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Cannabinoid Type 1 Receptor is Undetectable in Rodent and Primate Cerebral Neural Stem Cells but Participates in Radial Neuronal Migration
Cannabinoid type 1 receptor (CB(1)R) is expressed and participates in several aspects of cerebral cortex embryonic development as demonstrated with whole-transcriptome mRNA sequencing and other contemporary methods. However, the cellular location of CB(1)R, which helps to specify molecular mechanism...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7696736/ https://www.ncbi.nlm.nih.gov/pubmed/33212822 http://dx.doi.org/10.3390/ijms21228657 |
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author | Morozov, Yury M. Mackie, Ken Rakic, Pasko |
author_facet | Morozov, Yury M. Mackie, Ken Rakic, Pasko |
author_sort | Morozov, Yury M. |
collection | PubMed |
description | Cannabinoid type 1 receptor (CB(1)R) is expressed and participates in several aspects of cerebral cortex embryonic development as demonstrated with whole-transcriptome mRNA sequencing and other contemporary methods. However, the cellular location of CB(1)R, which helps to specify molecular mechanisms, remains to be documented. Using three-dimensional (3D) electron microscopic reconstruction, we examined CB(1)R immunolabeling in proliferating neural stem cells (NSCs) and migrating neurons in the embryonic mouse (Mus musculus) and rhesus macaque (Macaca mulatta) cerebral cortex. We found that the mitotic and postmitotic ventricular and subventricular zone (VZ and SVZ) cells are immunonegative in both species while radially migrating neurons in the intermediate zone (IZ) and cortical plate (CP) contain CB(1)R-positive intracellular vesicles. CB(1)R immunolabeling was more numerous and more extensive in monkeys compared to mice. In CB(1)R-knock out mice, projection neurons in the IZ show migration abnormalities such as an increased number of lateral processes. Thus, in radially migrating neurons CB(1)R provides a molecular substrate for the regulation of cell movement. Undetectable level of CB(1)R in VZ/SVZ cells indicates that previously suggested direct CB(1)R-transmitted regulation of cellular proliferation and fate determination demands rigorous re-examination. More abundant CB(1)R expression in monkey compared to mouse suggests that therapeutic or recreational cannabis use may be more distressing for immature primate neurons than inferred from experiments with rodents. |
format | Online Article Text |
id | pubmed-7696736 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-76967362020-11-29 Cannabinoid Type 1 Receptor is Undetectable in Rodent and Primate Cerebral Neural Stem Cells but Participates in Radial Neuronal Migration Morozov, Yury M. Mackie, Ken Rakic, Pasko Int J Mol Sci Article Cannabinoid type 1 receptor (CB(1)R) is expressed and participates in several aspects of cerebral cortex embryonic development as demonstrated with whole-transcriptome mRNA sequencing and other contemporary methods. However, the cellular location of CB(1)R, which helps to specify molecular mechanisms, remains to be documented. Using three-dimensional (3D) electron microscopic reconstruction, we examined CB(1)R immunolabeling in proliferating neural stem cells (NSCs) and migrating neurons in the embryonic mouse (Mus musculus) and rhesus macaque (Macaca mulatta) cerebral cortex. We found that the mitotic and postmitotic ventricular and subventricular zone (VZ and SVZ) cells are immunonegative in both species while radially migrating neurons in the intermediate zone (IZ) and cortical plate (CP) contain CB(1)R-positive intracellular vesicles. CB(1)R immunolabeling was more numerous and more extensive in monkeys compared to mice. In CB(1)R-knock out mice, projection neurons in the IZ show migration abnormalities such as an increased number of lateral processes. Thus, in radially migrating neurons CB(1)R provides a molecular substrate for the regulation of cell movement. Undetectable level of CB(1)R in VZ/SVZ cells indicates that previously suggested direct CB(1)R-transmitted regulation of cellular proliferation and fate determination demands rigorous re-examination. More abundant CB(1)R expression in monkey compared to mouse suggests that therapeutic or recreational cannabis use may be more distressing for immature primate neurons than inferred from experiments with rodents. MDPI 2020-11-17 /pmc/articles/PMC7696736/ /pubmed/33212822 http://dx.doi.org/10.3390/ijms21228657 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Morozov, Yury M. Mackie, Ken Rakic, Pasko Cannabinoid Type 1 Receptor is Undetectable in Rodent and Primate Cerebral Neural Stem Cells but Participates in Radial Neuronal Migration |
title | Cannabinoid Type 1 Receptor is Undetectable in Rodent and Primate Cerebral Neural Stem Cells but Participates in Radial Neuronal Migration |
title_full | Cannabinoid Type 1 Receptor is Undetectable in Rodent and Primate Cerebral Neural Stem Cells but Participates in Radial Neuronal Migration |
title_fullStr | Cannabinoid Type 1 Receptor is Undetectable in Rodent and Primate Cerebral Neural Stem Cells but Participates in Radial Neuronal Migration |
title_full_unstemmed | Cannabinoid Type 1 Receptor is Undetectable in Rodent and Primate Cerebral Neural Stem Cells but Participates in Radial Neuronal Migration |
title_short | Cannabinoid Type 1 Receptor is Undetectable in Rodent and Primate Cerebral Neural Stem Cells but Participates in Radial Neuronal Migration |
title_sort | cannabinoid type 1 receptor is undetectable in rodent and primate cerebral neural stem cells but participates in radial neuronal migration |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7696736/ https://www.ncbi.nlm.nih.gov/pubmed/33212822 http://dx.doi.org/10.3390/ijms21228657 |
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