Vibropolyfection: coupling polymer-mediated gene delivery to mechanical stimulation to enhance transfection of adherent cells

• Published in: Journal of nanobiotechnology 2022-08, Vol.20 (1), p.363-19, Article 363
• Main Authors: Ponti, Federica, Bono, Nina, Russo, Luca, Bigini, Paolo, Mantovani, Diego, Candiani, Gabriele
• Format: Article
• Language: English
• Subjects: Adherent cells; Analysis; Apoptosis; Cell culture; Cell growth; Cell lines; Cell proliferation; Clathrin; Coronaviruses; COVID-19; COVID-19 Vaccines; Cytology; Effectiveness; Gene expression; Gene transfer; Gene Transfer Techniques; Genetic aspects; Health aspects; Humans; Mechanical stimulation; Mechanical stimuli; Morphology; Nanoparticles; New technology; Non-viral gene delivery; Nucleic acids; Plasma; Plasma membranes; Polyethyleneimine; Polymers; Priming; Stimulation; Transfection; Vaccines; Vectors (Biology); Vibratory loads
• ISSN: 1477-3155; 1477-3155
• DOI: 10.1186/s12951-022-01571-x

With the success of recent non-viral gene delivery-based COVID-19 vaccines, nanovectors have gained some public acceptance and come to the forefront of advanced therapies. Unfortunately, the relatively low ability of the vectors to overcome cellular barriers adversely affects their effectiveness. Scientists have thus been striving to develop ever more effective gene delivery vectors, but the results are still far from satisfactory. Therefore, developing novel strategies is probably the only way forward to bring about genuine change. Herein, we devise a brand-new gene delivery strategy to boost dramatically the transfection efficiency of two gold standard nucleic acid (NA)/polymer nanoparticles (polyplexes) in vitro. We conceived a device to generate milli-to-nanoscale vibrational cues as a function of the frequency set, and deliver vertical uniaxial displacements to adherent cells in culture. A short-lived high-frequency vibrational load (t = 5 min, f = 1,000 Hz) caused abrupt and extensive plasmalemma outgrowths but was safe for cells as neither cell proliferation rate nor viability was affected. Cells took about 1 hr to revert to quasi-naïve morphology through plasma membrane remodeling. In turn, this eventually triggered the mechano-activated clathrin-mediated endocytic pathway and made cells more apt to internalize polyplexes, resulting in transfection efficiencies increased from 10-to-100-fold. Noteworthy, these results were obtained transfecting three cell lines and hard-to-transfect primary cells. In this work, we focus on a new technology to enhance the intracellular delivery of NAs and improve the transfection efficiency of non-viral vectors through priming adherent cells with a short vibrational stimulation. This study paves the way for capitalizing on physical cell stimulation(s) to significantly raise the effectiveness of gene delivery vectors in vitro and ex vivo.