Novel three-dimensional biochip pulmonary sarcoidosis model.

Sarcoidosis is a multi-system disorder of granulomatous inflammation which most commonly affects the lungs. Its etiology and pathogenesis are not well defined in part due to the lack of reliable modeling. Here, we present the development of an in vitro three-dimensional lung-on-chip biochip designed...

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Main Authors: Tess M Calcagno, Chongxu Zhang, Runxia Tian, Babak Ebrahimi, Mehdi Mirsaeidi
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2021-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0245805
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spelling doaj-857d3e772597422a9060370f37b413432021-07-29T04:32:53ZengPublic Library of Science (PLoS)PLoS ONE1932-62032021-01-01162e024580510.1371/journal.pone.0245805Novel three-dimensional biochip pulmonary sarcoidosis model.Tess M CalcagnoChongxu ZhangRunxia TianBabak EbrahimiMehdi MirsaeidiSarcoidosis is a multi-system disorder of granulomatous inflammation which most commonly affects the lungs. Its etiology and pathogenesis are not well defined in part due to the lack of reliable modeling. Here, we present the development of an in vitro three-dimensional lung-on-chip biochip designed to mimic granuloma formation. A lung on chip fluidic macrodevice was developed and added to our previously developed a lung-on-membrane model (LOMM). Granulomas were cultured from blood samples of patients with sarcoidosis and then inserted in the air-lung-interface of the microchip to create a three-dimensional biochip pulmonary sarcoidosis model (3D BSGM). Cytokines were measured after 48 hours. ELISA testing was performed to measure cytokine response difference between LOMM with 3D BSGM. There were statistically significant differences in IL-1ß (P = 0.001953), IL-6 (P = 0.001953), GM-CSF (P = 0.001953), and INF-γ expressions (P = 0.09375) between two groups. The current model represents the first 3D biochip sarcoidosis model created by adding a microfluidics system to a dual-chambered lung on membrane model and introducing developed sarcoid-granuloma to its air-lung-interface.https://doi.org/10.1371/journal.pone.0245805
collection DOAJ
language English
format Article
sources DOAJ
author Tess M Calcagno
Chongxu Zhang
Runxia Tian
Babak Ebrahimi
Mehdi Mirsaeidi
spellingShingle Tess M Calcagno
Chongxu Zhang
Runxia Tian
Babak Ebrahimi
Mehdi Mirsaeidi
Novel three-dimensional biochip pulmonary sarcoidosis model.
PLoS ONE
author_facet Tess M Calcagno
Chongxu Zhang
Runxia Tian
Babak Ebrahimi
Mehdi Mirsaeidi
author_sort Tess M Calcagno
title Novel three-dimensional biochip pulmonary sarcoidosis model.
title_short Novel three-dimensional biochip pulmonary sarcoidosis model.
title_full Novel three-dimensional biochip pulmonary sarcoidosis model.
title_fullStr Novel three-dimensional biochip pulmonary sarcoidosis model.
title_full_unstemmed Novel three-dimensional biochip pulmonary sarcoidosis model.
title_sort novel three-dimensional biochip pulmonary sarcoidosis model.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2021-01-01
description Sarcoidosis is a multi-system disorder of granulomatous inflammation which most commonly affects the lungs. Its etiology and pathogenesis are not well defined in part due to the lack of reliable modeling. Here, we present the development of an in vitro three-dimensional lung-on-chip biochip designed to mimic granuloma formation. A lung on chip fluidic macrodevice was developed and added to our previously developed a lung-on-membrane model (LOMM). Granulomas were cultured from blood samples of patients with sarcoidosis and then inserted in the air-lung-interface of the microchip to create a three-dimensional biochip pulmonary sarcoidosis model (3D BSGM). Cytokines were measured after 48 hours. ELISA testing was performed to measure cytokine response difference between LOMM with 3D BSGM. There were statistically significant differences in IL-1ß (P = 0.001953), IL-6 (P = 0.001953), GM-CSF (P = 0.001953), and INF-γ expressions (P = 0.09375) between two groups. The current model represents the first 3D biochip sarcoidosis model created by adding a microfluidics system to a dual-chambered lung on membrane model and introducing developed sarcoid-granuloma to its air-lung-interface.
url https://doi.org/10.1371/journal.pone.0245805
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AT runxiatian novelthreedimensionalbiochippulmonarysarcoidosismodel
AT babakebrahimi novelthreedimensionalbiochippulmonarysarcoidosismodel
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