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Fatty acids increase neuronal hypertrophy of Pten knockdown neurons
Phosphatase and tensin homolog (Pten) catalyzes the reverse reaction of PI3K by dephosphorylating PIP3 to PIP2. This negatively regulates downstream Akt/mTOR/S6 signaling resulting in decreased cellular growth and proliferation. Co-injection of a lentivirus knocking Pten down with a control lentivir...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4006057/ https://www.ncbi.nlm.nih.gov/pubmed/24795563 http://dx.doi.org/10.3389/fnmol.2014.00030 |
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author | Fricano, Catherine J. DeSpenza, Tyrone Frazel, Paul W. Li, Meijie O'Malley, A. James Westbrook, Gary L. Luikart, Bryan W. |
author_facet | Fricano, Catherine J. DeSpenza, Tyrone Frazel, Paul W. Li, Meijie O'Malley, A. James Westbrook, Gary L. Luikart, Bryan W. |
author_sort | Fricano, Catherine J. |
collection | PubMed |
description | Phosphatase and tensin homolog (Pten) catalyzes the reverse reaction of PI3K by dephosphorylating PIP3 to PIP2. This negatively regulates downstream Akt/mTOR/S6 signaling resulting in decreased cellular growth and proliferation. Co-injection of a lentivirus knocking Pten down with a control lentivirus allows us to compare the effects of Pten knockdown between individual neurons within the same animal. We find that knockdown of Pten results in neuronal hypertrophy by 21 days post-injection. This neuronal hypertrophy is correlated with increased p-S6 and p-mTOR in individual neurons. We used this system to test whether an environmental factor that has been implicated in cellular hypertrophy could influence the severity of the Pten knockdown-induced hypertrophy. Implantation of mini-osmotic pumps delivering fatty acids results in increased neuronal hypertrophy and p-S6/p-mTOR staining. These hypertrophic effects were reversed in response to rapamycin treatment. However, we did not observe a similar increase in hypertrophy in response to dietary manipulations of fatty acids. Thus, we conclude that by driving growth signaling with fatty acids and knocking down a critical regulator of growth, Pten, we are able to observe an additive morphological phenotype of increased soma size mediated by the mTOR pathway. |
format | Online Article Text |
id | pubmed-4006057 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-40060572014-05-02 Fatty acids increase neuronal hypertrophy of Pten knockdown neurons Fricano, Catherine J. DeSpenza, Tyrone Frazel, Paul W. Li, Meijie O'Malley, A. James Westbrook, Gary L. Luikart, Bryan W. Front Mol Neurosci Neuroscience Phosphatase and tensin homolog (Pten) catalyzes the reverse reaction of PI3K by dephosphorylating PIP3 to PIP2. This negatively regulates downstream Akt/mTOR/S6 signaling resulting in decreased cellular growth and proliferation. Co-injection of a lentivirus knocking Pten down with a control lentivirus allows us to compare the effects of Pten knockdown between individual neurons within the same animal. We find that knockdown of Pten results in neuronal hypertrophy by 21 days post-injection. This neuronal hypertrophy is correlated with increased p-S6 and p-mTOR in individual neurons. We used this system to test whether an environmental factor that has been implicated in cellular hypertrophy could influence the severity of the Pten knockdown-induced hypertrophy. Implantation of mini-osmotic pumps delivering fatty acids results in increased neuronal hypertrophy and p-S6/p-mTOR staining. These hypertrophic effects were reversed in response to rapamycin treatment. However, we did not observe a similar increase in hypertrophy in response to dietary manipulations of fatty acids. Thus, we conclude that by driving growth signaling with fatty acids and knocking down a critical regulator of growth, Pten, we are able to observe an additive morphological phenotype of increased soma size mediated by the mTOR pathway. Frontiers Media S.A. 2014-04-23 /pmc/articles/PMC4006057/ /pubmed/24795563 http://dx.doi.org/10.3389/fnmol.2014.00030 Text en Copyright © 2014 Fricano, DeSpenza, Frazel, Li, O'Malley, Westbrook and Luikart. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Fricano, Catherine J. DeSpenza, Tyrone Frazel, Paul W. Li, Meijie O'Malley, A. James Westbrook, Gary L. Luikart, Bryan W. Fatty acids increase neuronal hypertrophy of Pten knockdown neurons |
title | Fatty acids increase neuronal hypertrophy of Pten knockdown neurons |
title_full | Fatty acids increase neuronal hypertrophy of Pten knockdown neurons |
title_fullStr | Fatty acids increase neuronal hypertrophy of Pten knockdown neurons |
title_full_unstemmed | Fatty acids increase neuronal hypertrophy of Pten knockdown neurons |
title_short | Fatty acids increase neuronal hypertrophy of Pten knockdown neurons |
title_sort | fatty acids increase neuronal hypertrophy of pten knockdown neurons |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4006057/ https://www.ncbi.nlm.nih.gov/pubmed/24795563 http://dx.doi.org/10.3389/fnmol.2014.00030 |
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