TY - JOUR
T1 - Design of biomimetic substrates for long-term maintenance of alveolar epithelial cells
AU - Poon, James C.H.
AU - Liao, Zhongfa
AU - Suzuki, Takaya
AU - Carleton, Miranda M.
AU - Soleas, John P.
AU - Aitchison, J. Stewart
AU - Karoubi, Golnaz
AU - McGuigan, Alison P.
AU - Waddell, Thomas K.
N1 - Funding Information:
The authors would like to thank the Advanced Optical Microscopy Facility for access to confocal microscopy. This work was funded by a New Ideas Grant from the Canada First Research Excellence Fund – Medicine by Design Program to TKW and AM, a NSERC PGS D to JP, and a McGlaughlin Foundation grant and the Training Program in Organ-on-a-Chip Engineering & Entrepreneurship to JS.
Publisher Copyright:
© 2018 The Royal Society of Chemistry.
PY - 2018/2
Y1 - 2018/2
N2 - There is a need to establish in vitro lung alveolar epithelial culture models to better understand the fundamental biological mechanisms that drive lung diseases. While primary alveolar epithelial cells (AEC) are a useful option to study mature lung biology, they have limited utility in vitro. Cells that survive demonstrate limited proliferative capacity and loss of phenotype over the first 3-5 days in traditional culture conditions. To address this limitation, we generated a novel physiologically relevant cell culture system for enhanced viability and maintenance of phenotype. Here we describe a method utilizing e-beam lithography, reactive ion etching, and replica molding to generate poly-dimethylsiloxane (PDMS) substrates containing hemispherical cavities that mimic the architecture and size of mouse and human alveoli. Primary AECs grown on these cavity-containing substrates form a monolayer that conforms to the substrate enabling precise control over cell sheet architecture. AECs grown in cavity culture conditions remain viable and maintain their phenotype over one week. Specifically, cells grown on substrates consisting of 50 μm diameter cavities remained 96 ± 4% viable and maintained expression of surfactant protein C (SPC), a marker of type 2 AEC over 7 days. While this report focuses on primary lung alveolar epithelial cells, our culture platform is potentially relevant and useful for growing primary cells from other tissues with similar cavity-like architecture and could be further adapted to other biomimetic shapes or contours.
AB - There is a need to establish in vitro lung alveolar epithelial culture models to better understand the fundamental biological mechanisms that drive lung diseases. While primary alveolar epithelial cells (AEC) are a useful option to study mature lung biology, they have limited utility in vitro. Cells that survive demonstrate limited proliferative capacity and loss of phenotype over the first 3-5 days in traditional culture conditions. To address this limitation, we generated a novel physiologically relevant cell culture system for enhanced viability and maintenance of phenotype. Here we describe a method utilizing e-beam lithography, reactive ion etching, and replica molding to generate poly-dimethylsiloxane (PDMS) substrates containing hemispherical cavities that mimic the architecture and size of mouse and human alveoli. Primary AECs grown on these cavity-containing substrates form a monolayer that conforms to the substrate enabling precise control over cell sheet architecture. AECs grown in cavity culture conditions remain viable and maintain their phenotype over one week. Specifically, cells grown on substrates consisting of 50 μm diameter cavities remained 96 ± 4% viable and maintained expression of surfactant protein C (SPC), a marker of type 2 AEC over 7 days. While this report focuses on primary lung alveolar epithelial cells, our culture platform is potentially relevant and useful for growing primary cells from other tissues with similar cavity-like architecture and could be further adapted to other biomimetic shapes or contours.
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U2 - 10.1039/c7bm00647k
DO - 10.1039/c7bm00647k
M3 - Article
C2 - 29327014
AN - SCOPUS:85041332252
VL - 6
SP - 292
EP - 303
JO - Biomaterials Science
JF - Biomaterials Science
SN - 2047-4830
IS - 2
ER -