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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...

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Autores principales: Lee, Seung-Hee, Itkin-Ansari, Pamela, Levine, Fred
Formato: Texto
Lenguaje:English
Publicado: Impact Journals LLC 2010
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.
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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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