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Characterization of ABC Transporters in EpiAirway™, a Cellular Model of Normal Human Bronchial Epithelium
The ATP-binding cassette (ABC) transporters P-glycoprotein (MDR1/ABCB1), multidrug resistance-associated protein 1 (MRP1/ABCC1), and breast cancer resistance protein (BCRP/ABCG2) play a crucial role in the translocation of a broad range of drugs; data about their expression and activity in lung tiss...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7247561/ https://www.ncbi.nlm.nih.gov/pubmed/32366035 http://dx.doi.org/10.3390/ijms21093190 |
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author | Rotoli, Bianca Maria Barilli, Amelia Visigalli, Rossana Ferrari, Francesca Frati, Caterina Lagrasta, Costanza Annamaria Di Lascia, Maria Riccardi, Benedetta Puccini, Paola Dall’Asta, Valeria |
author_facet | Rotoli, Bianca Maria Barilli, Amelia Visigalli, Rossana Ferrari, Francesca Frati, Caterina Lagrasta, Costanza Annamaria Di Lascia, Maria Riccardi, Benedetta Puccini, Paola Dall’Asta, Valeria |
author_sort | Rotoli, Bianca Maria |
collection | PubMed |
description | The ATP-binding cassette (ABC) transporters P-glycoprotein (MDR1/ABCB1), multidrug resistance-associated protein 1 (MRP1/ABCC1), and breast cancer resistance protein (BCRP/ABCG2) play a crucial role in the translocation of a broad range of drugs; data about their expression and activity in lung tissue are controversial. Here, we address their expression, localization and function in EpiAirway™, a three-dimensional (3D)-model of human airways; Calu-3 cells, a representative in vitro model of bronchial epithelium, are used for comparison. Transporter expression has been evaluated with RT-qPCR and Western blot, the localization with immunocytochemistry, and the activity by measuring the apical-to-basolateral and basolateral-to-apical fluxes of specific substrates in the presence of inhibitors. EpiAirway™ and Calu-3 cells express high levels of MRP1 on the basolateral membrane, while they profoundly differ in terms of BCRP and MDR1: BCRP is detected in EpiAirway™, but not in Calu-3 cells, while MDR1 is expressed and functional only in fully-differentiated Calu-3; in EpiAirway™, MDR1 expression and activity are undetectable, consistently with the absence of the protein in specimens from human healthy bronchi. In summary, EpiAirway™ appears to be a promising tool to study the mechanisms of drug delivery in the bronchial epithelium and to clarify the role of ABC transporters in the modulation of the bioavailability of administered drugs. |
format | Online Article Text |
id | pubmed-7247561 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-72475612020-06-10 Characterization of ABC Transporters in EpiAirway™, a Cellular Model of Normal Human Bronchial Epithelium Rotoli, Bianca Maria Barilli, Amelia Visigalli, Rossana Ferrari, Francesca Frati, Caterina Lagrasta, Costanza Annamaria Di Lascia, Maria Riccardi, Benedetta Puccini, Paola Dall’Asta, Valeria Int J Mol Sci Article The ATP-binding cassette (ABC) transporters P-glycoprotein (MDR1/ABCB1), multidrug resistance-associated protein 1 (MRP1/ABCC1), and breast cancer resistance protein (BCRP/ABCG2) play a crucial role in the translocation of a broad range of drugs; data about their expression and activity in lung tissue are controversial. Here, we address their expression, localization and function in EpiAirway™, a three-dimensional (3D)-model of human airways; Calu-3 cells, a representative in vitro model of bronchial epithelium, are used for comparison. Transporter expression has been evaluated with RT-qPCR and Western blot, the localization with immunocytochemistry, and the activity by measuring the apical-to-basolateral and basolateral-to-apical fluxes of specific substrates in the presence of inhibitors. EpiAirway™ and Calu-3 cells express high levels of MRP1 on the basolateral membrane, while they profoundly differ in terms of BCRP and MDR1: BCRP is detected in EpiAirway™, but not in Calu-3 cells, while MDR1 is expressed and functional only in fully-differentiated Calu-3; in EpiAirway™, MDR1 expression and activity are undetectable, consistently with the absence of the protein in specimens from human healthy bronchi. In summary, EpiAirway™ appears to be a promising tool to study the mechanisms of drug delivery in the bronchial epithelium and to clarify the role of ABC transporters in the modulation of the bioavailability of administered drugs. MDPI 2020-04-30 /pmc/articles/PMC7247561/ /pubmed/32366035 http://dx.doi.org/10.3390/ijms21093190 Text en © 2020 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 Rotoli, Bianca Maria Barilli, Amelia Visigalli, Rossana Ferrari, Francesca Frati, Caterina Lagrasta, Costanza Annamaria Di Lascia, Maria Riccardi, Benedetta Puccini, Paola Dall’Asta, Valeria Characterization of ABC Transporters in EpiAirway™, a Cellular Model of Normal Human Bronchial Epithelium |
title | Characterization of ABC Transporters in EpiAirway™, a Cellular Model of Normal Human Bronchial Epithelium |
title_full | Characterization of ABC Transporters in EpiAirway™, a Cellular Model of Normal Human Bronchial Epithelium |
title_fullStr | Characterization of ABC Transporters in EpiAirway™, a Cellular Model of Normal Human Bronchial Epithelium |
title_full_unstemmed | Characterization of ABC Transporters in EpiAirway™, a Cellular Model of Normal Human Bronchial Epithelium |
title_short | Characterization of ABC Transporters in EpiAirway™, a Cellular Model of Normal Human Bronchial Epithelium |
title_sort | characterization of abc transporters in epiairway™, a cellular model of normal human bronchial epithelium |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7247561/ https://www.ncbi.nlm.nih.gov/pubmed/32366035 http://dx.doi.org/10.3390/ijms21093190 |
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