Organotypic brain slice cultures as a model to study angiogenesis of brain vessels

Brain vessels are the most important structures in the brain to deliver energy and substrates to neurons. Brain vessels are composed of a complex interaction between endothelial cells, pericytes and astrocytes, controlling the entry of substrates into the brain. Damage of brain vessels and vascular...

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Main Authors: Bianca eHutter-Schmid, Kathrin M Kniewallner, Christian eHumpel
Format: Article
Language:English
Published: Frontiers Media S.A. 2015-09-01
Series:Frontiers in Cell and Developmental Biology
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fcell.2015.00052/full
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spelling doaj-965b78fe8806433ab7e337505ccc39872020-11-25T00:59:00ZengFrontiers Media S.A.Frontiers in Cell and Developmental Biology2296-634X2015-09-01310.3389/fcell.2015.00052148740Organotypic brain slice cultures as a model to study angiogenesis of brain vesselsBianca eHutter-Schmid0Kathrin M Kniewallner1Christian eHumpel2Innsbruck Med. UniversityInnsbruck Med. UniversityInnsbruck Med. UniversityBrain vessels are the most important structures in the brain to deliver energy and substrates to neurons. Brain vessels are composed of a complex interaction between endothelial cells, pericytes and astrocytes, controlling the entry of substrates into the brain. Damage of brain vessels and vascular impairment are general pathologies observed in different neurodegenerative disorders including e.g. Alzheimer´s disease. In order to study remodeling of brain vessels, simple 3-dimensional in vitro systems need to be developed. Organotypic brain slices of mice provide a potent tool to explore angiogenic effects of brain vessels in a complex 3-dimensional structure. Here we show that organotypic brain slices can be cultured from 110 µm thick sections of postnatal and adult mice brains. The vessels are immunohistochemically stained for laminin and collagen IV. Co-stainings are an appropriate method to visualize interaction of brain endothelial cells with pericytes and astrocytes in these vessels. Different exogenous stimuli such as fibroblast growth factor-2 or vascular endothelial growth factor induce angiogenesis or re-growth, respectively. Hyperthermia or acidosis reduces the vessel density in organotypic slices. In conclusion, organotypic brain slices exhibit a strong vascular network which can be used to study remodeling and angiogenesis of brain vessels in a 3-dimensional in vitro system.http://journal.frontiersin.org/Journal/10.3389/fcell.2015.00052/fullAngiogenesisvascularpericyteVesselorganotypic slice
collection DOAJ
language English
format Article
sources DOAJ
author Bianca eHutter-Schmid
Kathrin M Kniewallner
Christian eHumpel
spellingShingle Bianca eHutter-Schmid
Kathrin M Kniewallner
Christian eHumpel
Organotypic brain slice cultures as a model to study angiogenesis of brain vessels
Frontiers in Cell and Developmental Biology
Angiogenesis
vascular
pericyte
Vessel
organotypic slice
author_facet Bianca eHutter-Schmid
Kathrin M Kniewallner
Christian eHumpel
author_sort Bianca eHutter-Schmid
title Organotypic brain slice cultures as a model to study angiogenesis of brain vessels
title_short Organotypic brain slice cultures as a model to study angiogenesis of brain vessels
title_full Organotypic brain slice cultures as a model to study angiogenesis of brain vessels
title_fullStr Organotypic brain slice cultures as a model to study angiogenesis of brain vessels
title_full_unstemmed Organotypic brain slice cultures as a model to study angiogenesis of brain vessels
title_sort organotypic brain slice cultures as a model to study angiogenesis of brain vessels
publisher Frontiers Media S.A.
series Frontiers in Cell and Developmental Biology
issn 2296-634X
publishDate 2015-09-01
description Brain vessels are the most important structures in the brain to deliver energy and substrates to neurons. Brain vessels are composed of a complex interaction between endothelial cells, pericytes and astrocytes, controlling the entry of substrates into the brain. Damage of brain vessels and vascular impairment are general pathologies observed in different neurodegenerative disorders including e.g. Alzheimer´s disease. In order to study remodeling of brain vessels, simple 3-dimensional in vitro systems need to be developed. Organotypic brain slices of mice provide a potent tool to explore angiogenic effects of brain vessels in a complex 3-dimensional structure. Here we show that organotypic brain slices can be cultured from 110 µm thick sections of postnatal and adult mice brains. The vessels are immunohistochemically stained for laminin and collagen IV. Co-stainings are an appropriate method to visualize interaction of brain endothelial cells with pericytes and astrocytes in these vessels. Different exogenous stimuli such as fibroblast growth factor-2 or vascular endothelial growth factor induce angiogenesis or re-growth, respectively. Hyperthermia or acidosis reduces the vessel density in organotypic slices. In conclusion, organotypic brain slices exhibit a strong vascular network which can be used to study remodeling and angiogenesis of brain vessels in a 3-dimensional in vitro system.
topic Angiogenesis
vascular
pericyte
Vessel
organotypic slice
url http://journal.frontiersin.org/Journal/10.3389/fcell.2015.00052/full
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