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The tissue dependent interactions between p53 and Bcl-2 in vivo
To further investigate the role of p53 in apoptosis in vivo and the interaction between p53 and Bcl-2 in the regulation of cellular apoptosis in vivo, we depleted p53 in Bcl-2-null mice. We found that the interaction between p53 and Bcl-2 are tissue dependent. Specifically, loss of p53 in Bcl-2(−/−)...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4742135/ https://www.ncbi.nlm.nih.gov/pubmed/26452131 |
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author | Li, Xin Miao, Xiao Wang, Hongshen Xu, Zhixiang Li, Bin |
author_facet | Li, Xin Miao, Xiao Wang, Hongshen Xu, Zhixiang Li, Bin |
author_sort | Li, Xin |
collection | PubMed |
description | To further investigate the role of p53 in apoptosis in vivo and the interaction between p53 and Bcl-2 in the regulation of cellular apoptosis in vivo, we depleted p53 in Bcl-2-null mice. We found that the interaction between p53 and Bcl-2 are tissue dependent. Specifically, loss of p53 in Bcl-2(−/−) mice inhibits apoptotic induction in spleen and subsequently inhibits the Bcl-2-null-induced spleen atrophy. Furthermore, p53 deficiency overcomes loss of melanocyte stem cell (MSC)-induced apoptosis and subsequently prevents hair graying in Bcl-2- null mice. In addition, p53 deletion partly inhibits apoptosis in hair follicle keratinocytes, leading to the alleviation of hair growth delay in Bcl-2-null mice. However, p53 absence in Bcl-2-null mice cannot restore other defects in Bcl-2-null mice, including retardation of growth, short ears and polycystic kidney disease. |
format | Online Article Text |
id | pubmed-4742135 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-47421352016-04-04 The tissue dependent interactions between p53 and Bcl-2 in vivo Li, Xin Miao, Xiao Wang, Hongshen Xu, Zhixiang Li, Bin Oncotarget Research Paper To further investigate the role of p53 in apoptosis in vivo and the interaction between p53 and Bcl-2 in the regulation of cellular apoptosis in vivo, we depleted p53 in Bcl-2-null mice. We found that the interaction between p53 and Bcl-2 are tissue dependent. Specifically, loss of p53 in Bcl-2(−/−) mice inhibits apoptotic induction in spleen and subsequently inhibits the Bcl-2-null-induced spleen atrophy. Furthermore, p53 deficiency overcomes loss of melanocyte stem cell (MSC)-induced apoptosis and subsequently prevents hair graying in Bcl-2- null mice. In addition, p53 deletion partly inhibits apoptosis in hair follicle keratinocytes, leading to the alleviation of hair growth delay in Bcl-2-null mice. However, p53 absence in Bcl-2-null mice cannot restore other defects in Bcl-2-null mice, including retardation of growth, short ears and polycystic kidney disease. Impact Journals LLC 2015-10-06 /pmc/articles/PMC4742135/ /pubmed/26452131 Text en Copyright: © 2015 Li et al. http://creativecommons.org/licenses/by/2.5/ 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 credited. |
spellingShingle | Research Paper Li, Xin Miao, Xiao Wang, Hongshen Xu, Zhixiang Li, Bin The tissue dependent interactions between p53 and Bcl-2 in vivo |
title | The tissue dependent interactions between p53 and Bcl-2 in vivo |
title_full | The tissue dependent interactions between p53 and Bcl-2 in vivo |
title_fullStr | The tissue dependent interactions between p53 and Bcl-2 in vivo |
title_full_unstemmed | The tissue dependent interactions between p53 and Bcl-2 in vivo |
title_short | The tissue dependent interactions between p53 and Bcl-2 in vivo |
title_sort | tissue dependent interactions between p53 and bcl-2 in vivo |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4742135/ https://www.ncbi.nlm.nih.gov/pubmed/26452131 |
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