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Protracted brain development in a rodent model of extreme longevity

Extreme longevity requires the continuous and large-scale adaptation of organ systems to delay senescence. Naked mole rats are the longest-living rodents, whose nervous system likely undergoes life-long adaptive reorganization. Nevertheless, neither the cellular organization of their cerebral cortex...

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Autores principales: Penz, Orsolya K., Fuzik, Janos, Kurek, Aleksandra B., Romanov, Roman, Larson, John, Park, Thomas J., Harkany, Tibor, Keimpema, Erik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4484490/
https://www.ncbi.nlm.nih.gov/pubmed/26118676
http://dx.doi.org/10.1038/srep11592
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author Penz, Orsolya K.
Fuzik, Janos
Kurek, Aleksandra B.
Romanov, Roman
Larson, John
Park, Thomas J.
Harkany, Tibor
Keimpema, Erik
author_facet Penz, Orsolya K.
Fuzik, Janos
Kurek, Aleksandra B.
Romanov, Roman
Larson, John
Park, Thomas J.
Harkany, Tibor
Keimpema, Erik
author_sort Penz, Orsolya K.
collection PubMed
description Extreme longevity requires the continuous and large-scale adaptation of organ systems to delay senescence. Naked mole rats are the longest-living rodents, whose nervous system likely undergoes life-long adaptive reorganization. Nevertheless, neither the cellular organization of their cerebral cortex nor indices of structural neuronal plasticity along extreme time-scales have been established. We find that adult neurogenesis and neuronal migration are not unusual in naked mole rat brains. Instead, we show the prolonged expression of structural plasticity markers, many recognized as being developmentally controlled, and multi-year-long postnatal neuromorphogenesis and spatial synapse refinement in hippocampal and olfactory structures of the naked mole rat brain. Neurophysiological studies on identified hippocampal neurons demonstrated that morphological differentiation is disconnected from the control of excitability in all neuronal contingents regardless of their ability to self-renew. Overall, we conclude that naked mole rats show an extremely protracted period of brain maturation that may permit plasticity and resilience to neurodegenerative processes over their decades-long life span. This conclusion is consistent with the hypothesis that naked mole rats are neotenous, with retention of juvenile characteristics to permit survival in a hypoxic environment, with extreme longevity a consequence of greatly retarded development.
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spelling pubmed-44844902015-07-08 Protracted brain development in a rodent model of extreme longevity Penz, Orsolya K. Fuzik, Janos Kurek, Aleksandra B. Romanov, Roman Larson, John Park, Thomas J. Harkany, Tibor Keimpema, Erik Sci Rep Article Extreme longevity requires the continuous and large-scale adaptation of organ systems to delay senescence. Naked mole rats are the longest-living rodents, whose nervous system likely undergoes life-long adaptive reorganization. Nevertheless, neither the cellular organization of their cerebral cortex nor indices of structural neuronal plasticity along extreme time-scales have been established. We find that adult neurogenesis and neuronal migration are not unusual in naked mole rat brains. Instead, we show the prolonged expression of structural plasticity markers, many recognized as being developmentally controlled, and multi-year-long postnatal neuromorphogenesis and spatial synapse refinement in hippocampal and olfactory structures of the naked mole rat brain. Neurophysiological studies on identified hippocampal neurons demonstrated that morphological differentiation is disconnected from the control of excitability in all neuronal contingents regardless of their ability to self-renew. Overall, we conclude that naked mole rats show an extremely protracted period of brain maturation that may permit plasticity and resilience to neurodegenerative processes over their decades-long life span. This conclusion is consistent with the hypothesis that naked mole rats are neotenous, with retention of juvenile characteristics to permit survival in a hypoxic environment, with extreme longevity a consequence of greatly retarded development. Nature Publishing Group 2015-06-29 /pmc/articles/PMC4484490/ /pubmed/26118676 http://dx.doi.org/10.1038/srep11592 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Penz, Orsolya K.
Fuzik, Janos
Kurek, Aleksandra B.
Romanov, Roman
Larson, John
Park, Thomas J.
Harkany, Tibor
Keimpema, Erik
Protracted brain development in a rodent model of extreme longevity
title Protracted brain development in a rodent model of extreme longevity
title_full Protracted brain development in a rodent model of extreme longevity
title_fullStr Protracted brain development in a rodent model of extreme longevity
title_full_unstemmed Protracted brain development in a rodent model of extreme longevity
title_short Protracted brain development in a rodent model of extreme longevity
title_sort protracted brain development in a rodent model of extreme longevity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4484490/
https://www.ncbi.nlm.nih.gov/pubmed/26118676
http://dx.doi.org/10.1038/srep11592
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