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Specific Roles of Akt iso Forms in Apoptosis and Axon Growth Regulation in Neurons
Akt is a member of the AGC kinase family and consists of three isoforms. As one of the major regulators of the class I PI3 kinase pathway, it has a key role in the control of cell metabolism, growth, and survival. Although it has been extensively studied in the nervous system, we have only a faint k...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3324480/ https://www.ncbi.nlm.nih.gov/pubmed/22509246 http://dx.doi.org/10.1371/journal.pone.0032715 |
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author | Diez, Hector Garrido, Juan Jose Wandosell, Francisco |
author_facet | Diez, Hector Garrido, Juan Jose Wandosell, Francisco |
author_sort | Diez, Hector |
collection | PubMed |
description | Akt is a member of the AGC kinase family and consists of three isoforms. As one of the major regulators of the class I PI3 kinase pathway, it has a key role in the control of cell metabolism, growth, and survival. Although it has been extensively studied in the nervous system, we have only a faint knowledge of the specific role of each isoform in differentiated neurons. Here, we have used both cortical and hippocampal neuronal cultures to analyse their function. We characterized the expression and function of Akt isoforms, and some of their substrates along different stages of neuronal development using a specific shRNA approach to elucidate the involvement of each isoform in neuron viability, axon development, and cell signalling. Our results suggest that three Akt isoforms show substantial compensation in many processes. However, the disruption of Akt2 and Akt3 significantly reduced neuron viability and axon length. These changes correlated with a tendency to increase in active caspase 3 and a decrease in the phosphorylation of some elements of the mTORC1 pathway. Indeed, the decrease of Akt2 and more evident the inhibition of Akt3 reduced the expression and phosphorylation of S6. All these data indicate that Akt2 and Akt3 specifically regulate some aspects of apoptosis and cell growth in cultured neurons and may contribute to the understanding of mechanisms of neuron death and pathologies that show deregulated growth. |
format | Online Article Text |
id | pubmed-3324480 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-33244802012-04-16 Specific Roles of Akt iso Forms in Apoptosis and Axon Growth Regulation in Neurons Diez, Hector Garrido, Juan Jose Wandosell, Francisco PLoS One Research Article Akt is a member of the AGC kinase family and consists of three isoforms. As one of the major regulators of the class I PI3 kinase pathway, it has a key role in the control of cell metabolism, growth, and survival. Although it has been extensively studied in the nervous system, we have only a faint knowledge of the specific role of each isoform in differentiated neurons. Here, we have used both cortical and hippocampal neuronal cultures to analyse their function. We characterized the expression and function of Akt isoforms, and some of their substrates along different stages of neuronal development using a specific shRNA approach to elucidate the involvement of each isoform in neuron viability, axon development, and cell signalling. Our results suggest that three Akt isoforms show substantial compensation in many processes. However, the disruption of Akt2 and Akt3 significantly reduced neuron viability and axon length. These changes correlated with a tendency to increase in active caspase 3 and a decrease in the phosphorylation of some elements of the mTORC1 pathway. Indeed, the decrease of Akt2 and more evident the inhibition of Akt3 reduced the expression and phosphorylation of S6. All these data indicate that Akt2 and Akt3 specifically regulate some aspects of apoptosis and cell growth in cultured neurons and may contribute to the understanding of mechanisms of neuron death and pathologies that show deregulated growth. Public Library of Science 2012-04-11 /pmc/articles/PMC3324480/ /pubmed/22509246 http://dx.doi.org/10.1371/journal.pone.0032715 Text en Diez et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Diez, Hector Garrido, Juan Jose Wandosell, Francisco Specific Roles of Akt iso Forms in Apoptosis and Axon Growth Regulation in Neurons |
title | Specific Roles of Akt iso Forms in Apoptosis and Axon Growth Regulation in Neurons |
title_full | Specific Roles of Akt iso Forms in Apoptosis and Axon Growth Regulation in Neurons |
title_fullStr | Specific Roles of Akt iso Forms in Apoptosis and Axon Growth Regulation in Neurons |
title_full_unstemmed | Specific Roles of Akt iso Forms in Apoptosis and Axon Growth Regulation in Neurons |
title_short | Specific Roles of Akt iso Forms in Apoptosis and Axon Growth Regulation in Neurons |
title_sort | specific roles of akt iso forms in apoptosis and axon growth regulation in neurons |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3324480/ https://www.ncbi.nlm.nih.gov/pubmed/22509246 http://dx.doi.org/10.1371/journal.pone.0032715 |
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