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IVIVC Assessment of Two Mouse Brain Endothelial Cell Models for Drug Screening
Since most preclinical drug permeability assays across the blood-brain barrier (BBB) are still evaluated in rodents, we compared an in vitro mouse primary endothelial cell model to the mouse b.End3 and the acellular parallel artificial membrane permeability assay (PAMPA) models for drug screening pu...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6920823/ https://www.ncbi.nlm.nih.gov/pubmed/31717321 http://dx.doi.org/10.3390/pharmaceutics11110587 |
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author | Puscas, Ina Bernard-Patrzynski, Florian Jutras, Martin Lécuyer, Marc-André Bourbonnière, Lyne Prat, Alexandre Leclair, Grégoire Roullin, V. Gaëlle |
author_facet | Puscas, Ina Bernard-Patrzynski, Florian Jutras, Martin Lécuyer, Marc-André Bourbonnière, Lyne Prat, Alexandre Leclair, Grégoire Roullin, V. Gaëlle |
author_sort | Puscas, Ina |
collection | PubMed |
description | Since most preclinical drug permeability assays across the blood-brain barrier (BBB) are still evaluated in rodents, we compared an in vitro mouse primary endothelial cell model to the mouse b.End3 and the acellular parallel artificial membrane permeability assay (PAMPA) models for drug screening purposes. The mRNA expression of key feature membrane proteins of primary and bEnd.3 mouse brain endothelial cells were compared. Transwell(®) monolayer models were further characterized in terms of tightness and integrity. The in vitro in vivo correlation (IVIVC) was obtained by the correlation of the in vitro permeability data with log BB values obtained in mice for seven drugs. The mouse primary model showed higher monolayer integrity and levels of mRNA expression of BBB tight junction (TJ) proteins and membrane transporters (MBRT), especially for the efflux transporter Pgp. The IVIVC and drug ranking underlined the superiority of the primary model (r(2) = 0.765) when compared to the PAMPA-BBB (r(2) = 0.391) and bEnd.3 cell line (r(2) = 0.019) models. The primary monolayer mouse model came out as a simple and reliable candidate for the prediction of drug permeability across the BBB. This model encompasses a rapid set-up, a fair reproduction of BBB tissue characteristics, and an accurate drug screening. |
format | Online Article Text |
id | pubmed-6920823 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-69208232019-12-24 IVIVC Assessment of Two Mouse Brain Endothelial Cell Models for Drug Screening Puscas, Ina Bernard-Patrzynski, Florian Jutras, Martin Lécuyer, Marc-André Bourbonnière, Lyne Prat, Alexandre Leclair, Grégoire Roullin, V. Gaëlle Pharmaceutics Article Since most preclinical drug permeability assays across the blood-brain barrier (BBB) are still evaluated in rodents, we compared an in vitro mouse primary endothelial cell model to the mouse b.End3 and the acellular parallel artificial membrane permeability assay (PAMPA) models for drug screening purposes. The mRNA expression of key feature membrane proteins of primary and bEnd.3 mouse brain endothelial cells were compared. Transwell(®) monolayer models were further characterized in terms of tightness and integrity. The in vitro in vivo correlation (IVIVC) was obtained by the correlation of the in vitro permeability data with log BB values obtained in mice for seven drugs. The mouse primary model showed higher monolayer integrity and levels of mRNA expression of BBB tight junction (TJ) proteins and membrane transporters (MBRT), especially for the efflux transporter Pgp. The IVIVC and drug ranking underlined the superiority of the primary model (r(2) = 0.765) when compared to the PAMPA-BBB (r(2) = 0.391) and bEnd.3 cell line (r(2) = 0.019) models. The primary monolayer mouse model came out as a simple and reliable candidate for the prediction of drug permeability across the BBB. This model encompasses a rapid set-up, a fair reproduction of BBB tissue characteristics, and an accurate drug screening. MDPI 2019-11-08 /pmc/articles/PMC6920823/ /pubmed/31717321 http://dx.doi.org/10.3390/pharmaceutics11110587 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Puscas, Ina Bernard-Patrzynski, Florian Jutras, Martin Lécuyer, Marc-André Bourbonnière, Lyne Prat, Alexandre Leclair, Grégoire Roullin, V. Gaëlle IVIVC Assessment of Two Mouse Brain Endothelial Cell Models for Drug Screening |
title | IVIVC Assessment of Two Mouse Brain Endothelial Cell Models for Drug Screening |
title_full | IVIVC Assessment of Two Mouse Brain Endothelial Cell Models for Drug Screening |
title_fullStr | IVIVC Assessment of Two Mouse Brain Endothelial Cell Models for Drug Screening |
title_full_unstemmed | IVIVC Assessment of Two Mouse Brain Endothelial Cell Models for Drug Screening |
title_short | IVIVC Assessment of Two Mouse Brain Endothelial Cell Models for Drug Screening |
title_sort | ivivc assessment of two mouse brain endothelial cell models for drug screening |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6920823/ https://www.ncbi.nlm.nih.gov/pubmed/31717321 http://dx.doi.org/10.3390/pharmaceutics11110587 |
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