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Expression of transient receptor potential channels in the ependymal cells of the developing rat brain
Cerebrospinal fluid (CSF) plays an important role in providing brain tissue with a stable internal environment as well as in absorbing mechanical and thermal stresses. From its initial composition, derived from the amniotic fluid trapped by the closure of neuropores, CSF is modified by developing an...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Association of Anatomists
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3615614/ https://www.ncbi.nlm.nih.gov/pubmed/23560238 http://dx.doi.org/10.5115/acb.2013.46.1.68 |
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author | Jo, Kwang Deog Lee, Kyu-Seok Lee, Won Taek Hur, Mi-Sun Kim, Ho-Jeong |
author_facet | Jo, Kwang Deog Lee, Kyu-Seok Lee, Won Taek Hur, Mi-Sun Kim, Ho-Jeong |
author_sort | Jo, Kwang Deog |
collection | PubMed |
description | Cerebrospinal fluid (CSF) plays an important role in providing brain tissue with a stable internal environment as well as in absorbing mechanical and thermal stresses. From its initial composition, derived from the amniotic fluid trapped by the closure of neuropores, CSF is modified by developing and differentiating ependymal cells lining the ventricular surface or forming the choroid plexus. Its osmolarity and ionic composition brings about a change through the action of many channels expressed on the ependymal cells. Some newly discovered transient receptor potential (TRP) channels are known to be expressed in the choroid plexus ependyma. To detect additional TRP channel expression, immunohistochemical screening was performed at the choroid plexus of 13-, 15-, 17-, and 19-day embryos, using antibodies against TRPV1, TRPV3, and TRPA1, and the expression was compared with those in the adult TRP channels. The level of TRP channel expression was higher in the choroid plexus which suggests more active functioning of TRP channels in the developing choroid plexus than the ventricular lining ependyma in the 15- and 17-day embryos. All the expression of TRP channels decreased at the 19th day of gestation. TRPA1 was expressed at a higher level than TRPV1 and TRPV3 in almost all stages in both the choroid plexus and ventricular lining epithelium. The highest level of TRPV1 and TRPV3 expression was observed in association with the glycogen deposits in the cytoplasm of the choroid plexus ependymal cells of the 15- and 17-day embryos. |
format | Online Article Text |
id | pubmed-3615614 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Korean Association of Anatomists |
record_format | MEDLINE/PubMed |
spelling | pubmed-36156142013-04-04 Expression of transient receptor potential channels in the ependymal cells of the developing rat brain Jo, Kwang Deog Lee, Kyu-Seok Lee, Won Taek Hur, Mi-Sun Kim, Ho-Jeong Anat Cell Biol Original Article Cerebrospinal fluid (CSF) plays an important role in providing brain tissue with a stable internal environment as well as in absorbing mechanical and thermal stresses. From its initial composition, derived from the amniotic fluid trapped by the closure of neuropores, CSF is modified by developing and differentiating ependymal cells lining the ventricular surface or forming the choroid plexus. Its osmolarity and ionic composition brings about a change through the action of many channels expressed on the ependymal cells. Some newly discovered transient receptor potential (TRP) channels are known to be expressed in the choroid plexus ependyma. To detect additional TRP channel expression, immunohistochemical screening was performed at the choroid plexus of 13-, 15-, 17-, and 19-day embryos, using antibodies against TRPV1, TRPV3, and TRPA1, and the expression was compared with those in the adult TRP channels. The level of TRP channel expression was higher in the choroid plexus which suggests more active functioning of TRP channels in the developing choroid plexus than the ventricular lining ependyma in the 15- and 17-day embryos. All the expression of TRP channels decreased at the 19th day of gestation. TRPA1 was expressed at a higher level than TRPV1 and TRPV3 in almost all stages in both the choroid plexus and ventricular lining epithelium. The highest level of TRPV1 and TRPV3 expression was observed in association with the glycogen deposits in the cytoplasm of the choroid plexus ependymal cells of the 15- and 17-day embryos. Korean Association of Anatomists 2013-03 2013-03-25 /pmc/articles/PMC3615614/ /pubmed/23560238 http://dx.doi.org/10.5115/acb.2013.46.1.68 Text en Copyright © 2013. Anatomy & Cell Biology http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Jo, Kwang Deog Lee, Kyu-Seok Lee, Won Taek Hur, Mi-Sun Kim, Ho-Jeong Expression of transient receptor potential channels in the ependymal cells of the developing rat brain |
title | Expression of transient receptor potential channels in the ependymal cells of the developing rat brain |
title_full | Expression of transient receptor potential channels in the ependymal cells of the developing rat brain |
title_fullStr | Expression of transient receptor potential channels in the ependymal cells of the developing rat brain |
title_full_unstemmed | Expression of transient receptor potential channels in the ependymal cells of the developing rat brain |
title_short | Expression of transient receptor potential channels in the ependymal cells of the developing rat brain |
title_sort | expression of transient receptor potential channels in the ependymal cells of the developing rat brain |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3615614/ https://www.ncbi.nlm.nih.gov/pubmed/23560238 http://dx.doi.org/10.5115/acb.2013.46.1.68 |
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