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Proliferation of Cultured Mouse Choroid Plexus Epithelial Cells
The choroid plexus (ChP) epithelium is a multifunctional tissue found in the ventricles of the brain. The major function of the ChP epithelium is to produce cerebrospinal fluid (CSF) that bathes and nourishes the central nervous system (CNS). In addition to the CSF, ChP epithelial cells (CPECs) prod...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4376882/ https://www.ncbi.nlm.nih.gov/pubmed/25815836 http://dx.doi.org/10.1371/journal.pone.0121738 |
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author | Barkho, Basam Z. Monuki, Edwin S. |
author_facet | Barkho, Basam Z. Monuki, Edwin S. |
author_sort | Barkho, Basam Z. |
collection | PubMed |
description | The choroid plexus (ChP) epithelium is a multifunctional tissue found in the ventricles of the brain. The major function of the ChP epithelium is to produce cerebrospinal fluid (CSF) that bathes and nourishes the central nervous system (CNS). In addition to the CSF, ChP epithelial cells (CPECs) produce and secrete numerous neurotrophic factors that support brain homeostasis, such as adult hippocampal neurogenesis. Accordingly, damage and dysfunction to CPECs are thought to accelerate and intensify multiple disease phenotypes, and CPEC regeneration would represent a potential therapeutic approach for these diseases. However, previous reports suggest that CPECs rarely divide, although this has not been extensively studied in response to extrinsic factors. Utilizing a cell-cycle reporter mouse line and live cell imaging, we identified scratch injury and the growth factors insulin-like growth factor 1 (IGF-1) and epidermal growth factor (EGF) as extrinsic cues that promote increased CPEC expansion in vitro. Furthermore, we found that IGF-1 and EGF treatment enhances scratch injury-induced proliferation. Finally, we established whole tissue explant cultures and observed that IGF-1 and EGF promote CPEC division within the intact ChP epithelium. We conclude that although CPECs normally have a slow turnover rate, they expand in response to external stimuli such as injury and/or growth factors, which provides a potential avenue for enhancing ChP function after brain injury or neurodegeneration. |
format | Online Article Text |
id | pubmed-4376882 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-43768822015-04-04 Proliferation of Cultured Mouse Choroid Plexus Epithelial Cells Barkho, Basam Z. Monuki, Edwin S. PLoS One Research Article The choroid plexus (ChP) epithelium is a multifunctional tissue found in the ventricles of the brain. The major function of the ChP epithelium is to produce cerebrospinal fluid (CSF) that bathes and nourishes the central nervous system (CNS). In addition to the CSF, ChP epithelial cells (CPECs) produce and secrete numerous neurotrophic factors that support brain homeostasis, such as adult hippocampal neurogenesis. Accordingly, damage and dysfunction to CPECs are thought to accelerate and intensify multiple disease phenotypes, and CPEC regeneration would represent a potential therapeutic approach for these diseases. However, previous reports suggest that CPECs rarely divide, although this has not been extensively studied in response to extrinsic factors. Utilizing a cell-cycle reporter mouse line and live cell imaging, we identified scratch injury and the growth factors insulin-like growth factor 1 (IGF-1) and epidermal growth factor (EGF) as extrinsic cues that promote increased CPEC expansion in vitro. Furthermore, we found that IGF-1 and EGF treatment enhances scratch injury-induced proliferation. Finally, we established whole tissue explant cultures and observed that IGF-1 and EGF promote CPEC division within the intact ChP epithelium. We conclude that although CPECs normally have a slow turnover rate, they expand in response to external stimuli such as injury and/or growth factors, which provides a potential avenue for enhancing ChP function after brain injury or neurodegeneration. Public Library of Science 2015-03-27 /pmc/articles/PMC4376882/ /pubmed/25815836 http://dx.doi.org/10.1371/journal.pone.0121738 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. |
spellingShingle | Research Article Barkho, Basam Z. Monuki, Edwin S. Proliferation of Cultured Mouse Choroid Plexus Epithelial Cells |
title | Proliferation of Cultured Mouse Choroid Plexus Epithelial Cells |
title_full | Proliferation of Cultured Mouse Choroid Plexus Epithelial Cells |
title_fullStr | Proliferation of Cultured Mouse Choroid Plexus Epithelial Cells |
title_full_unstemmed | Proliferation of Cultured Mouse Choroid Plexus Epithelial Cells |
title_short | Proliferation of Cultured Mouse Choroid Plexus Epithelial Cells |
title_sort | proliferation of cultured mouse choroid plexus epithelial cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4376882/ https://www.ncbi.nlm.nih.gov/pubmed/25815836 http://dx.doi.org/10.1371/journal.pone.0121738 |
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