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Injury in aged animals robustly activates quiescent olfactory neural stem cells

While the capacity of the olfactory epithelium (OE) to generate sensory neurons continues into middle age in mice, it is presumed that this regenerative potential is present throughout all developmental stages. However, little experimental evidence exists to support the idea that this regenerative c...

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Autores principales: Brann, Jessica H., Ellis, Deandrea P., Ku, Benson S., Spinazzi, Eleonora F., Firestein, Stuart
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4596941/
https://www.ncbi.nlm.nih.gov/pubmed/26500487
http://dx.doi.org/10.3389/fnins.2015.00367
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author Brann, Jessica H.
Ellis, Deandrea P.
Ku, Benson S.
Spinazzi, Eleonora F.
Firestein, Stuart
author_facet Brann, Jessica H.
Ellis, Deandrea P.
Ku, Benson S.
Spinazzi, Eleonora F.
Firestein, Stuart
author_sort Brann, Jessica H.
collection PubMed
description While the capacity of the olfactory epithelium (OE) to generate sensory neurons continues into middle age in mice, it is presumed that this regenerative potential is present throughout all developmental stages. However, little experimental evidence exists to support the idea that this regenerative capacity remains in late adulthood, and questions about the functionality of neurons born at these late stages remain unanswered. Here, we extend our previous work in the VNO to investigate basal rates of proliferation in the OE, as well as after olfactory bulbectomy (OBX), a commonly used surgical lesion. In addition, we show that the neural stem cell retains its capacity to generate mature olfactory sensory neurons in aged animals. Finally, we demonstrate that regardless of age, a stem cell in the OE, the horizontal basal cell (HBC), exhibits a morphological switch from a flattened, quiescent phenotype to a pyramidal, proliferative phenotype following chemical lesion in aged animals. These findings provide new insights into determining whether an HBC is active or quiescent based on a structural feature as opposed to a biochemical one. More importantly, it suggests that neural stem cells in aged mice are responsive to the same signals triggering proliferation as those observed in young mice.
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spelling pubmed-45969412015-10-23 Injury in aged animals robustly activates quiescent olfactory neural stem cells Brann, Jessica H. Ellis, Deandrea P. Ku, Benson S. Spinazzi, Eleonora F. Firestein, Stuart Front Neurosci Neuroscience While the capacity of the olfactory epithelium (OE) to generate sensory neurons continues into middle age in mice, it is presumed that this regenerative potential is present throughout all developmental stages. However, little experimental evidence exists to support the idea that this regenerative capacity remains in late adulthood, and questions about the functionality of neurons born at these late stages remain unanswered. Here, we extend our previous work in the VNO to investigate basal rates of proliferation in the OE, as well as after olfactory bulbectomy (OBX), a commonly used surgical lesion. In addition, we show that the neural stem cell retains its capacity to generate mature olfactory sensory neurons in aged animals. Finally, we demonstrate that regardless of age, a stem cell in the OE, the horizontal basal cell (HBC), exhibits a morphological switch from a flattened, quiescent phenotype to a pyramidal, proliferative phenotype following chemical lesion in aged animals. These findings provide new insights into determining whether an HBC is active or quiescent based on a structural feature as opposed to a biochemical one. More importantly, it suggests that neural stem cells in aged mice are responsive to the same signals triggering proliferation as those observed in young mice. Frontiers Media S.A. 2015-10-08 /pmc/articles/PMC4596941/ /pubmed/26500487 http://dx.doi.org/10.3389/fnins.2015.00367 Text en Copyright © 2015 Brann, Ellis, Ku, Spinazzi and Firestein. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Brann, Jessica H.
Ellis, Deandrea P.
Ku, Benson S.
Spinazzi, Eleonora F.
Firestein, Stuart
Injury in aged animals robustly activates quiescent olfactory neural stem cells
title Injury in aged animals robustly activates quiescent olfactory neural stem cells
title_full Injury in aged animals robustly activates quiescent olfactory neural stem cells
title_fullStr Injury in aged animals robustly activates quiescent olfactory neural stem cells
title_full_unstemmed Injury in aged animals robustly activates quiescent olfactory neural stem cells
title_short Injury in aged animals robustly activates quiescent olfactory neural stem cells
title_sort injury in aged animals robustly activates quiescent olfactory neural stem cells
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4596941/
https://www.ncbi.nlm.nih.gov/pubmed/26500487
http://dx.doi.org/10.3389/fnins.2015.00367
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