reveal differences between eutherian and marsupial hibernators, suggesting alternative actions of liver Akt during torpor.
Persistent Identifierhttp://hdl.handle.net/10722/253134
ISSN
2021 Impact Factor: 2.495
2020 SCImago Journal Rankings: 0.596
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorLuu, Bryan E.-
dc.contributor.authorWijenayake, Sanoji-
dc.contributor.authorZhang, Jing-
dc.contributor.authorTessier, Shannon N.-
dc.contributor.authorQuintero-Galvis, Julian F.-
dc.contributor.authorGaitán-Espitia, Juan Diego-
dc.contributor.authorNespolo, Roberto F.-
dc.contributor.authorStorey, Kenneth B.-
dc.date.accessioned2018-05-11T05:38:42Z-
dc.date.available2018-05-11T05:38:42Z-
dc.date.issued2017-
dc.identifier.citationComparative Biochemistry and Physiology Part - B: Biochemistry and Molecular Biology, 2017-
dc.identifier.issn1096-4959-
dc.identifier.urihttp://hdl.handle.net/10722/253134-
dc.description.abstract© 2017 Elsevier Inc. When faced with harsh environmental conditions, the South American marsupial, monito del monte (Dromiciops gliroides), reduces its body temperature and uses either daily torpor or multiday hibernation to survive. This study used ELISA and multiplex assays to characterize the responses to hibernation by three regulatory components of protein translation machinery [p-eIF2α(S51), p-eIF4E(S209), p-4EBP(Thr37/46)] and eight targets involved in upstream signaling control of translation [p-IGF-1R(Tyr1135/1136), PTEN(S380), p-Akt(S473), p-GSK-3α(S21), p-GSK-3β(S9), p-TSC2(S939), p-mTOR(S2448), and p70S6K(T412)] . Liver, brain and kidney were analyzed comparing control and hibernation (4. days continuous torpor) conditions. In the liver, increased phosphorylation of IGF-1R, Akt, GSK-3β, TSC2, mTOR, eIF2α, and 4EBP (1.60-1.98 fold compared to control) occurred during torpor suggesting that the regulatory phosphorylation cascade and protein synthesis remained active during torpor. However, responses by brain and kidney differed; torpor resulted in increased phosphorylation of GSK-3β (2.15-4.17 fold) and TSC2 (2.03-3.65 fold), but phosphorylated Akt decreased (to 34-62% of control levels). Torpor also led to an increase in phosphorylated eIF2α (1.4 fold) content in the brain. These patterns of differential protein phosphorylation in brain and kidney were indicative of suppression of protein translation but also could suggest an increase in antioxidant and anti-apoptotic signaling during torpor. Previous studies of liver metabolism in hibernating eutherian mammals have shown that Akt kinase and its downstream signaling components play roles in facilitating hypometabolism by suppressing energy expensive anabolic processes during torpor. However, the results in this study reveal differences between eutherian and marsupial hibernators, suggesting alternative actions of liver Akt during torpor.-
dc.languageeng-
dc.relation.ispartofComparative Biochemistry and Physiology Part - B: Biochemistry and Molecular Biology-
dc.subjectHibernation-
dc.subjectTorpor regulation-
dc.subjectMonito del monte-
dc.subjectLiver-
dc.subjectKidney-
dc.subjectEukaryotic translation initiation factors-
dc.subjectControl of protein synthesis-
dc.subjectBrain-
dc.titleStrategies of biochemical adaptation for hibernation in a South American marsupial, Dromiciops gliroides: 2. Control of the Akt pathway and protein translation machinery-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1016/j.cbpb.2017.12.006-
dc.identifier.scopuseid_2-s2.0-85038822849-
dc.identifier.spagenull-
dc.identifier.epagenull-
dc.identifier.eissn1879-1107-
dc.identifier.isiWOS:000440775700003-
dc.identifier.issnl1096-4959-

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