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Cited 16 time in webofscience Cited 17 time in scopus
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Human Airway Primary Epithelial Cells Show Distinct Architectures on Membrane Supports Under Different Culture Conditionsopen access

Authors
Min, Kyoung AhRosania, Gus R.Shin, Meong Cheol
Issue Date
Jun-2016
Publisher
HUMANA PRESS INC
Keywords
Airway epithelial cell; NHBE; Porous membrane; Drug transport; Differentiation; Tight junction
Citation
CELL BIOCHEMISTRY AND BIOPHYSICS, v.74, no.2, pp 191 - 203
Pages
13
Indexed
SCIE
SCOPUS
Journal Title
CELL BIOCHEMISTRY AND BIOPHYSICS
Volume
74
Number
2
Start Page
191
End Page
203
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/15459
DOI
10.1007/s12013-016-0719-8
ISSN
1085-9195
1559-0283
Abstract
To facilitate drug development for lung delivery, it is highly demanding to establish appropriate airway epithelial cell models as transport barriers to evaluate pharmacokinetic profiles of drug molecules. Besides the cancer-derived cell lines, as the primary cell model, normal human bronchial epithelial (NHBE) cells have been used for drug screenings because of physiological relevance to in vivo. Therefore, to accurately interpret drug transport data in NHBE measured by different laboratories, it is important to know biophysical characteristics of NHBE grown on membranes in different culture conditions. In this study, NHBE was grown on the polyester membrane in a different medium and its transport barrier properties as well as cell architectures were fully characterized by functional assays and confocal imaging throughout the days of cultures. Moreover, NHBE cells on inserts in a different medium were subject to either of air-interfaced culture (AIC) or liquid-covered culture (LCC) condition. Cells in the AIC condition were cultivated on the membrane with medium in the basolateral side only, whereas cells with medium in apical and basolateral sides under the LCC condition. Quantitative microscopic imaging with biophysical examination revealed distinct multilayered architectures of differentiated NHBE cells, suggesting NHBE as functional cell barriers for the lung-targeting drug transport.
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