Ishibashi Takeshi, Hoshino Yu, Kaji Hirokazu, Kanzaki Makoto, Sato Masaaki, Nishizawa Matsuhiko
Department of Bioengineering and Robotics, Graduate School of Engineering, Tohoku University, 6-6-01 Aramaki, Aoba-ku, Sendai 980-8579, Japan.
Biomed Microdevices. 2009 Apr;11(2):413-9. doi: 10.1007/s10544-008-9247-7.
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.
我们报道了一种基于多孔膜的细胞培养装置,该装置可对细胞单层进行局部电刺激。该装置的细胞培养底物是一种微孔氧化铝膜,其下方有一层薄的聚二甲基硅氧烷(PDMS)膜,上面有许多小孔。当在该装置的铂环电极之间产生电流时(其中一个电极置于细胞上方,另一个置于PDMS层下方),电流密度会在PDMS膜的小孔处聚集,位于小孔上方的细胞就会受到电刺激。将C2C12细胞在该底物上进行汇合培养,并分化为肌管。为了控制底物中的刺激区域,我们尝试用气泡密封并重新打开PDMS膜的小孔。由于在密封的小孔处电流脉冲可被有效阻断,因此从处于开放状态的小孔上方的肌管中观察到了指示细胞兴奋的荧光Ca2+瞬变。