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Reelin expression in brain endothelial cells: an electron microscopy study

BACKGROUND: Reelin expression and function have been extensively studied in the brain, although its expression has been also reported in other tissues including blood. This raises the possibility that reelin might be able to cross the blood-brain barrier, which could be functionally relevant. Up-to-...

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Autores principales: Perez-Costas, Emma, Fenton, Erin Y, Caruncho, Hector J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4374371/
https://www.ncbi.nlm.nih.gov/pubmed/25887698
http://dx.doi.org/10.1186/s12868-015-0156-4
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author Perez-Costas, Emma
Fenton, Erin Y
Caruncho, Hector J
author_facet Perez-Costas, Emma
Fenton, Erin Y
Caruncho, Hector J
author_sort Perez-Costas, Emma
collection PubMed
description BACKGROUND: Reelin expression and function have been extensively studied in the brain, although its expression has been also reported in other tissues including blood. This raises the possibility that reelin might be able to cross the blood-brain barrier, which could be functionally relevant. Up-to-date no studies have been conducted to assess if reelin is present in the blood-brain barrier, which is mainly constituted by tightly packed endothelial cells. In this report we assessed the expression of reelin in brain capillaries using immunocytochemistry and electron microscopy. RESULTS: At the light microscope, reelin immunolabeling appeared in specific endothelial cells in brain areas that presented abundant diffuse labeling for this protein (e.g., layer I of the cortex, or the stratum lacunosum moleculare of the hippocampus), while it was mostly absent from capillaries in other brain areas (e.g., deeper cortical layers, or the CA1 layer of the hippocampus). As expected, at the electron microscope reelin labeling was observed in neurons of the cortex, where most of the labeling was associated with the rough endoplasmic reticulum. Importantly, reelin was also observed in some endothelial cells located in small capillaries, which confirmed the findings obtained at the light microscope. In these cells, reelin labeling was located primarily in caveolae (i.e., vesicles of transcytosis), and associated with the plasma membrane of the luminal side of endothelial cells. In addition, some scarce labeling was observed in the nuclear membrane. CONCLUSIONS: The presence of reelin immunolabeling in brain endothelial cells, and particularly in caveolar vesicles within these cells, suggests that reelin and/or reelin peptides may be able to cross the blood-brain barrier, which could have important physiological, pathological, and therapeutic implications.
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spelling pubmed-43743712015-03-27 Reelin expression in brain endothelial cells: an electron microscopy study Perez-Costas, Emma Fenton, Erin Y Caruncho, Hector J BMC Neurosci Research Article BACKGROUND: Reelin expression and function have been extensively studied in the brain, although its expression has been also reported in other tissues including blood. This raises the possibility that reelin might be able to cross the blood-brain barrier, which could be functionally relevant. Up-to-date no studies have been conducted to assess if reelin is present in the blood-brain barrier, which is mainly constituted by tightly packed endothelial cells. In this report we assessed the expression of reelin in brain capillaries using immunocytochemistry and electron microscopy. RESULTS: At the light microscope, reelin immunolabeling appeared in specific endothelial cells in brain areas that presented abundant diffuse labeling for this protein (e.g., layer I of the cortex, or the stratum lacunosum moleculare of the hippocampus), while it was mostly absent from capillaries in other brain areas (e.g., deeper cortical layers, or the CA1 layer of the hippocampus). As expected, at the electron microscope reelin labeling was observed in neurons of the cortex, where most of the labeling was associated with the rough endoplasmic reticulum. Importantly, reelin was also observed in some endothelial cells located in small capillaries, which confirmed the findings obtained at the light microscope. In these cells, reelin labeling was located primarily in caveolae (i.e., vesicles of transcytosis), and associated with the plasma membrane of the luminal side of endothelial cells. In addition, some scarce labeling was observed in the nuclear membrane. CONCLUSIONS: The presence of reelin immunolabeling in brain endothelial cells, and particularly in caveolar vesicles within these cells, suggests that reelin and/or reelin peptides may be able to cross the blood-brain barrier, which could have important physiological, pathological, and therapeutic implications. BioMed Central 2015-03-24 /pmc/articles/PMC4374371/ /pubmed/25887698 http://dx.doi.org/10.1186/s12868-015-0156-4 Text en © Perez-Costas et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Perez-Costas, Emma
Fenton, Erin Y
Caruncho, Hector J
Reelin expression in brain endothelial cells: an electron microscopy study
title Reelin expression in brain endothelial cells: an electron microscopy study
title_full Reelin expression in brain endothelial cells: an electron microscopy study
title_fullStr Reelin expression in brain endothelial cells: an electron microscopy study
title_full_unstemmed Reelin expression in brain endothelial cells: an electron microscopy study
title_short Reelin expression in brain endothelial cells: an electron microscopy study
title_sort reelin expression in brain endothelial cells: an electron microscopy study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4374371/
https://www.ncbi.nlm.nih.gov/pubmed/25887698
http://dx.doi.org/10.1186/s12868-015-0156-4
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