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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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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