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A 3D Human Lung Tissue Model for Functional Studies on Mycobacterium tuberculosis Infection

Tuberculosis (TB) still holds a major threat to the health of people worldwide, and there is a need for cost-efficient but reliable models to help us understand the disease mechanisms and advance the discoveries of new treatment options. In vitro cell cultures of monolayers or co-cultures lack the t...

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Autores principales: Braian, Clara, Svensson, Mattias, Brighenti, Susanna, Lerm, Maria, Parasa, Venkata R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MyJove Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4692636/
https://www.ncbi.nlm.nih.gov/pubmed/26485646
http://dx.doi.org/10.3791/53084
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author Braian, Clara
Svensson, Mattias
Brighenti, Susanna
Lerm, Maria
Parasa, Venkata R.
author_facet Braian, Clara
Svensson, Mattias
Brighenti, Susanna
Lerm, Maria
Parasa, Venkata R.
author_sort Braian, Clara
collection PubMed
description Tuberculosis (TB) still holds a major threat to the health of people worldwide, and there is a need for cost-efficient but reliable models to help us understand the disease mechanisms and advance the discoveries of new treatment options. In vitro cell cultures of monolayers or co-cultures lack the three-dimensional (3D) environment and tissue responses. Herein, we describe an innovative in vitro model of a human lung tissue, which holds promise to be an effective tool for studying the complex events that occur during infection with Mycobacterium tuberculosis (M. tuberculosis). The 3D tissue model consists of tissue-specific epithelial cells and fibroblasts, which are cultured in a matrix of collagen on top of a porous membrane. Upon air exposure, the epithelial cells stratify and secrete mucus at the apical side. By introducing human primary macrophages infected with M. tuberculosis to the tissue model, we have shown that immune cells migrate into the infected-tissue and form early stages of TB granuloma. These structures recapitulate the distinct feature of human TB, the granuloma, which is fundamentally different or not commonly observed in widely used experimental animal models. This organotypic culture method enables the 3D visualization and robust quantitative analysis that provides pivotal information on spatial and temporal features of host cell-pathogen interactions. Taken together, the lung tissue model provides a physiologically relevant tissue micro-environment for studies on TB. Thus, the lung tissue model has potential implications for both basic mechanistic and applied studies. Importantly, the model allows addition or manipulation of individual cell types, which thereby widens its use for modelling a variety of infectious diseases that affect the lungs.
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spelling pubmed-46926362017-10-05 A 3D Human Lung Tissue Model for Functional Studies on Mycobacterium tuberculosis Infection Braian, Clara Svensson, Mattias Brighenti, Susanna Lerm, Maria Parasa, Venkata R. J Vis Exp Infection Tuberculosis (TB) still holds a major threat to the health of people worldwide, and there is a need for cost-efficient but reliable models to help us understand the disease mechanisms and advance the discoveries of new treatment options. In vitro cell cultures of monolayers or co-cultures lack the three-dimensional (3D) environment and tissue responses. Herein, we describe an innovative in vitro model of a human lung tissue, which holds promise to be an effective tool for studying the complex events that occur during infection with Mycobacterium tuberculosis (M. tuberculosis). The 3D tissue model consists of tissue-specific epithelial cells and fibroblasts, which are cultured in a matrix of collagen on top of a porous membrane. Upon air exposure, the epithelial cells stratify and secrete mucus at the apical side. By introducing human primary macrophages infected with M. tuberculosis to the tissue model, we have shown that immune cells migrate into the infected-tissue and form early stages of TB granuloma. These structures recapitulate the distinct feature of human TB, the granuloma, which is fundamentally different or not commonly observed in widely used experimental animal models. This organotypic culture method enables the 3D visualization and robust quantitative analysis that provides pivotal information on spatial and temporal features of host cell-pathogen interactions. Taken together, the lung tissue model provides a physiologically relevant tissue micro-environment for studies on TB. Thus, the lung tissue model has potential implications for both basic mechanistic and applied studies. Importantly, the model allows addition or manipulation of individual cell types, which thereby widens its use for modelling a variety of infectious diseases that affect the lungs. MyJove Corporation 2015-10-05 /pmc/articles/PMC4692636/ /pubmed/26485646 http://dx.doi.org/10.3791/53084 Text en Copyright © 2015, Journal of Visualized Experiments http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visithttp://creativecommons.org/licenses/by-nc-nd/3.0/
spellingShingle Infection
Braian, Clara
Svensson, Mattias
Brighenti, Susanna
Lerm, Maria
Parasa, Venkata R.
A 3D Human Lung Tissue Model for Functional Studies on Mycobacterium tuberculosis Infection
title A 3D Human Lung Tissue Model for Functional Studies on Mycobacterium tuberculosis Infection
title_full A 3D Human Lung Tissue Model for Functional Studies on Mycobacterium tuberculosis Infection
title_fullStr A 3D Human Lung Tissue Model for Functional Studies on Mycobacterium tuberculosis Infection
title_full_unstemmed A 3D Human Lung Tissue Model for Functional Studies on Mycobacterium tuberculosis Infection
title_short A 3D Human Lung Tissue Model for Functional Studies on Mycobacterium tuberculosis Infection
title_sort 3d human lung tissue model for functional studies on mycobacterium tuberculosis infection
topic Infection
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4692636/
https://www.ncbi.nlm.nih.gov/pubmed/26485646
http://dx.doi.org/10.3791/53084
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