Antifibrotic and Pro-regenerative Effects of SMAD3 siRNA and Collagen I mRNA-Loaded Lipid Nanoparticles in Human Tenocytes

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Journal Title
Journal ISSN
Volume Title
A1 Alkuperäisartikkeli tieteellisessä aikakauslehdessä
Date
2024-08-09
Major/Subject
Mcode
Degree programme
Language
en
Pages
12
Series
ACS Applied Nano Materials, Volume 7, issue 15, pp. 17736-17747
Abstract
Tendinopathy involves the inflammation and degeneration of the tendon due to repetitive strain injury. Current treatments primarily target inflammation resolution, yet they do not aim at tissue regeneration. In this study, a microfluidics approach is harnessed to develop a platform of lipid nanoparticles (LNPs) loaded simultaneously with SMAD3 siRNA and collagen I mRNA, aiming to explore its potential dual antifibrotic and regenerative effects in human tenocytes. The developed LNPs displayed size homogeneity and colloidal stability and exhibited high cytocompatibility in human tenocytes. Moreover, LNPs allowed for efficient uptake and transfection efficiency of the RNAs. In the in vitro efficacy studies, the gene expression and production of SMAD3 and collagen I were tested by real-time quantitative chain polymerase reaction and immuno- and intracellular staining, revealing collagen I production enhancement, SMAD3 inhibition, and modulation of other tendon repair factors by the LNPs. Overall, the potential of this platform of RNA-loaded LNPs to be used as a dual therapeutic approach to prevent fibrosis and promote tissue remodeling in late stages of tendon diseases was confirmed.
Description
Publisher Copyright: © 2024 The Authors. Published by American Chemical Society.
Keywords
lipid nanoparticles, mRNA, regeneration, siRNA, tendinopathy
Other note
Citation
López-Cerdá, S, Molinaro, G, Tello, R P, Correia, A, Waris, E, Hirvonen, J, Barreto, G & Santos, H A 2024, ' Antifibrotic and Pro-regenerative Effects of SMAD3 siRNA and Collagen I mRNA-Loaded Lipid Nanoparticles in Human Tenocytes ', ACS Applied Nano Materials, vol. 7, no. 15, pp. 17736-17747 . https://doi.org/10.1021/acsanm.4c02996