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Culture models to study leukocyte trafficking across the choroid plexus

BACKGROUND: A critical point during the course of central nervous system infection is the influx of leukocytes from the blood into the brain across the blood-brain barrier (BBB) and the blood-cerebrospinal fluid barrier (BCSFB). However, experimental in vitro models to investigate leukocyte transmig...

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Autores principales: Tenenbaum, Tobias, Steinmann, Ulrike, Friedrich, Corinna, Berger, Jürgen, Schwerk, Christian, Schroten, Horst
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3560101/
https://www.ncbi.nlm.nih.gov/pubmed/23305147
http://dx.doi.org/10.1186/2045-8118-10-1
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author Tenenbaum, Tobias
Steinmann, Ulrike
Friedrich, Corinna
Berger, Jürgen
Schwerk, Christian
Schroten, Horst
author_facet Tenenbaum, Tobias
Steinmann, Ulrike
Friedrich, Corinna
Berger, Jürgen
Schwerk, Christian
Schroten, Horst
author_sort Tenenbaum, Tobias
collection PubMed
description BACKGROUND: A critical point during the course of central nervous system infection is the influx of leukocytes from the blood into the brain across the blood-brain barrier (BBB) and the blood-cerebrospinal fluid barrier (BCSFB). However, experimental in vitro models to investigate leukocyte transmigration across cultured choroid plexus epithelial cells have been lacking so far. METHODS: We have developed a porcine and human “inverted” culture insert system that enables leukocyte transmigration specifically from the physiologically relevant basolateral side. The models use primary porcine choroid plexus epithelial cells (PCPEC) and human choroid plexus papilloma cells (HIBCPP). As a prerequisite for a functional barrier, we optimized culture conditions in which cells are maintained in serum-containing medium until high barrier function is reached. Leukocyte transmigration through the plexus epithelial cells is analysed by three-dimensional Apotome(®)-imaging and electron microscopy, and the route of transmigration through the plexus epithelial cells, i.e. transcellular as well as paracellular, can be determined. DISCUSSION: As a functionally relevant porcine and human BCSFB model, PCPEC and HIBCPP respectively, offer a wide range of options for analysis of disease-related mechanisms at the choroid plexus epithelium, especially involving human pathogens. Moreover, our in vitro models facilitate the investigation of leukocyte entry into the CNS via the blood-CSF barrier.
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spelling pubmed-35601012013-02-04 Culture models to study leukocyte trafficking across the choroid plexus Tenenbaum, Tobias Steinmann, Ulrike Friedrich, Corinna Berger, Jürgen Schwerk, Christian Schroten, Horst Fluids Barriers CNS Study Protocol BACKGROUND: A critical point during the course of central nervous system infection is the influx of leukocytes from the blood into the brain across the blood-brain barrier (BBB) and the blood-cerebrospinal fluid barrier (BCSFB). However, experimental in vitro models to investigate leukocyte transmigration across cultured choroid plexus epithelial cells have been lacking so far. METHODS: We have developed a porcine and human “inverted” culture insert system that enables leukocyte transmigration specifically from the physiologically relevant basolateral side. The models use primary porcine choroid plexus epithelial cells (PCPEC) and human choroid plexus papilloma cells (HIBCPP). As a prerequisite for a functional barrier, we optimized culture conditions in which cells are maintained in serum-containing medium until high barrier function is reached. Leukocyte transmigration through the plexus epithelial cells is analysed by three-dimensional Apotome(®)-imaging and electron microscopy, and the route of transmigration through the plexus epithelial cells, i.e. transcellular as well as paracellular, can be determined. DISCUSSION: As a functionally relevant porcine and human BCSFB model, PCPEC and HIBCPP respectively, offer a wide range of options for analysis of disease-related mechanisms at the choroid plexus epithelium, especially involving human pathogens. Moreover, our in vitro models facilitate the investigation of leukocyte entry into the CNS via the blood-CSF barrier. BioMed Central 2013-01-10 /pmc/articles/PMC3560101/ /pubmed/23305147 http://dx.doi.org/10.1186/2045-8118-10-1 Text en Copyright ©2013 Tenenbaum et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Study Protocol
Tenenbaum, Tobias
Steinmann, Ulrike
Friedrich, Corinna
Berger, Jürgen
Schwerk, Christian
Schroten, Horst
Culture models to study leukocyte trafficking across the choroid plexus
title Culture models to study leukocyte trafficking across the choroid plexus
title_full Culture models to study leukocyte trafficking across the choroid plexus
title_fullStr Culture models to study leukocyte trafficking across the choroid plexus
title_full_unstemmed Culture models to study leukocyte trafficking across the choroid plexus
title_short Culture models to study leukocyte trafficking across the choroid plexus
title_sort culture models to study leukocyte trafficking across the choroid plexus
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3560101/
https://www.ncbi.nlm.nih.gov/pubmed/23305147
http://dx.doi.org/10.1186/2045-8118-10-1
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