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2005 Volume No 10
pages 23-30
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Title:A noninvasive transfer system for polarized renal
tubule epithelial cell sheets using temperature-responsive
culture dishes
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Authors: A. Kushida, M. Yamato, Y. Isoi, A. Kikuchi,
T. Okano
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Address: Institute of Advanced Biomedical Engineering
and Science, Tokyo Womens Medical University, 8-1 Kawada-cho,
Shinjuku-ku, Tokyo 162-8666, Japan
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E-mail: tokano@abmes.twmu.ac.jp
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Key Words: Tissue engineering, poly(Nisopropylacrylamide),
tight junction, cell sheet engineering, confocal laser scanning
microscopy.
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Publication date: August 8th 2005
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Abstract: We used temperature-responsive culture
dishes onto which the temperature-responsive polymer, poly(Nisopropylacrylamide),
was covalently grafted for tissue
engineering. Confluent cells harvested as intact sheets from
these surfaces by simple temperature reduction can be transferred
to various surfaces including additional culture
dishes, other cell sheets, and tissues. In order to examine
the maintenance of cell polarity, Madin-Darby canine kidney
cells and human primary renal proximal tubule
epithelial cells which had developed apical-basal cell polarity
in culture, were subjected to cell sheet transfer. This functional
and structural cell polarity, which is susceptible to treatment
with trypsin, was examined by immunohistochemistry and transmission
electron
microscopy. Using our cell-sheet method, the noninvasive transfer
of these cell sheets retaining typical distributions of Na+/K+-ATPase,
GLUT-1, SGLT-1, aquaporin-1, neutral
endopeptidase and dipeptidylendopeptidase IV, could be achieved.
The transferred cell sheets also developed numerous microvilli
and tight junctions at the apical and lateral membranes, respectively.
For biochemical analysis, immunoblotting of occludin, a transmembrane
protein that composes tight junctions, was conducted and results
confirmed that occludin remained intact after cell sheet transfer.
This two-dimensional cell sheet manipulation method promises
to be useful for tissue engineering as well as in the investigation
of epithelial cell polarity.
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