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Effects of miR-26a on Osteogenic Differentiation of Bone Marrow Mesenchymal Stem Cells by a Mesoporous Silica Nanoparticle - PEI - Peptide System

INTRODUCTION: RNA-based therapy for bone repair and regeneration is a highly safe and effective approach, which has been extensively investigated in recent years. However, the molecular stability of RNA agents still remains insufficient for clinical application. High porosity, tunable size, and idea...

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Autores principales: Yan, Jia, Lu, Xiaoli, Zhu, Xinchen, Hu, Xiaokun, Wang, Lili, Qian, Jun, Zhang, Feimin, Liu, Mei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6986258/
https://www.ncbi.nlm.nih.gov/pubmed/32158207
http://dx.doi.org/10.2147/IJN.S228797
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author Yan, Jia
Lu, Xiaoli
Zhu, Xinchen
Hu, Xiaokun
Wang, Lili
Qian, Jun
Zhang, Feimin
Liu, Mei
author_facet Yan, Jia
Lu, Xiaoli
Zhu, Xinchen
Hu, Xiaokun
Wang, Lili
Qian, Jun
Zhang, Feimin
Liu, Mei
author_sort Yan, Jia
collection PubMed
description INTRODUCTION: RNA-based therapy for bone repair and regeneration is a highly safe and effective approach, which has been extensively investigated in recent years. However, the molecular stability of RNA agents still remains insufficient for clinical application. High porosity, tunable size, and ideal biodegradability and biosafety are a few of the characters of mesoporous silicon nanoparticles (MSNs) that render them a promising biomaterial carrier for RNA treatment. MATERIALS AND METHODS: In this study, a novel miR-26a delivery system was constructed based on MSNs. Next, we assessed the miRNA protection of the delivery vehicles. Then, rat bone marrow mesenchymal stem cells (rBMSCs) were incubated with the vectors, and the transfection efficiency, cellular uptake, and effects on cell viability and osteogenic differentiation were evaluated. RESULTS: The results demonstrated that the vectors protected miR-26a from degradation in vitro and delivered it into the cytoplasm. A relatively low concentration of the delivery systems significantly increased osteogenic differentiation of rBMSCs. CONCLUSION: The vectors constructed in our study provide new methods and strategies for the delivery of microRNAs in bone tissue engineering.
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spelling pubmed-69862582020-03-10 Effects of miR-26a on Osteogenic Differentiation of Bone Marrow Mesenchymal Stem Cells by a Mesoporous Silica Nanoparticle - PEI - Peptide System Yan, Jia Lu, Xiaoli Zhu, Xinchen Hu, Xiaokun Wang, Lili Qian, Jun Zhang, Feimin Liu, Mei Int J Nanomedicine Original Research INTRODUCTION: RNA-based therapy for bone repair and regeneration is a highly safe and effective approach, which has been extensively investigated in recent years. However, the molecular stability of RNA agents still remains insufficient for clinical application. High porosity, tunable size, and ideal biodegradability and biosafety are a few of the characters of mesoporous silicon nanoparticles (MSNs) that render them a promising biomaterial carrier for RNA treatment. MATERIALS AND METHODS: In this study, a novel miR-26a delivery system was constructed based on MSNs. Next, we assessed the miRNA protection of the delivery vehicles. Then, rat bone marrow mesenchymal stem cells (rBMSCs) were incubated with the vectors, and the transfection efficiency, cellular uptake, and effects on cell viability and osteogenic differentiation were evaluated. RESULTS: The results demonstrated that the vectors protected miR-26a from degradation in vitro and delivered it into the cytoplasm. A relatively low concentration of the delivery systems significantly increased osteogenic differentiation of rBMSCs. CONCLUSION: The vectors constructed in our study provide new methods and strategies for the delivery of microRNAs in bone tissue engineering. Dove 2020-01-23 /pmc/articles/PMC6986258/ /pubmed/32158207 http://dx.doi.org/10.2147/IJN.S228797 Text en © 2020 Yan et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Yan, Jia
Lu, Xiaoli
Zhu, Xinchen
Hu, Xiaokun
Wang, Lili
Qian, Jun
Zhang, Feimin
Liu, Mei
Effects of miR-26a on Osteogenic Differentiation of Bone Marrow Mesenchymal Stem Cells by a Mesoporous Silica Nanoparticle - PEI - Peptide System
title Effects of miR-26a on Osteogenic Differentiation of Bone Marrow Mesenchymal Stem Cells by a Mesoporous Silica Nanoparticle - PEI - Peptide System
title_full Effects of miR-26a on Osteogenic Differentiation of Bone Marrow Mesenchymal Stem Cells by a Mesoporous Silica Nanoparticle - PEI - Peptide System
title_fullStr Effects of miR-26a on Osteogenic Differentiation of Bone Marrow Mesenchymal Stem Cells by a Mesoporous Silica Nanoparticle - PEI - Peptide System
title_full_unstemmed Effects of miR-26a on Osteogenic Differentiation of Bone Marrow Mesenchymal Stem Cells by a Mesoporous Silica Nanoparticle - PEI - Peptide System
title_short Effects of miR-26a on Osteogenic Differentiation of Bone Marrow Mesenchymal Stem Cells by a Mesoporous Silica Nanoparticle - PEI - Peptide System
title_sort effects of mir-26a on osteogenic differentiation of bone marrow mesenchymal stem cells by a mesoporous silica nanoparticle - pei - peptide system
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6986258/
https://www.ncbi.nlm.nih.gov/pubmed/32158207
http://dx.doi.org/10.2147/IJN.S228797
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