Evans, MG, Al-Shakli, A, Jenkins, SI and Chari, DM (2017) Electrophysiological Assessment of Primary Cortical Neurons Genetically Engineered using Iron Oxide Nanoparticles. Nano Research, 10 (8). pp. 2881-2890. ISSN 1998-0000

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The development of safe technologies to genetically modify neurons is of great interest in regenerative neurology, for both translational and basic science applications. Such approaches have conventionally been heavily reliant on viral transduction methods, which have safety and production limitations. Magnetofection (magnet-assisted gene transfer using iron oxide nanoparticles as vectors) has emerged as a highly promising non-viral alternative for safe and reproducible genetic modification of neurons. Despite the high potential of this technology, there is an important gap in our knowledge of the safety of this approach, namely, whether it alters neuronal function in adverse ways, such as by altering neuronal excitability and signaling. We have investigated the effects of magnetofection in primary cortical neurons by examining neuronal excitability using the whole cell patch clamp technique. We found no evidence that magnetofection alters the voltage-dependent sodium and potassium ionic currents that underpin excitability. Our study provides important new data supporting magnetofection as a safe technology for bioengineering of neuronal cell populations.

Item Type: Article
Additional Information: This is the accepted author manuscript (AAM). The final published version (version of record) is available online via Springer at http://dx.doi.org/ 10.1007/s12274-017-1496-4 Please refer to any applicable terms of use of the publisher.
Uncontrolled Keywords: transfection magnetic nanoparticle green fluorescent protein (GFP) whole-cell patch clamp fluorescence microscopy
Subjects: R Medicine > R Medicine (General)
Divisions: Faculty of Medicine and Health Sciences > Institute for Science and Technology in Medicine
Depositing User: Symplectic
Date Deposited: 11 Apr 2017 13:37
Last Modified: 13 Jun 2018 13:23
URI: https://eprints.keele.ac.uk/id/eprint/2626

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