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Premature Neural Progenitor Cell Differentiation Into Astrocytes in Retinoic Acid-Induced Spina Bifida Rat Model

During embryonic spinal cord development, neural progenitor cells (NPCs) generate three major cell lines: neurons, oligodendrocytes, and astrocytes at precise times and locations within the spinal cord. Recent studies demonstrate early astrogenesis in animal models of spina bifida, which may play a...

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Autores principales: Oria, Marc, Pathak, Bedika, Li, Zhen, Bakri, Kenan, Gouwens, Kara, Varela, Maria Florencia, Lampe, Kristin, Murphy, Kendall P., Lin, Chia-Ying, Peiro, Jose L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9249056/
https://www.ncbi.nlm.nih.gov/pubmed/35782393
http://dx.doi.org/10.3389/fnmol.2022.888351
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author Oria, Marc
Pathak, Bedika
Li, Zhen
Bakri, Kenan
Gouwens, Kara
Varela, Maria Florencia
Lampe, Kristin
Murphy, Kendall P.
Lin, Chia-Ying
Peiro, Jose L.
author_facet Oria, Marc
Pathak, Bedika
Li, Zhen
Bakri, Kenan
Gouwens, Kara
Varela, Maria Florencia
Lampe, Kristin
Murphy, Kendall P.
Lin, Chia-Ying
Peiro, Jose L.
author_sort Oria, Marc
collection PubMed
description During embryonic spinal cord development, neural progenitor cells (NPCs) generate three major cell lines: neurons, oligodendrocytes, and astrocytes at precise times and locations within the spinal cord. Recent studies demonstrate early astrogenesis in animal models of spina bifida, which may play a role in neuronal dysfunction associated with this condition. However, to date, the pathophysiological mechanisms related to this early astrocytic response in spina bifida are poorly understood. This study aimed to characterize the development of early astrogliosis over time from Pax6+, Olig2+, or Nkx2.2+ NPCs using a retinoic acid-induced spina bifida rat model. At three gestational ages (E15, E17, and E20), spinal cords from fetuses with retinoic acid-induced spina bifida, their healthy sibling controls, or fetuses treated with the vehicle control were analyzed. Results indicated that premature astrogliosis and astrocytic activation were associated with an altered presence of Pax6+, Olig2+, and Nkx2.2+ NPCs in the lesion compared to the controls. Finally, this response correlated with an elevation in genes involved in the Notch-BMP signaling pathway. Taken together, changes in NPC patterning factor expression with Notch-BMP signaling upregulation may be responsible for the altered astrogenesis patterns observed in the spinal cord in a retinoic acid-induced spina bifida model.
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spelling pubmed-92490562022-07-02 Premature Neural Progenitor Cell Differentiation Into Astrocytes in Retinoic Acid-Induced Spina Bifida Rat Model Oria, Marc Pathak, Bedika Li, Zhen Bakri, Kenan Gouwens, Kara Varela, Maria Florencia Lampe, Kristin Murphy, Kendall P. Lin, Chia-Ying Peiro, Jose L. Front Mol Neurosci Neuroscience During embryonic spinal cord development, neural progenitor cells (NPCs) generate three major cell lines: neurons, oligodendrocytes, and astrocytes at precise times and locations within the spinal cord. Recent studies demonstrate early astrogenesis in animal models of spina bifida, which may play a role in neuronal dysfunction associated with this condition. However, to date, the pathophysiological mechanisms related to this early astrocytic response in spina bifida are poorly understood. This study aimed to characterize the development of early astrogliosis over time from Pax6+, Olig2+, or Nkx2.2+ NPCs using a retinoic acid-induced spina bifida rat model. At three gestational ages (E15, E17, and E20), spinal cords from fetuses with retinoic acid-induced spina bifida, their healthy sibling controls, or fetuses treated with the vehicle control were analyzed. Results indicated that premature astrogliosis and astrocytic activation were associated with an altered presence of Pax6+, Olig2+, and Nkx2.2+ NPCs in the lesion compared to the controls. Finally, this response correlated with an elevation in genes involved in the Notch-BMP signaling pathway. Taken together, changes in NPC patterning factor expression with Notch-BMP signaling upregulation may be responsible for the altered astrogenesis patterns observed in the spinal cord in a retinoic acid-induced spina bifida model. Frontiers Media S.A. 2022-06-17 /pmc/articles/PMC9249056/ /pubmed/35782393 http://dx.doi.org/10.3389/fnmol.2022.888351 Text en Copyright © 2022 Oria, Pathak, Li, Bakri, Gouwens, Varela, Lampe, Murphy, Lin and Peiro. https://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) and the copyright owner(s) 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
Oria, Marc
Pathak, Bedika
Li, Zhen
Bakri, Kenan
Gouwens, Kara
Varela, Maria Florencia
Lampe, Kristin
Murphy, Kendall P.
Lin, Chia-Ying
Peiro, Jose L.
Premature Neural Progenitor Cell Differentiation Into Astrocytes in Retinoic Acid-Induced Spina Bifida Rat Model
title Premature Neural Progenitor Cell Differentiation Into Astrocytes in Retinoic Acid-Induced Spina Bifida Rat Model
title_full Premature Neural Progenitor Cell Differentiation Into Astrocytes in Retinoic Acid-Induced Spina Bifida Rat Model
title_fullStr Premature Neural Progenitor Cell Differentiation Into Astrocytes in Retinoic Acid-Induced Spina Bifida Rat Model
title_full_unstemmed Premature Neural Progenitor Cell Differentiation Into Astrocytes in Retinoic Acid-Induced Spina Bifida Rat Model
title_short Premature Neural Progenitor Cell Differentiation Into Astrocytes in Retinoic Acid-Induced Spina Bifida Rat Model
title_sort premature neural progenitor cell differentiation into astrocytes in retinoic acid-induced spina bifida rat model
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9249056/
https://www.ncbi.nlm.nih.gov/pubmed/35782393
http://dx.doi.org/10.3389/fnmol.2022.888351
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