RT Journal Article
SR Electronic
T1 Viable and efficient electroporation-based genetic manipulation of unstimulated human T cells
JF bioRxiv
FD Cold Spring Harbor Laboratory
SP 466243
DO 10.1101/466243
A1 Pinar Aksoy
A1 Bülent Arman Aksoy
A1 Eric Czech
A1 Jeff Hammerbacher
YR 2019
UL http://biorxiv.org/content/early/2019/10/20/466243.abstract
AB Electroporation is the most feasible non-viral material delivery system for manipulating human T cells given its time- and cost-effectiveness. However, efficient delivery requires electroporation settings to be optimized for different devices, cellular states, and materials to be delivered. Here, we used electroporation to either induce exogenous gene expression in human primary T cells by plasmids or in vitro transcribed (IVT) mRNA and also target endogenous genes by Cas9 ribonucleoproteins (RNPs). We characterized the electroporation conditions both for activated and unstimulated human T cells. Although naive cells are non-dividing and therefore their genetic manipulation is harder compared to activated T cells, we developed the technical ability to manipulate both naive and memory cells within the unstimulated T cell population by IVT mRNA and Cas9 RNP electroporation. Here, we outline the best practices for achieving highly-efficient genetic manipulation in primary T cells without causing significant cytotoxicity to the cells. Because there is increasing evidence for “less-differentiated” T cells to have better anti-tumor activity for immunotherapy, manipulating naive T cells with high efficiency is also of high importance to clinical applications and to study the biology of these cells.