TY - JOUR
T1 - Localized electrical stimulation to C2C12 myotubes cultured on a porous membrane-based substrate
AU - Ishibashi, Takeshi
AU - Hoshino, Yu
AU - Kaji, Hirokazu
AU - Kanzaki, Makoto
AU - Sato, Masaaki
AU - Nishizawa, Matsuhiko
N1 - Funding Information:
Acknowledgement This study was supported by the Industrial Technology Research Grant Program from NEDO of Japan and by Grants-in-Aid for Scientific Research B (No. 20310070) from the Ministry of Education, Science, and Culture, Japan.
PY - 2009
Y1 - 2009
N2 - We report a porous membrane-based cell culture device that can conduct localized electrical stimulation of a cell monolayer. The device's cell culture substrate is a microporous alumina membrane with an underlying thin poly(dimethylsiloxane) (PDMS) film spotted with holes. When electric current is generated between the device's Pt ring electrodes-one of which is placed above the cells and the other below the PDMS layer-the current density condenses at the holes in the PDMS film, and cells located above the holes can be electrically stimulated. C2C12 cells were confluently cultured on the substrate and were differentiated to myotubes. To control the stimulated area in the substrate, we attempted to seal and reopen the holes of the PDMS film by using an air bubble. Since the current pulse could be effectively blocked at the sealed holes, fluorescent Ca2+ transients, indicative of cellular excitation, were observed from the myotubes located above holes in the open state.
AB - We report a porous membrane-based cell culture device that can conduct localized electrical stimulation of a cell monolayer. The device's cell culture substrate is a microporous alumina membrane with an underlying thin poly(dimethylsiloxane) (PDMS) film spotted with holes. When electric current is generated between the device's Pt ring electrodes-one of which is placed above the cells and the other below the PDMS layer-the current density condenses at the holes in the PDMS film, and cells located above the holes can be electrically stimulated. C2C12 cells were confluently cultured on the substrate and were differentiated to myotubes. To control the stimulated area in the substrate, we attempted to seal and reopen the holes of the PDMS film by using an air bubble. Since the current pulse could be effectively blocked at the sealed holes, fluorescent Ca2+ transients, indicative of cellular excitation, were observed from the myotubes located above holes in the open state.
KW - Bubble-sealing
KW - C2C12 myotube
KW - Catransient
KW - Electrical stimulation
KW - Porous alumina membrane
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U2 - 10.1007/s10544-008-9247-7
DO - 10.1007/s10544-008-9247-7
M3 - Article
C2 - 18975093
AN - SCOPUS:62649153318
SN - 1387-2176
VL - 11
SP - 413
EP - 419
JO - Biomedical Microdevices
JF - Biomedical Microdevices
IS - 2
ER -