| Literature DB >> 30644615 |
Maruthibabu Paidikondala1, Vignesh Kumar Rangasami2, Ganesh N Nawale1, Tommaso Casalini3,4, Giuseppe Perale3, Sandeep Kadekar1, Gaurav Mohanty5, Turkka Salminen6, Oommen P Oommen2, Oommen P Varghese1.
Abstract
Circulating nucleic acids, such as short interfering RNA (siRNA), regulate many biological processes; however, the mechanism by which these molecules enter the cell is poorly understood. The role of extracellular-matrix-derived polymers in binding siRNAs and trafficking them across the plasma membrane is reported. Thermal melting, dynamic light scattering, scanning electron microscopy, and computational analysis indicate that hyaluronic acid can stabilize siRNA via hydrogen bonding and Van der Waals interactions. This stabilization facilitated HA size- and concentration-dependent gene silencing in a CD44-positive human osteosarcoma cell line (MG-63) and in human mesenchymal stromal cells (hMSCs). This native HA-based siRNA transfection represents the first report on an anionic, non-viral delivery method that resulted in approximately 60 % gene knockdown in both cell types tested, which correlated with a reduction in translation levels.Entities:
Keywords: RNAi; extracellular matrix; hyaluronic acid; nanoparticles; transfection
Year: 2019 PMID: 30644615 DOI: 10.1002/anie.201900099
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336