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The Insulin-Like Growth Factor System in the Long-Lived Naked Mole-Rat
Naked mole-rats (Heterocephalus glaber) (NMRs) are the longest living rodents known. They show negligible senescence, and are resistant to cancers and certain damaging effects associated with aging. The insulin-like growth factors (IGFs) have pluripotent actions, influencing growth processes in virt...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4694111/ https://www.ncbi.nlm.nih.gov/pubmed/26694858 http://dx.doi.org/10.1371/journal.pone.0145587 |
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author | Brohus, Malene Gorbunova, Vera Faulkes, Chris G. Overgaard, Michael T. Conover, Cheryl A. |
author_facet | Brohus, Malene Gorbunova, Vera Faulkes, Chris G. Overgaard, Michael T. Conover, Cheryl A. |
author_sort | Brohus, Malene |
collection | PubMed |
description | Naked mole-rats (Heterocephalus glaber) (NMRs) are the longest living rodents known. They show negligible senescence, and are resistant to cancers and certain damaging effects associated with aging. The insulin-like growth factors (IGFs) have pluripotent actions, influencing growth processes in virtually every system of the body. They are established contributors to the aging process, confirmed by the demonstration that decreased IGF signaling results in life-extending effects in a variety of species. The IGFs are likewise involved in progression of cancers by mediating survival signals in malignant cells. This report presents a full characterization of the IGF system in the NMR: ligands, receptors, IGF binding proteins (IGFBPs), and IGFBP proteases. A particular emphasis was placed on the IGFBP protease, pregnancy-associated plasma protein-A (PAPP-A), shown to be an important lifespan modulator in mice. Comparisons of IGF-related genes in the NMR with human and murine sequences indicated no major differences in essential parts of the IGF system, including PAPP-A. The protease was shown to possess an intact active site despite the report of a contradictory genome sequence. Furthermore, PAPP-A was expressed and translated in NMRs cells and retained IGF-dependent proteolytic activity towards IGFBP-4 and IGF-independent activity towards IGFBP-5. However, experimental data suggest differential regulatory mechanisms for PAPP-A expression in NMRs than those described in humans and mice. This overall description of the IGF system in the NMR represents an initial step towards elucidating the complex molecular mechanisms underlying longevity, and how these animals have evolved to ensure a delayed and healthy aging process. |
format | Online Article Text |
id | pubmed-4694111 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-46941112016-01-07 The Insulin-Like Growth Factor System in the Long-Lived Naked Mole-Rat Brohus, Malene Gorbunova, Vera Faulkes, Chris G. Overgaard, Michael T. Conover, Cheryl A. PLoS One Research Article Naked mole-rats (Heterocephalus glaber) (NMRs) are the longest living rodents known. They show negligible senescence, and are resistant to cancers and certain damaging effects associated with aging. The insulin-like growth factors (IGFs) have pluripotent actions, influencing growth processes in virtually every system of the body. They are established contributors to the aging process, confirmed by the demonstration that decreased IGF signaling results in life-extending effects in a variety of species. The IGFs are likewise involved in progression of cancers by mediating survival signals in malignant cells. This report presents a full characterization of the IGF system in the NMR: ligands, receptors, IGF binding proteins (IGFBPs), and IGFBP proteases. A particular emphasis was placed on the IGFBP protease, pregnancy-associated plasma protein-A (PAPP-A), shown to be an important lifespan modulator in mice. Comparisons of IGF-related genes in the NMR with human and murine sequences indicated no major differences in essential parts of the IGF system, including PAPP-A. The protease was shown to possess an intact active site despite the report of a contradictory genome sequence. Furthermore, PAPP-A was expressed and translated in NMRs cells and retained IGF-dependent proteolytic activity towards IGFBP-4 and IGF-independent activity towards IGFBP-5. However, experimental data suggest differential regulatory mechanisms for PAPP-A expression in NMRs than those described in humans and mice. This overall description of the IGF system in the NMR represents an initial step towards elucidating the complex molecular mechanisms underlying longevity, and how these animals have evolved to ensure a delayed and healthy aging process. Public Library of Science 2015-12-22 /pmc/articles/PMC4694111/ /pubmed/26694858 http://dx.doi.org/10.1371/journal.pone.0145587 Text en © 2015 Brohus 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Brohus, Malene Gorbunova, Vera Faulkes, Chris G. Overgaard, Michael T. Conover, Cheryl A. The Insulin-Like Growth Factor System in the Long-Lived Naked Mole-Rat |
title | The Insulin-Like Growth Factor System in the Long-Lived Naked Mole-Rat |
title_full | The Insulin-Like Growth Factor System in the Long-Lived Naked Mole-Rat |
title_fullStr | The Insulin-Like Growth Factor System in the Long-Lived Naked Mole-Rat |
title_full_unstemmed | The Insulin-Like Growth Factor System in the Long-Lived Naked Mole-Rat |
title_short | The Insulin-Like Growth Factor System in the Long-Lived Naked Mole-Rat |
title_sort | insulin-like growth factor system in the long-lived naked mole-rat |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4694111/ https://www.ncbi.nlm.nih.gov/pubmed/26694858 http://dx.doi.org/10.1371/journal.pone.0145587 |
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