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Merck

Dielectrophoresis-assisted 3D nanoelectroporation for non-viral cell transfection in adoptive immunotherapy.

Lab on a chip (2015-06-25)
Lingqian Chang, Daniel Gallego-Perez, Xi Zhao, Paul Bertani, Zhaogang Yang, Chi-Ling Chiang, Veysi Malkoc, Junfeng Shi, Chandan K Sen, Lynn Odonnell, Jianhua Yu, Wu Lu, L James Lee
RESUMEN

Current transfection technologies lead to significant inter-clonal variations. Previously we introduced a unique electrotransfection technology, Nanochannel-Electroporation (NEP), which can precisely and benignly transfect small cell populations (~100-200 cells) with single-cell resolution. Here we report on the development of a novel 3D NEP system for large scale transfection. A properly-engineered array of nanochannels, capable of handling/transfecting ~60 000 cells cm(-2), was fabricated using cleanroom technologies. Positive dielectrophoresis was used to selectively position cells on the nanochannels, thus allowing highly efficient transfection. Single-cell dosage control was demonstrated using both small and large molecules, and different cell types. The potential clinical relevance of this system was tested with difficult-to-transfect natural killer cell suspensions, and plasmids encoding for the chimeric antigen receptor (CAR), a model of high relevance for adoptive immunotherapy. Our results show significantly higher CAR transfection efficiencies for the DEP-NEP system (>70% vs. <30%), as well as enhanced cell viabilities.

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Yoduro de propidio, ≥94.0% (HPLC)
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Propidium iodide solution
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Calcein-AM, suitable for fluorescence, BioReagent, ≥90% (HPLC)
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Calcein-AM, Small Package (20 X 50 μg ), ≥90.0% (HPLC)
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Calcein AM solution, 4 mM in DMSO, ≥90% (HPLC), solution
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2-Bromo-1-ethyl-pyridinium tetrafluoroborate, ≥97.0% (T)