Abstract

For tissue engineering applications, small interfering RNA (siRNA) is an attractive agent for controlling cellular functions and differentiation. Although polyionic condensation of nucleic acids with polycations has been widely used for gene delivery, siRNA is not strongly associated with cationic carriers due to its low charge density and rigid molecular structures. The use of an excess amount of cationic carriers is often used for siRNA condensation, though they can induce severe cytotoxicity. Here we introduce the self-assembly of siRNA with mild polyelectrolytes into multilayers for efficient gene silencing during cell proliferation. The multilayers were prepared through the sequential layer-by-layer deposition of siRNA and poly-L-lysine (PLL) on a polydopamine-coated substrate. The cells, grown on the siRNA/PLL multilayers, exhibited a remarkable inhibition of the expression of target genes as compared to the use of scrambled siRNA. The gene silencing efficiency depends on the number of siRNA layers within a multilayer. This result indicates that siRNA/PLL multilayers can be potentially utilized for efficient surface-mediated siRNA delivery.

Highlights

  • Among of the current strategy for gene delivery is to form compact and stable nanoparticles via electrostatic interactions between anionic genes and cationic macromolecules[12,13,14]

  • The cells grown on the small interfering RNA (siRNA)/PLL multilayers exhibited the remarkable inhibition of the expression of target genes

  • Preparation of siRNA/PLL multilayers loaded on the PDA-coated substrates

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Summary

Adhesion and Gene Silencing

Small interfering RNA (siRNA) is an attractive agent for controlling cellular functions and differentiation. The gene silencing efficiency depends on the number of siRNA layers within a multilayer This result indicates that siRNA/PLL multilayers can be potentially utilized for efficient surface-mediated siRNA delivery. The PDA layer can mediate the on-surface reduction of metal precursor ions into solid nanostructures because their redox potentials are relatively higher than that of catechol. This property allows PDA to strongly bind to various inorganic surfaces. We employed LBL self-assembly to prepare a siRNA/PLL multilayer on the PDA-coated substrate for surface-mediated siRNA delivery. The surface of siRNA/PLL multilayer induced the effective cell adhesion, spreading and proliferation without any severe cytotoxicity. The gene silencing effect is correlated with the number of a siRNA layer within a siRNA/PLL multilayer

Results and Discussion
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