TY - JOUR
T1 - A practical device for pinpoint delivery of molecules into multiple neurons in culture
AU - Hara, Chikako
AU - Tateyama, Kiyohiko
AU - Akamatsu, Naoki
AU - Imabayashi, Hiroyuki
AU - Karaki, Koichi
AU - Nomura, Nobuo
AU - Okano, Hideyuki
AU - Miyawaki, Atsushi
N1 - Funding Information:
This work was partly supported by grants from a Japan MEXT Grant-in-Aid for Scientific Research on priority areas, NEDO (the New Energy and Industrial Technology Development Organization), HFSP (the Human Frontier Science Program), and the Japan Society for the Promotion of Science for Young Scientists. The authors thank Drs. Chitoshi Itakura and Yuichi Watanabe at BSI Olympus Collaboration Center for technical support.
PY - 2006/12
Y1 - 2006/12
N2 - We have developed a device for pinpoint delivery of chemicals, proteins, and nucleic acids into cultured cells. The principle underlying the technique is the flow of molecules from the culture medium into cells through a rupture in the plasma membrane made by a needle puncture. DNA transfection is achieved by stabbing the needle tip into the nucleus. The CellBee device can be attached to any inverted microscope, and molecular delivery can be coupled with conventional live cell imaging. Because the position of the needle relative to the targeted cultured cells is computer-controlled, efficient delivery of molecules such as rhodamine into as many as 100 HeLa cells can be completed in 10 min. Moreover, specific target cells within a single dish can be transfected with multiple DNA constructs by simple changes of culture medium containing different plasmids. In addition, the nano-sized needle tip enables gentle molecular delivery, minimizing cell damage. This method permits DNA transfection into specific hippocampal neurons without disturbing neuronal circuitry established in culture.
AB - We have developed a device for pinpoint delivery of chemicals, proteins, and nucleic acids into cultured cells. The principle underlying the technique is the flow of molecules from the culture medium into cells through a rupture in the plasma membrane made by a needle puncture. DNA transfection is achieved by stabbing the needle tip into the nucleus. The CellBee device can be attached to any inverted microscope, and molecular delivery can be coupled with conventional live cell imaging. Because the position of the needle relative to the targeted cultured cells is computer-controlled, efficient delivery of molecules such as rhodamine into as many as 100 HeLa cells can be completed in 10 min. Moreover, specific target cells within a single dish can be transfected with multiple DNA constructs by simple changes of culture medium containing different plasmids. In addition, the nano-sized needle tip enables gentle molecular delivery, minimizing cell damage. This method permits DNA transfection into specific hippocampal neurons without disturbing neuronal circuitry established in culture.
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U2 - 10.1007/s11068-008-9021-z
DO - 10.1007/s11068-008-9021-z
M3 - Article
C2 - 18392728
AN - SCOPUS:44149092367
SN - 1559-7105
VL - 35
SP - 229
EP - 237
JO - Brain Cell Biology
JF - Brain Cell Biology
IS - 4-6
ER -