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CENP-A, a protein required for chromosome segregation in mitosis, declines with age in islet but not exocrine cells
Beta-cell replication dramatically declines with age. Here, we report that the level of CENP-A, a protein required for cell division, declines precipitously with age in an islet-specific manner. CENP-A is essentially undetectable after age 29 in humans. However, exocrine cells retain CENP-A expressi...
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
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Impact Journals LLC
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3006021/ https://www.ncbi.nlm.nih.gov/pubmed/21068465 |
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author | Lee, Seung-Hee Itkin-Ansari, Pamela Levine, Fred |
author_facet | Lee, Seung-Hee Itkin-Ansari, Pamela Levine, Fred |
author_sort | Lee, Seung-Hee |
collection | PubMed |
description | Beta-cell replication dramatically declines with age. Here, we report that the level of CENP-A, a protein required for cell division, declines precipitously with age in an islet-specific manner. CENP-A is essentially undetectable after age 29 in humans. However, exocrine cells retain CENP-A expression. The decline in islet-cell CENP-A expression is more striking in humans than in mice, where CENP-A expression continues to be detectable at low levels even in elderly mice. The mechanism by which CENP-A declines appears to be post-transcriptional, as there was no correlation between CENP-A mRNA levels and age or islet purity. This finding has implications for efforts to induce beta-cell replication as a treatment for diabetes. |
format | Text |
id | pubmed-3006021 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-30060212010-12-22 CENP-A, a protein required for chromosome segregation in mitosis, declines with age in islet but not exocrine cells Lee, Seung-Hee Itkin-Ansari, Pamela Levine, Fred Aging (Albany NY) Research Paper Beta-cell replication dramatically declines with age. Here, we report that the level of CENP-A, a protein required for cell division, declines precipitously with age in an islet-specific manner. CENP-A is essentially undetectable after age 29 in humans. However, exocrine cells retain CENP-A expression. The decline in islet-cell CENP-A expression is more striking in humans than in mice, where CENP-A expression continues to be detectable at low levels even in elderly mice. The mechanism by which CENP-A declines appears to be post-transcriptional, as there was no correlation between CENP-A mRNA levels and age or islet purity. This finding has implications for efforts to induce beta-cell replication as a treatment for diabetes. Impact Journals LLC 2010-10-29 /pmc/articles/PMC3006021/ /pubmed/21068465 Text en Copyright: © 2010 Lee 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 Lee, Seung-Hee Itkin-Ansari, Pamela Levine, Fred CENP-A, a protein required for chromosome segregation in mitosis, declines with age in islet but not exocrine cells |
title | CENP-A, a protein required for chromosome segregation in mitosis, declines with age in islet but not exocrine cells |
title_full | CENP-A, a protein required for chromosome segregation in mitosis, declines with age in islet but not exocrine cells |
title_fullStr | CENP-A, a protein required for chromosome segregation in mitosis, declines with age in islet but not exocrine cells |
title_full_unstemmed | CENP-A, a protein required for chromosome segregation in mitosis, declines with age in islet but not exocrine cells |
title_short | CENP-A, a protein required for chromosome segregation in mitosis, declines with age in islet but not exocrine cells |
title_sort | cenp-a, a protein required for chromosome segregation in mitosis, declines with age in islet but not exocrine cells |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3006021/ https://www.ncbi.nlm.nih.gov/pubmed/21068465 |
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