TY - GEN
T1 - Microfluidic in vitro platforms of pulmonary alveolar physiology
AU - Tenenbaum-Katan, Janna
AU - Fishler, Rami
AU - Rothen-Rutishauser, Barbara
AU - Sznitman, Josué
N1 - Publisher Copyright: © Springer International Publishing Switzerland 2015.
PY - 2015
Y1 - 2015
N2 - Recreating realistic features of the pulmonary acinus within an experimental model system is among the great challenges of modern respiratory physiology. Intricate anatomical architecture, distinct physiological flow patterns and complex cellular functions all render limited experimental approaches, capturing only some aspects of acinar airway physiology. Microfluidic-based in vitro devices (μFIVDs) offer attractive advantages over conventional in vitro models, and thus miniaturized technologies are becoming more frequently implemented to recreate biomimetic models of the pulmonary tract. However, current μFIVDs still lack critical physiological aspects of the pulmonary acinus; models are often limited to single channels and operate under submerged conditions that are loosely reflecting the realistic acinar environment. Here, we present an anatomically-inspired and physiologically-relevant cell-based in vitro microfluidic platform that combines a multigeneration design of ductal airways and alveolar spaces and integrates confluent monolayers of alveolar epithelium, recreating either fluid-submerged or air-exposed environments. Our microfluidic platform provides robust tools to study numerous aspects of pulmonary physiology, including varying alveolar morphology during fetal development, the propagation of liquid plugs alog airways and cytotoxicity of airborne particles deposited on alveolar walls. Overall, we propose a versatile model that captures anatomical and physiological pulmonary functionalities while preserving homeostatic cellular microenvironments.
AB - Recreating realistic features of the pulmonary acinus within an experimental model system is among the great challenges of modern respiratory physiology. Intricate anatomical architecture, distinct physiological flow patterns and complex cellular functions all render limited experimental approaches, capturing only some aspects of acinar airway physiology. Microfluidic-based in vitro devices (μFIVDs) offer attractive advantages over conventional in vitro models, and thus miniaturized technologies are becoming more frequently implemented to recreate biomimetic models of the pulmonary tract. However, current μFIVDs still lack critical physiological aspects of the pulmonary acinus; models are often limited to single channels and operate under submerged conditions that are loosely reflecting the realistic acinar environment. Here, we present an anatomically-inspired and physiologically-relevant cell-based in vitro microfluidic platform that combines a multigeneration design of ductal airways and alveolar spaces and integrates confluent monolayers of alveolar epithelium, recreating either fluid-submerged or air-exposed environments. Our microfluidic platform provides robust tools to study numerous aspects of pulmonary physiology, including varying alveolar morphology during fetal development, the propagation of liquid plugs alog airways and cytotoxicity of airborne particles deposited on alveolar walls. Overall, we propose a versatile model that captures anatomical and physiological pulmonary functionalities while preserving homeostatic cellular microenvironments.
KW - Alveolar epithelium
KW - Microfluidic
KW - Pulmonary physiology
UR - http://www.scopus.com/inward/record.url?scp=84937793732&partnerID=8YFLogxK
U2 - https://doi.org/10.1007/978-3-319-11128-5_193
DO - https://doi.org/10.1007/978-3-319-11128-5_193
M3 - منشور من مؤتمر
T3 - IFMBE Proceedings
SP - 777
EP - 780
BT - 6th European Conference of the International Federation for Medical and Biological Engineering - MBEC 2014
A2 - Lackovic, Igor
A2 - Vasic, Darko
T2 - 6th European Conference of the International Federation for Medical and Biological Engineering, MBEC 2014
Y2 - 7 September 2014 through 11 September 2014
ER -