Modulation of the Akt Pathway Reveals a Novel Link with PERK/eIF2α, which Is Relevant during Hypoxia
The unfolded protein response (UPR) and the Akt signaling pathway share several regulatory functions and have the capacity to determine cell outcome under specific conditions. However, both pathways have largely been studied independently. Here, we asked whether the Akt pathway regulates the UPR. To...
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Acceso en línea: | http://hdl.handle.net/20.500.12110/paper_19326203_v8_n7_p_Blaustein |
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paperaa:paper_19326203_v8_n7_p_Blaustein2023-06-12T16:51:48Z Modulation of the Akt Pathway Reveals a Novel Link with PERK/eIF2α, which Is Relevant during Hypoxia PLoS ONE 2013;8(7) Blaustein, M. Pérez-Munizaga, D. Sánchez, M.A. Urrutia, C. Grande, A. Risso, G. Srebrow, A. Alfaro, J. Colman-Lerner, A. activating transcription factor 6 cell protein initiation factor 2alpha inositol requiring protein 1 PERK protein phosphatidylinositol 3 kinase protein kinase B unclassified drug article cell death cell fate controlled study human human cell hypoxia physiological process protein phosphorylation protein protein interaction protein targeting protein unfolding signal transduction Cell Hypoxia Cell Line Cell Line, Tumor Cell Survival eIF-2 Kinase Eukaryotic Initiation Factor-2 HeLa Cells Humans Proto-Oncogene Proteins c-akt The unfolded protein response (UPR) and the Akt signaling pathway share several regulatory functions and have the capacity to determine cell outcome under specific conditions. However, both pathways have largely been studied independently. Here, we asked whether the Akt pathway regulates the UPR. To this end, we used a series of chemical compounds that modulate PI3K/Akt pathway and monitored the activity of the three UPR branches: PERK, IRE1 and ATF6. The antiproliferative and antiviral drug Akt-IV strongly and persistently activated all three branches of the UPR. We present evidence that activation of PERK/eIF2α requires Akt and that PERK is a direct Akt target. Chemical activation of this novel Akt/PERK pathway by Akt-IV leads to cell death, which was largely dependent on the presence of PERK and IRE1. Finally, we show that hypoxia-induced activation of eIF2α requires Akt, providing a physiologically relevant condition for the interaction between Akt and the PERK branch of the UPR. These data suggest the UPR and the Akt pathway signal to one another as a means of controlling cell fate. © 2013 Blaustein et al. Fil:Blaustein, M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Grande, A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Risso, G. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Srebrow, A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Colman-Lerner, A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 2013 info:eu-repo/semantics/article info:ar-repo/semantics/artículo info:eu-repo/semantics/publishedVersion application/pdf eng info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_19326203_v8_n7_p_Blaustein |
institution |
Universidad de Buenos Aires |
institution_str |
I-28 |
repository_str |
R-134 |
collection |
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) |
language |
Inglés |
orig_language_str_mv |
eng |
topic |
activating transcription factor 6 cell protein initiation factor 2alpha inositol requiring protein 1 PERK protein phosphatidylinositol 3 kinase protein kinase B unclassified drug article cell death cell fate controlled study human human cell hypoxia physiological process protein phosphorylation protein protein interaction protein targeting protein unfolding signal transduction Cell Hypoxia Cell Line Cell Line, Tumor Cell Survival eIF-2 Kinase Eukaryotic Initiation Factor-2 HeLa Cells Humans Proto-Oncogene Proteins c-akt |
spellingShingle |
activating transcription factor 6 cell protein initiation factor 2alpha inositol requiring protein 1 PERK protein phosphatidylinositol 3 kinase protein kinase B unclassified drug article cell death cell fate controlled study human human cell hypoxia physiological process protein phosphorylation protein protein interaction protein targeting protein unfolding signal transduction Cell Hypoxia Cell Line Cell Line, Tumor Cell Survival eIF-2 Kinase Eukaryotic Initiation Factor-2 HeLa Cells Humans Proto-Oncogene Proteins c-akt Blaustein, M. Pérez-Munizaga, D. Sánchez, M.A. Urrutia, C. Grande, A. Risso, G. Srebrow, A. Alfaro, J. Colman-Lerner, A. Modulation of the Akt Pathway Reveals a Novel Link with PERK/eIF2α, which Is Relevant during Hypoxia |
topic_facet |
activating transcription factor 6 cell protein initiation factor 2alpha inositol requiring protein 1 PERK protein phosphatidylinositol 3 kinase protein kinase B unclassified drug article cell death cell fate controlled study human human cell hypoxia physiological process protein phosphorylation protein protein interaction protein targeting protein unfolding signal transduction Cell Hypoxia Cell Line Cell Line, Tumor Cell Survival eIF-2 Kinase Eukaryotic Initiation Factor-2 HeLa Cells Humans Proto-Oncogene Proteins c-akt |
description |
The unfolded protein response (UPR) and the Akt signaling pathway share several regulatory functions and have the capacity to determine cell outcome under specific conditions. However, both pathways have largely been studied independently. Here, we asked whether the Akt pathway regulates the UPR. To this end, we used a series of chemical compounds that modulate PI3K/Akt pathway and monitored the activity of the three UPR branches: PERK, IRE1 and ATF6. The antiproliferative and antiviral drug Akt-IV strongly and persistently activated all three branches of the UPR. We present evidence that activation of PERK/eIF2α requires Akt and that PERK is a direct Akt target. Chemical activation of this novel Akt/PERK pathway by Akt-IV leads to cell death, which was largely dependent on the presence of PERK and IRE1. Finally, we show that hypoxia-induced activation of eIF2α requires Akt, providing a physiologically relevant condition for the interaction between Akt and the PERK branch of the UPR. These data suggest the UPR and the Akt pathway signal to one another as a means of controlling cell fate. © 2013 Blaustein et al. |
format |
Artículo Artículo publishedVersion |
author |
Blaustein, M. Pérez-Munizaga, D. Sánchez, M.A. Urrutia, C. Grande, A. Risso, G. Srebrow, A. Alfaro, J. Colman-Lerner, A. |
author_facet |
Blaustein, M. Pérez-Munizaga, D. Sánchez, M.A. Urrutia, C. Grande, A. Risso, G. Srebrow, A. Alfaro, J. Colman-Lerner, A. |
author_sort |
Blaustein, M. |
title |
Modulation of the Akt Pathway Reveals a Novel Link with PERK/eIF2α, which Is Relevant during Hypoxia |
title_short |
Modulation of the Akt Pathway Reveals a Novel Link with PERK/eIF2α, which Is Relevant during Hypoxia |
title_full |
Modulation of the Akt Pathway Reveals a Novel Link with PERK/eIF2α, which Is Relevant during Hypoxia |
title_fullStr |
Modulation of the Akt Pathway Reveals a Novel Link with PERK/eIF2α, which Is Relevant during Hypoxia |
title_full_unstemmed |
Modulation of the Akt Pathway Reveals a Novel Link with PERK/eIF2α, which Is Relevant during Hypoxia |
title_sort |
modulation of the akt pathway reveals a novel link with perk/eif2α, which is relevant during hypoxia |
publishDate |
2013 |
url |
http://hdl.handle.net/20.500.12110/paper_19326203_v8_n7_p_Blaustein |
work_keys_str_mv |
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1769810355916111872 |