Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Barkho, Basam Z., Monuki, Edwin S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
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
_version_ 1782363803475771392
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
work_keys_str_mv AT barkhobasamz proliferationofculturedmousechoroidplexusepithelialcells
AT monukiedwins proliferationofculturedmousechoroidplexusepithelialcells