Cargando…

Disruption of astrocyte-vascular coupling and the blood-brain barrier by invading glioma cells

Astrocytic endfeet cover the entire cerebral vasculature and serve as exchange sites for ions, metabolites, and energy substrates from the blood to the brain. They maintain endothelial tight junctions that form the blood-brain barrier (BBB) and release vasoactive molecules that regulate vascular ton...

Descripción completa

Detalles Bibliográficos
Autores principales: Watkins, Stacey, Robel, Stefanie, Kimbrough, Ian F., Robert, Stephanie M., Ellis-Davies, Graham, Sontheimer, Harald
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4127490/
https://www.ncbi.nlm.nih.gov/pubmed/24943270
http://dx.doi.org/10.1038/ncomms5196
_version_ 1782330031224127488
author Watkins, Stacey
Robel, Stefanie
Kimbrough, Ian F.
Robert, Stephanie M.
Ellis-Davies, Graham
Sontheimer, Harald
author_facet Watkins, Stacey
Robel, Stefanie
Kimbrough, Ian F.
Robert, Stephanie M.
Ellis-Davies, Graham
Sontheimer, Harald
author_sort Watkins, Stacey
collection PubMed
description Astrocytic endfeet cover the entire cerebral vasculature and serve as exchange sites for ions, metabolites, and energy substrates from the blood to the brain. They maintain endothelial tight junctions that form the blood-brain barrier (BBB) and release vasoactive molecules that regulate vascular tone. Malignant gliomas are highly invasive tumors that use the perivascular space for invasion and co-opt existing vessels as satellite tumors form. Here we use a clinically relevant mouse model of glioma and find that glioma cells, as they populate the perivascular space of pre-existing vessels, displace astrocytic endfeet from endothelial or vascular smooth muscle cells. This causes a focal breach in the BBB. Furthermore, astrocyte-mediated gliovascular coupling is lost, and glioma cells seize control over regulation of vascular tone through Ca(2+)-dependent release of K(+). These findings have important clinical implications regarding blood flow in the tumor-associated brain and the ability to locally deliver chemotherapeutic drugs in disease.
format Online
Article
Text
id pubmed-4127490
institution National Center for Biotechnology Information
language English
publishDate 2014
record_format MEDLINE/PubMed
spelling pubmed-41274902014-12-19 Disruption of astrocyte-vascular coupling and the blood-brain barrier by invading glioma cells Watkins, Stacey Robel, Stefanie Kimbrough, Ian F. Robert, Stephanie M. Ellis-Davies, Graham Sontheimer, Harald Nat Commun Article Astrocytic endfeet cover the entire cerebral vasculature and serve as exchange sites for ions, metabolites, and energy substrates from the blood to the brain. They maintain endothelial tight junctions that form the blood-brain barrier (BBB) and release vasoactive molecules that regulate vascular tone. Malignant gliomas are highly invasive tumors that use the perivascular space for invasion and co-opt existing vessels as satellite tumors form. Here we use a clinically relevant mouse model of glioma and find that glioma cells, as they populate the perivascular space of pre-existing vessels, displace astrocytic endfeet from endothelial or vascular smooth muscle cells. This causes a focal breach in the BBB. Furthermore, astrocyte-mediated gliovascular coupling is lost, and glioma cells seize control over regulation of vascular tone through Ca(2+)-dependent release of K(+). These findings have important clinical implications regarding blood flow in the tumor-associated brain and the ability to locally deliver chemotherapeutic drugs in disease. 2014-06-19 /pmc/articles/PMC4127490/ /pubmed/24943270 http://dx.doi.org/10.1038/ncomms5196 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Watkins, Stacey
Robel, Stefanie
Kimbrough, Ian F.
Robert, Stephanie M.
Ellis-Davies, Graham
Sontheimer, Harald
Disruption of astrocyte-vascular coupling and the blood-brain barrier by invading glioma cells
title Disruption of astrocyte-vascular coupling and the blood-brain barrier by invading glioma cells
title_full Disruption of astrocyte-vascular coupling and the blood-brain barrier by invading glioma cells
title_fullStr Disruption of astrocyte-vascular coupling and the blood-brain barrier by invading glioma cells
title_full_unstemmed Disruption of astrocyte-vascular coupling and the blood-brain barrier by invading glioma cells
title_short Disruption of astrocyte-vascular coupling and the blood-brain barrier by invading glioma cells
title_sort disruption of astrocyte-vascular coupling and the blood-brain barrier by invading glioma cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4127490/
https://www.ncbi.nlm.nih.gov/pubmed/24943270
http://dx.doi.org/10.1038/ncomms5196
work_keys_str_mv AT watkinsstacey disruptionofastrocytevascularcouplingandthebloodbrainbarrierbyinvadinggliomacells
AT robelstefanie disruptionofastrocytevascularcouplingandthebloodbrainbarrierbyinvadinggliomacells
AT kimbroughianf disruptionofastrocytevascularcouplingandthebloodbrainbarrierbyinvadinggliomacells
AT robertstephaniem disruptionofastrocytevascularcouplingandthebloodbrainbarrierbyinvadinggliomacells
AT ellisdaviesgraham disruptionofastrocytevascularcouplingandthebloodbrainbarrierbyinvadinggliomacells
AT sontheimerharald disruptionofastrocytevascularcouplingandthebloodbrainbarrierbyinvadinggliomacells