In vitro transfection of bone marrow-derived dendritic cells with TATp-liposomes

Juan Sebastián Pappalardo,^1–3 Cecilia A Langellotti,² Sebastián Di Giacomo,¹ Valeria Olivera,¹ Valeria Quattrocchi,² Patricia I Zamorano,^1,2 William C Hartner,³ Tatyana S Levchenko,³ Vladimir P Torchilin<sup>3

1</sup>Virology Institute, Center for Research in Veterinary and Agronomic Sciences, National Institute for Agricultural Technology (INTA), Hurlingham, BA, Argentina; ²National Council for Scientific and Technical Research (CONICET), Autonomous City of Buenos Aires, Argentina; ³Center for Pharmaceutical Biotechnology and Nanomedicine, Northeastern University, Boston, MA, USA

Abstract: Dendritic cells (DC) are antigen-presenting cells uniquely capable of priming naïve T cells and cross-presenting antigens, and they determine the type of immune response elicited against an antigen. TAT peptide (TATp), is an amphipathic, arginine-rich, cationic peptide that promotes penetration and translocation of various molecules and nanoparticles into cells. TATp-liposomes (TATp-L) used for DC transfection were prepared using TATp derivatized with a lipid-terminated polymer capable of anchoring in the liposomal membrane. Here, we show that the addition of TATp to DNA-loaded liposomes increased the uptake of DNA in DC. DNA-loaded TATp-L increased the in vitro transfection efficiency in DC cultures as evidenced by a higher expression of the enhanced green fluorescent protein and bovine herpes virus type 1 glycoprotein D (gD). The de novo synthesized gD protein was immunologically stimulating when transfections were performed with TATp-L, as indicated by the secretion of interleukin 6.

Keywords: dendritic cell transfection, green fluorescent protein, bovine herpes virus 1 glycoprotein D, liposomes, TAT peptide, interleukin 6

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