Disruption of astrocyte-vascular coupling and the blood-brain barrier by invading glioma cells
dc.contributor.author | Watkins, Stacey | en |
dc.contributor.author | Robel, Stefanie | en |
dc.contributor.author | Kimbrough, Ian F. | en |
dc.contributor.author | Roldan, Stephanie M. | en |
dc.contributor.author | Ellis-Davies, Graham | en |
dc.contributor.author | Sontheimer, Harald | en |
dc.date.accessioned | 2018-02-21T16:29:05Z | en |
dc.date.available | 2018-02-21T16:29:05Z | en |
dc.date.issued | 2014-06-01 | en |
dc.description.abstract | 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 preexisting 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<sup>2+</sup>-dependent release of K<sup+</sup>. These findings have important clinical implications regarding blood flow in the tumorassociated brain and the ability to locally deliver chemotherapeutic drugs in disease. | en |
dc.description.version | Published version | en |
dc.format.extent | 15 pages | en |
dc.format.mimetype | application/pdf | en |
dc.identifier.doi | https://doi.org/10.1038/ncomms5196 | en |
dc.identifier.issn | 2041-1723 | en |
dc.identifier.orcid | Robel, S [0000-0001-6716-3670] | en |
dc.identifier.orcid | Sontheimer, H [0000-0002-5843-9871] | en |
dc.identifier.uri | http://hdl.handle.net/10919/82229 | en |
dc.identifier.volume | 5 | en |
dc.language.iso | en | en |
dc.publisher | Nature Publishing Group | en |
dc.relation.uri | http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000338838700021&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=930d57c9ac61a043676db62af60056c1 | en |
dc.rights | In Copyright | en |
dc.rights.uri | http://rightsstatements.org/vocab/InC/1.0/ | en |
dc.subject | endothelial growth-factor | en |
dc.subject | central-nervous-system | en |
dc.subject | glioblastoma-multiforme | en |
dc.subject | functional hyperemia | en |
dc.subject | alzheimers-disease | en |
dc.subject | in-vivo | en |
dc.subject | angiogenesis | en |
dc.subject | tumors | en |
dc.subject | expression | en |
dc.subject | pericytes | en |
dc.title | Disruption of astrocyte-vascular coupling and the blood-brain barrier by invading glioma cells | en |
dc.title.serial | Nature Communications | en |
dc.type | Article - Refereed | en |
dc.type.dcmitype | Text | en |
dc.type.other | Article - Refereed | en |
dc.type.other | Journal | en |
pubs.organisational-group | /Virginia Tech | en |
pubs.organisational-group | /Virginia Tech/All T&R Faculty | en |
pubs.organisational-group | /Virginia Tech/Faculty of Health Sciences | en |
pubs.organisational-group | /Virginia Tech/Science | en |
pubs.organisational-group | /Virginia Tech/Science/COS T&R Faculty | en |
pubs.organisational-group | /Virginia Tech/Science/School of Neuroscience | en |
pubs.organisational-group | /Virginia Tech/University Research Institutes | en |
pubs.organisational-group | /Virginia Tech/University Research Institutes/Virginia Tech Carilion Research Institute | en |
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