TY - JOUR
T1 - Viscosity-aided electromechanical poration of cells for transfecting molecules
AU - Huang, Wenjing
AU - Sakuma, Shinya
AU - Tottori, Naotomo
AU - Sugano, Shigeo S.
AU - Yamanishi, Yoko
N1 - Funding Information:
This work was supported by Core Research for Evolutional Science and Technology (CREST), founded by Japan Science and Technology Agency (JST) (JPMJCR19S6). We are grateful to Dr Hiroko Takahashi at Saitama University for providing Chlamydomonas materials and to Professor Yoshinori Sawae and Mr. Hironori Shinmori for their support in the measurements of sample viscosity.
Publisher Copyright:
© 2022 The Royal Society of Chemistry.
PY - 2022
Y1 - 2022
N2 - Cell poration technologies offer opportunities not only to understand the activities of biological molecules but also to investigate genetic manipulation possibilities. Unfortunately, transferring large molecules that can carry huge genomic information is challenging. Here, we demonstrate electromechanical poration using a core-shell-structured microbubble generator, consisting of a fine microelectrode covered with a dielectric material. By introducing a microcavity at its tip, we could concentrate the electrical field with the application of electric pulses and generate microbubbles for electromechanical stimulation of cells. Specifically, the technology enables transfection with molecules that are thousands of kDa even into osteoblasts and Chlamydomonas, which are generally considered to be difficult to inject. Notably, we found that the transfection efficiency can be enhanced by adjusting the viscosity of the cell suspension, which was presumably achieved by remodeling of the membrane cytoskeleton. The applicability of the approach to a variety of cell types opens up numerous emerging gene engineering applications.
AB - Cell poration technologies offer opportunities not only to understand the activities of biological molecules but also to investigate genetic manipulation possibilities. Unfortunately, transferring large molecules that can carry huge genomic information is challenging. Here, we demonstrate electromechanical poration using a core-shell-structured microbubble generator, consisting of a fine microelectrode covered with a dielectric material. By introducing a microcavity at its tip, we could concentrate the electrical field with the application of electric pulses and generate microbubbles for electromechanical stimulation of cells. Specifically, the technology enables transfection with molecules that are thousands of kDa even into osteoblasts and Chlamydomonas, which are generally considered to be difficult to inject. Notably, we found that the transfection efficiency can be enhanced by adjusting the viscosity of the cell suspension, which was presumably achieved by remodeling of the membrane cytoskeleton. The applicability of the approach to a variety of cell types opens up numerous emerging gene engineering applications.
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U2 - 10.1039/d2lc00628f
DO - 10.1039/d2lc00628f
M3 - Article
C2 - 36263697
AN - SCOPUS:85141741912
SN - 1473-0197
JO - Lab on a Chip - Miniaturisation for Chemistry and Biology
JF - Lab on a Chip - Miniaturisation for Chemistry and Biology
ER -