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CB(1) cannabinoid receptor enrichment in the ependymal region of the adult human spinal cord
Cannabinoids are involved in the regulation of neural stem cell biology and their receptors are expressed in the neurogenic niches of adult rodents. In the spinal cord of rats and mice, neural stem cells can be found in the ependymal region, surrounding the central canal, but there is evidence that...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4669459/ https://www.ncbi.nlm.nih.gov/pubmed/26634814 http://dx.doi.org/10.1038/srep17745 |
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author | Paniagua-Torija, Beatriz Arevalo-Martin, Angel Ferrer, Isidro Molina-Holgado, Eduardo Garcia-Ovejero, Daniel |
author_facet | Paniagua-Torija, Beatriz Arevalo-Martin, Angel Ferrer, Isidro Molina-Holgado, Eduardo Garcia-Ovejero, Daniel |
author_sort | Paniagua-Torija, Beatriz |
collection | PubMed |
description | Cannabinoids are involved in the regulation of neural stem cell biology and their receptors are expressed in the neurogenic niches of adult rodents. In the spinal cord of rats and mice, neural stem cells can be found in the ependymal region, surrounding the central canal, but there is evidence that this region is largely different in adult humans: lacks a patent canal and presents perivascular pseudorosettes, typically found in low grade ependymomas. Using Laser Capture Microdissection, Taqman gene expression assays and immunohistochemistry, we have studied the expression of endocannabinoid system components (receptors and enzymes) at the human spinal cord ependymal region. We observe that ependymal region is enriched in CB(1) cannabinoid receptor, due to high CB(1) expression in GFAP+ astrocytic domains. However, in human spinal cord levels that retain central canal patency we found ependymal cells with high CB(1) expression, equivalent to the CB(1)(HIGH) cell subpopulation described in rodents. Our results support the existence of ependymal CB(1)(HIGH) cells across species, and may encourage further studies on this subpopulation, although only in cases when central canal is patent. In the adult human ependyma, which usually shows central canal absence, CB(1) may play a different role by modulating astrocyte functions. |
format | Online Article Text |
id | pubmed-4669459 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46694592015-12-09 CB(1) cannabinoid receptor enrichment in the ependymal region of the adult human spinal cord Paniagua-Torija, Beatriz Arevalo-Martin, Angel Ferrer, Isidro Molina-Holgado, Eduardo Garcia-Ovejero, Daniel Sci Rep Article Cannabinoids are involved in the regulation of neural stem cell biology and their receptors are expressed in the neurogenic niches of adult rodents. In the spinal cord of rats and mice, neural stem cells can be found in the ependymal region, surrounding the central canal, but there is evidence that this region is largely different in adult humans: lacks a patent canal and presents perivascular pseudorosettes, typically found in low grade ependymomas. Using Laser Capture Microdissection, Taqman gene expression assays and immunohistochemistry, we have studied the expression of endocannabinoid system components (receptors and enzymes) at the human spinal cord ependymal region. We observe that ependymal region is enriched in CB(1) cannabinoid receptor, due to high CB(1) expression in GFAP+ astrocytic domains. However, in human spinal cord levels that retain central canal patency we found ependymal cells with high CB(1) expression, equivalent to the CB(1)(HIGH) cell subpopulation described in rodents. Our results support the existence of ependymal CB(1)(HIGH) cells across species, and may encourage further studies on this subpopulation, although only in cases when central canal is patent. In the adult human ependyma, which usually shows central canal absence, CB(1) may play a different role by modulating astrocyte functions. Nature Publishing Group 2015-12-04 /pmc/articles/PMC4669459/ /pubmed/26634814 http://dx.doi.org/10.1038/srep17745 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Paniagua-Torija, Beatriz Arevalo-Martin, Angel Ferrer, Isidro Molina-Holgado, Eduardo Garcia-Ovejero, Daniel CB(1) cannabinoid receptor enrichment in the ependymal region of the adult human spinal cord |
title | CB(1) cannabinoid receptor enrichment in the ependymal region of the adult human spinal cord |
title_full | CB(1) cannabinoid receptor enrichment in the ependymal region of the adult human spinal cord |
title_fullStr | CB(1) cannabinoid receptor enrichment in the ependymal region of the adult human spinal cord |
title_full_unstemmed | CB(1) cannabinoid receptor enrichment in the ependymal region of the adult human spinal cord |
title_short | CB(1) cannabinoid receptor enrichment in the ependymal region of the adult human spinal cord |
title_sort | cb(1) cannabinoid receptor enrichment in the ependymal region of the adult human spinal cord |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4669459/ https://www.ncbi.nlm.nih.gov/pubmed/26634814 http://dx.doi.org/10.1038/srep17745 |
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