Towards a Chronic Obstructive Pulmonary Disease (COPD) 3D in vitro model: Optimization of stromal and epithelial compartments of a Lung-on-Chip Platform

Chronic obstructive pulmonary disease (COPD) is a respiratory airway condition that generates chronic inflammation and airflow limitation in the lungs. It is caused mainly by chronic exposure to harmful particles or smoke (like that of cigarettes) and genetic susceptibility. Several mechanisms like...

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Autores:
Fragozo Mesa, Valeria
Tipo de recurso:
Trabajo de grado de pregrado
Fecha de publicación:
2025
Institución:
Universidad de los Andes
Repositorio:
Séneca: repositorio Uniandes
Idioma:
eng
OAI Identifier:
oai:repositorio.uniandes.edu.co:1992/75471
Acceso en línea:
https://hdl.handle.net/1992/75471
Palabra clave:
Air-Liquid Interface
Chronic Obstructive Pulmonary Disease
Lung-on-Chip
in vitro Breathing
Organs-on-Chip
Small Airway
Ingeniería
Rights
embargoedAccess
License
Attribution-NonCommercial-NoDerivatives 4.0 International
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dc.title.eng.fl_str_mv Towards a Chronic Obstructive Pulmonary Disease (COPD) 3D in vitro model: Optimization of stromal and epithelial compartments of a Lung-on-Chip Platform
title Towards a Chronic Obstructive Pulmonary Disease (COPD) 3D in vitro model: Optimization of stromal and epithelial compartments of a Lung-on-Chip Platform
spellingShingle Towards a Chronic Obstructive Pulmonary Disease (COPD) 3D in vitro model: Optimization of stromal and epithelial compartments of a Lung-on-Chip Platform
Air-Liquid Interface
Chronic Obstructive Pulmonary Disease
Lung-on-Chip
in vitro Breathing
Organs-on-Chip
Small Airway
Ingeniería
title_short Towards a Chronic Obstructive Pulmonary Disease (COPD) 3D in vitro model: Optimization of stromal and epithelial compartments of a Lung-on-Chip Platform
title_full Towards a Chronic Obstructive Pulmonary Disease (COPD) 3D in vitro model: Optimization of stromal and epithelial compartments of a Lung-on-Chip Platform
title_fullStr Towards a Chronic Obstructive Pulmonary Disease (COPD) 3D in vitro model: Optimization of stromal and epithelial compartments of a Lung-on-Chip Platform
title_full_unstemmed Towards a Chronic Obstructive Pulmonary Disease (COPD) 3D in vitro model: Optimization of stromal and epithelial compartments of a Lung-on-Chip Platform
title_sort Towards a Chronic Obstructive Pulmonary Disease (COPD) 3D in vitro model: Optimization of stromal and epithelial compartments of a Lung-on-Chip Platform
dc.creator.fl_str_mv Fragozo Mesa, Valeria
dc.contributor.advisor.none.fl_str_mv Bigio Roitman, David
dc.contributor.author.none.fl_str_mv Fragozo Mesa, Valeria
dc.subject.keyword.eng.fl_str_mv Air-Liquid Interface
Chronic Obstructive Pulmonary Disease
Lung-on-Chip
in vitro Breathing
Organs-on-Chip
Small Airway
topic Air-Liquid Interface
Chronic Obstructive Pulmonary Disease
Lung-on-Chip
in vitro Breathing
Organs-on-Chip
Small Airway
Ingeniería
dc.subject.themes.none.fl_str_mv Ingeniería
description Chronic obstructive pulmonary disease (COPD) is a respiratory airway condition that generates chronic inflammation and airflow limitation in the lungs. It is caused mainly by chronic exposure to harmful particles or smoke (like that of cigarettes) and genetic susceptibility. Several mechanisms like inflammation, oxidative stress and an imbalance between proteases and antiproteases cause a cascade of events that lead to airway remodeling, among other pathological changes. Currently there is no cure for COPD, however, several therapies aim at ameliorating symptoms and slowing disease progression. Recently new tools to evaluate new therapeutical approaches have been developed including 2D in vitro studies, organs-on-chip (OOC) and animal models. However, 2D and animal models are not the best at mimicking human physiology. Additionally, OOCs are focused on the alveolar area of the lung, and most do not incorporate mechanisms to mimic the tidal respiration of the lungs. To account for this gap, this work aims to optimize a lung-on-chip model that accurately represents human small airways and incorporates relevant cell populations, tidal respiration and an air liquid interface(ALI). To do so, an OOC previously designed by BiomimX Srl. was implemented, and the culture conditions were optimized both in static and dynamic conditions. Platforms were analyzed through bright-field microscopy and immunofluorescence to determine cell viability, proliferation and phenotypic markers able to characterize the microtissues. In the case of the stromal compartment, Bronchial Smooth Muscle Cells (BSMCs) showed the most promise in high density monocultures cultured in SmGm-2 or Mixed media. On the other hand, for the epithelial compartment Normal Human Bronchial Epithelial (NHBEs) cells were successfully cultured with an optimized smart seeding technique in BEGM/PneumaCult ALI media. In conclusion, in this study substantial advances were made towards the development of a COPD LOC model, opening the door for new integral therapeutical strategies to be discovered and tested.
publishDate 2025
dc.date.accessioned.none.fl_str_mv 2025-01-17T22:05:24Z
dc.date.issued.none.fl_str_mv 2025-01-17
dc.date.accepted.none.fl_str_mv 2025-01-17
dc.date.available.none.fl_str_mv 2028-01-16
dc.type.none.fl_str_mv Trabajo de grado - Pregrado
dc.type.driver.none.fl_str_mv info:eu-repo/semantics/bachelorThesis
dc.type.version.none.fl_str_mv info:eu-repo/semantics/acceptedVersion
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dc.identifier.instname.none.fl_str_mv instname:Universidad de los Andes
dc.identifier.reponame.none.fl_str_mv reponame:Repositorio Institucional Séneca
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dc.language.iso.none.fl_str_mv eng
language eng
dc.rights.en.fl_str_mv Attribution-NonCommercial-NoDerivatives 4.0 International
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dc.format.extent.none.fl_str_mv 36 páginas
dc.format.mimetype.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidad de los Andes
dc.publisher.program.none.fl_str_mv Ingeniería Biomédica
dc.publisher.faculty.none.fl_str_mv Facultad de Ingeniería
dc.publisher.department.none.fl_str_mv Departamento de Ingeniería Biomédica
publisher.none.fl_str_mv Universidad de los Andes
institution Universidad de los Andes
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spelling Bigio Roitman, Davidvirtual::22187-1Fragozo Mesa, Valeria2025-01-17T22:05:24Z2028-01-162025-01-172025-01-17https://hdl.handle.net/1992/75471instname:Universidad de los Andesreponame:Repositorio Institucional Sénecarepourl:https://repositorio.uniandes.edu.co/Chronic obstructive pulmonary disease (COPD) is a respiratory airway condition that generates chronic inflammation and airflow limitation in the lungs. It is caused mainly by chronic exposure to harmful particles or smoke (like that of cigarettes) and genetic susceptibility. Several mechanisms like inflammation, oxidative stress and an imbalance between proteases and antiproteases cause a cascade of events that lead to airway remodeling, among other pathological changes. Currently there is no cure for COPD, however, several therapies aim at ameliorating symptoms and slowing disease progression. Recently new tools to evaluate new therapeutical approaches have been developed including 2D in vitro studies, organs-on-chip (OOC) and animal models. However, 2D and animal models are not the best at mimicking human physiology. Additionally, OOCs are focused on the alveolar area of the lung, and most do not incorporate mechanisms to mimic the tidal respiration of the lungs. To account for this gap, this work aims to optimize a lung-on-chip model that accurately represents human small airways and incorporates relevant cell populations, tidal respiration and an air liquid interface(ALI). To do so, an OOC previously designed by BiomimX Srl. was implemented, and the culture conditions were optimized both in static and dynamic conditions. Platforms were analyzed through bright-field microscopy and immunofluorescence to determine cell viability, proliferation and phenotypic markers able to characterize the microtissues. In the case of the stromal compartment, Bronchial Smooth Muscle Cells (BSMCs) showed the most promise in high density monocultures cultured in SmGm-2 or Mixed media. On the other hand, for the epithelial compartment Normal Human Bronchial Epithelial (NHBEs) cells were successfully cultured with an optimized smart seeding technique in BEGM/PneumaCult ALI media. 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