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- Publisher Website: 10.1016/j.cbpb.2017.12.007
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Article: Strategies of biochemical adaptation for hibernation in a South American marsupial Dromiciops gliroides: 1. Mitogen-activated protein kinases and the cell stress response
Title | Strategies of biochemical adaptation for hibernation in a South American marsupial Dromiciops gliroides: 1. Mitogen-activated protein kinases and the cell stress response |
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Authors | |
Keywords | MAPK signal transduction cascades Monito del monte Metabolic rate depression South American marsupial Transcription factor regulation |
Issue Date | 2017 |
Citation | Comparative Biochemistry and Physiology Part - B: Biochemistry and Molecular Biology, 2017 How to Cite? |
Abstract | © 2017 Elsevier Inc. Hibernation is a period of torpor and heterothermy that is typically associated with a strong reduction in metabolic rate, global suppression of transcription and translation, and upregulation of various genes/proteins that are central to the cellular stress response such as protein kinases, antioxidants, and heat shock proteins. The current study examined cell signaling cascades in hibernating monito del monte, Dromiciops gliroides, a South American marsupial of the Order Microbiotheria. Responses to hibernation by members of the mitogen-activated protein kinase (MAPK) pathways, and their roles in coordinating hibernator metabolism were examined in liver, kidney, heart and brain of control and versus hibernating (4. days continuous torpor) D. gliroides. The targets evaluated included key protein kinases in their activated phosphorylated forms (p-ERK/MAPK 1/2, p-MEK1, p-MSK1, p-p38, p-JNK) and related target proteins (p-CREB 2, p-ATF2, p-c-Jun and p-p53). Liver exhibited a strong coordinated response by MAPK members to hibernation with significant increases in protein phosphorylation levels of p-MEK1, p-ERK/MAPK1/2, p-MSK1, p-JNK and target proteins c-Jun, and p-ATF2, all combining to signify a strong activation of MAPK signaling during hibernation. Kidney also showed activation of MAPK cascades with significant increases in p-MEK1, p-ERK/MAPK1/2, p-p38, and p-c-Jun levels in hibernating animals. By contrast, responses by heart and brain indicated reduced MAPK pathway function during torpor with reduced phosphorylation of targets including p-ERK/MAPK 1/2 in both tissues as well as lower p-p38 and p-JNK content in heart. Overall, the data indicate a vital role for MAPK signaling in regulating the cell stress response during marsupial hibernation. |
Persistent Identifier | http://hdl.handle.net/10722/253183 |
ISSN | 2023 Impact Factor: 1.9 2023 SCImago Journal Rankings: 0.518 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Wijenayake, Sanoji | - |
dc.contributor.author | Luu, Bryan E. | - |
dc.contributor.author | Zhang, Jing | - |
dc.contributor.author | Tessier, Shannon N. | - |
dc.contributor.author | Quintero-Galvis, Julian F. | - |
dc.contributor.author | Gaitán-Espitia, Juan Diego | - |
dc.contributor.author | Nespolo, Roberto F. | - |
dc.contributor.author | Storey, Kenneth B. | - |
dc.date.accessioned | 2018-05-11T05:38:50Z | - |
dc.date.available | 2018-05-11T05:38:50Z | - |
dc.date.issued | 2017 | - |
dc.identifier.citation | Comparative Biochemistry and Physiology Part - B: Biochemistry and Molecular Biology, 2017 | - |
dc.identifier.issn | 1096-4959 | - |
dc.identifier.uri | http://hdl.handle.net/10722/253183 | - |
dc.description.abstract | © 2017 Elsevier Inc. Hibernation is a period of torpor and heterothermy that is typically associated with a strong reduction in metabolic rate, global suppression of transcription and translation, and upregulation of various genes/proteins that are central to the cellular stress response such as protein kinases, antioxidants, and heat shock proteins. The current study examined cell signaling cascades in hibernating monito del monte, Dromiciops gliroides, a South American marsupial of the Order Microbiotheria. Responses to hibernation by members of the mitogen-activated protein kinase (MAPK) pathways, and their roles in coordinating hibernator metabolism were examined in liver, kidney, heart and brain of control and versus hibernating (4. days continuous torpor) D. gliroides. The targets evaluated included key protein kinases in their activated phosphorylated forms (p-ERK/MAPK 1/2, p-MEK1, p-MSK1, p-p38, p-JNK) and related target proteins (p-CREB 2, p-ATF2, p-c-Jun and p-p53). Liver exhibited a strong coordinated response by MAPK members to hibernation with significant increases in protein phosphorylation levels of p-MEK1, p-ERK/MAPK1/2, p-MSK1, p-JNK and target proteins c-Jun, and p-ATF2, all combining to signify a strong activation of MAPK signaling during hibernation. Kidney also showed activation of MAPK cascades with significant increases in p-MEK1, p-ERK/MAPK1/2, p-p38, and p-c-Jun levels in hibernating animals. By contrast, responses by heart and brain indicated reduced MAPK pathway function during torpor with reduced phosphorylation of targets including p-ERK/MAPK 1/2 in both tissues as well as lower p-p38 and p-JNK content in heart. Overall, the data indicate a vital role for MAPK signaling in regulating the cell stress response during marsupial hibernation. | - |
dc.language | eng | - |
dc.relation.ispartof | Comparative Biochemistry and Physiology Part - B: Biochemistry and Molecular Biology | - |
dc.subject | MAPK signal transduction cascades | - |
dc.subject | Monito del monte | - |
dc.subject | Metabolic rate depression | - |
dc.subject | South American marsupial | - |
dc.subject | Transcription factor regulation | - |
dc.title | Strategies of biochemical adaptation for hibernation in a South American marsupial Dromiciops gliroides: 1. Mitogen-activated protein kinases and the cell stress response | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1016/j.cbpb.2017.12.007 | - |
dc.identifier.scopus | eid_2-s2.0-85038884078 | - |
dc.identifier.spage | null | - |
dc.identifier.epage | null | - |
dc.identifier.eissn | 1879-1107 | - |
dc.identifier.isi | WOS:000440775700002 | - |
dc.identifier.issnl | 1096-4959 | - |