Cargando…
Ependymal cells of the mouse brain express urate transporter 1 (URAT1)
BACKGROUND: Elevated uric acid (UA) is commonly associated with gout and it is also a known cardiovascular disease risk factor. In contrast to such deleterious effects, UA possesses neuroprotective properties in the brain and elucidating the molecular mechanisms involved may have significant value r...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4015888/ https://www.ncbi.nlm.nih.gov/pubmed/24156345 http://dx.doi.org/10.1186/2045-8118-10-31 |
_version_ | 1782315420927131648 |
---|---|
author | Tomioka, Naoko H Nakamura, Makiko Doshi, Masaru Deguchi, Yoshiharu Ichida, Kimiyoshi Morisaki, Takayuki Hosoyamada, Makoto |
author_facet | Tomioka, Naoko H Nakamura, Makiko Doshi, Masaru Deguchi, Yoshiharu Ichida, Kimiyoshi Morisaki, Takayuki Hosoyamada, Makoto |
author_sort | Tomioka, Naoko H |
collection | PubMed |
description | BACKGROUND: Elevated uric acid (UA) is commonly associated with gout and it is also a known cardiovascular disease risk factor. In contrast to such deleterious effects, UA possesses neuroprotective properties in the brain and elucidating the molecular mechanisms involved may have significant value regarding the therapeutic treatment of neurodegenerative disease. However, it is not yet fully established how UA levels are regulated in the brain. In this study, we investigated the distribution of mouse urate transporter 1 (URAT1) in the brain. URAT1 is a major reabsorptive urate transporter predominantly found in the kidney. METHODS: Immunohistochemistry of wild type and URAT1 knockout mouse brain using paraffin or frozen sections and a rabbit polyclonal anti-mouse URAT1 antibody were employed. RESULTS: Antibody specificity was confirmed by the lack of immunostaining in brain tissue from URAT1 knockout mice. URAT1 was distributed throughout the ventricular walls of the lateral ventricle, dorsal third ventricle, ventral third ventricle, aqueduct, and fourth ventricle, but not in the non-ciliated tanycytes in the lower part of the ventral third ventricle. URAT1 was localized to the apical membrane, including the cilia, of ependymal cells lining the wall of the ventricles that separates cerebrospinal fluid (CSF) and brain tissue. CONCLUSION: In this study, we report that URAT1 is expressed on cilia and the apical surface of ventricular ependymal cells. This is the first report to demonstrate expression of the urate transporter in ventricular ependymal cells and thus raises the possibility of a novel urate transport system involving CSF. |
format | Online Article Text |
id | pubmed-4015888 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40158882014-05-10 Ependymal cells of the mouse brain express urate transporter 1 (URAT1) Tomioka, Naoko H Nakamura, Makiko Doshi, Masaru Deguchi, Yoshiharu Ichida, Kimiyoshi Morisaki, Takayuki Hosoyamada, Makoto Fluids Barriers CNS Research BACKGROUND: Elevated uric acid (UA) is commonly associated with gout and it is also a known cardiovascular disease risk factor. In contrast to such deleterious effects, UA possesses neuroprotective properties in the brain and elucidating the molecular mechanisms involved may have significant value regarding the therapeutic treatment of neurodegenerative disease. However, it is not yet fully established how UA levels are regulated in the brain. In this study, we investigated the distribution of mouse urate transporter 1 (URAT1) in the brain. URAT1 is a major reabsorptive urate transporter predominantly found in the kidney. METHODS: Immunohistochemistry of wild type and URAT1 knockout mouse brain using paraffin or frozen sections and a rabbit polyclonal anti-mouse URAT1 antibody were employed. RESULTS: Antibody specificity was confirmed by the lack of immunostaining in brain tissue from URAT1 knockout mice. URAT1 was distributed throughout the ventricular walls of the lateral ventricle, dorsal third ventricle, ventral third ventricle, aqueduct, and fourth ventricle, but not in the non-ciliated tanycytes in the lower part of the ventral third ventricle. URAT1 was localized to the apical membrane, including the cilia, of ependymal cells lining the wall of the ventricles that separates cerebrospinal fluid (CSF) and brain tissue. CONCLUSION: In this study, we report that URAT1 is expressed on cilia and the apical surface of ventricular ependymal cells. This is the first report to demonstrate expression of the urate transporter in ventricular ependymal cells and thus raises the possibility of a novel urate transport system involving CSF. BioMed Central 2013-10-24 /pmc/articles/PMC4015888/ /pubmed/24156345 http://dx.doi.org/10.1186/2045-8118-10-31 Text en Copyright © 2013 Tomioka et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Tomioka, Naoko H Nakamura, Makiko Doshi, Masaru Deguchi, Yoshiharu Ichida, Kimiyoshi Morisaki, Takayuki Hosoyamada, Makoto Ependymal cells of the mouse brain express urate transporter 1 (URAT1) |
title | Ependymal cells of the mouse brain express urate transporter 1 (URAT1) |
title_full | Ependymal cells of the mouse brain express urate transporter 1 (URAT1) |
title_fullStr | Ependymal cells of the mouse brain express urate transporter 1 (URAT1) |
title_full_unstemmed | Ependymal cells of the mouse brain express urate transporter 1 (URAT1) |
title_short | Ependymal cells of the mouse brain express urate transporter 1 (URAT1) |
title_sort | ependymal cells of the mouse brain express urate transporter 1 (urat1) |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4015888/ https://www.ncbi.nlm.nih.gov/pubmed/24156345 http://dx.doi.org/10.1186/2045-8118-10-31 |
work_keys_str_mv | AT tomiokanaokoh ependymalcellsofthemousebrainexpressuratetransporter1urat1 AT nakamuramakiko ependymalcellsofthemousebrainexpressuratetransporter1urat1 AT doshimasaru ependymalcellsofthemousebrainexpressuratetransporter1urat1 AT deguchiyoshiharu ependymalcellsofthemousebrainexpressuratetransporter1urat1 AT ichidakimiyoshi ependymalcellsofthemousebrainexpressuratetransporter1urat1 AT morisakitakayuki ependymalcellsofthemousebrainexpressuratetransporter1urat1 AT hosoyamadamakoto ependymalcellsofthemousebrainexpressuratetransporter1urat1 |