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AKT and its related molecular feature in aged mice skin
Previous studies suggest that Akt signaling promotes tissue regeneration and decreased Akt activities are found in aged tissues. However, this study finds that the expression and activation levels of Akt in the mice skin increased with age. Additionally, the expression levels of Pten, p16, p21 and p...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5462418/ https://www.ncbi.nlm.nih.gov/pubmed/28591208 http://dx.doi.org/10.1371/journal.pone.0178969 |
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author | Chen, Haiyan Wang, Xusheng Han, Jimin Fan, Zhimeng Sadia, Sobia Zhang, Rongrong Guo, Yingsheng Jiang, Yuyang Wu, Yaojiong |
author_facet | Chen, Haiyan Wang, Xusheng Han, Jimin Fan, Zhimeng Sadia, Sobia Zhang, Rongrong Guo, Yingsheng Jiang, Yuyang Wu, Yaojiong |
author_sort | Chen, Haiyan |
collection | PubMed |
description | Previous studies suggest that Akt signaling promotes tissue regeneration and decreased Akt activities are found in aged tissues. However, this study finds that the expression and activation levels of Akt in the mice skin increased with age. Additionally, the expression levels of Pten, p16, p21 and p53 also elevated with increased age. Immuno-fluorescence analysis showed that Akt phosphorylation found in the epidermal cells (with increased levels of NF-κB activation) were also found. In vivo inhibition of AKT activity result in reduced NF-κB activation. Our results suggest that increasing Akt/ NF-κB is a crucial mediator of skin aging, which can increase the susceptibility of cell transformation. |
format | Online Article Text |
id | pubmed-5462418 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-54624182017-06-22 AKT and its related molecular feature in aged mice skin Chen, Haiyan Wang, Xusheng Han, Jimin Fan, Zhimeng Sadia, Sobia Zhang, Rongrong Guo, Yingsheng Jiang, Yuyang Wu, Yaojiong PLoS One Research Article Previous studies suggest that Akt signaling promotes tissue regeneration and decreased Akt activities are found in aged tissues. However, this study finds that the expression and activation levels of Akt in the mice skin increased with age. Additionally, the expression levels of Pten, p16, p21 and p53 also elevated with increased age. Immuno-fluorescence analysis showed that Akt phosphorylation found in the epidermal cells (with increased levels of NF-κB activation) were also found. In vivo inhibition of AKT activity result in reduced NF-κB activation. Our results suggest that increasing Akt/ NF-κB is a crucial mediator of skin aging, which can increase the susceptibility of cell transformation. Public Library of Science 2017-06-07 /pmc/articles/PMC5462418/ /pubmed/28591208 http://dx.doi.org/10.1371/journal.pone.0178969 Text en © 2017 Chen 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Chen, Haiyan Wang, Xusheng Han, Jimin Fan, Zhimeng Sadia, Sobia Zhang, Rongrong Guo, Yingsheng Jiang, Yuyang Wu, Yaojiong AKT and its related molecular feature in aged mice skin |
title | AKT and its related molecular feature in aged mice skin |
title_full | AKT and its related molecular feature in aged mice skin |
title_fullStr | AKT and its related molecular feature in aged mice skin |
title_full_unstemmed | AKT and its related molecular feature in aged mice skin |
title_short | AKT and its related molecular feature in aged mice skin |
title_sort | akt and its related molecular feature in aged mice skin |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5462418/ https://www.ncbi.nlm.nih.gov/pubmed/28591208 http://dx.doi.org/10.1371/journal.pone.0178969 |
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