Cargando…

Comparison of osteogenic differentiation induced by siNoggin and pBMP-2 delivered by lipopolysaccharide-amine nanopolymersomes and underlying molecular mechanisms

Purpose: Gene therapies via Noggin small interfering (si)RNA (siNoggin) and bone morphogenetic protein (BMP)-2 plasmid DNA (pBMP-2) may be promising strategies for bone repair/regeneration, but their ideal delivery vectors, efficacy difference, and underlying mechanisms have not been explored, so th...

Descripción completa

Detalles Bibliográficos
Autores principales: Huang, Mingdi, Zhang, Xinchun, Li, Jing, Li, Yanshan, Wang, Qinmei, Teng, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6559258/
https://www.ncbi.nlm.nih.gov/pubmed/31239677
http://dx.doi.org/10.2147/IJN.S203540
_version_ 1783425798449922048
author Huang, Mingdi
Zhang, Xinchun
Li, Jing
Li, Yanshan
Wang, Qinmei
Teng, Wei
author_facet Huang, Mingdi
Zhang, Xinchun
Li, Jing
Li, Yanshan
Wang, Qinmei
Teng, Wei
author_sort Huang, Mingdi
collection PubMed
description Purpose: Gene therapies via Noggin small interfering (si)RNA (siNoggin) and bone morphogenetic protein (BMP)-2 plasmid DNA (pBMP-2) may be promising strategies for bone repair/regeneration, but their ideal delivery vectors, efficacy difference, and underlying mechanisms have not been explored, so these issues were probed here. Methods: This study used lipopolysaccharide-amine nanopolymersomes (LNPs), an efficient cytosolic delivery vector developed by the research team, to mediate siNoggin and pBMP-2 to transfect MC3T3-E1 cells, respectively. The cytotoxicity, cell uptake, and gene knockdown efficiency of siNoggin-loaded LNPs (LNPs/siNoggin) were studied, then the osteogenic-differentiation efficacy of MC3T3-E1 cells treated by LNPs/pBMP-2 and LNPs/siNoggin, respectively, were compared by measuring the expression of osteogenesis-related genes and proteins, alkaline phosphatase (ALP) activity, and mineralization of the extracellular matrix at all osteogenic stages. Finally, the possible signaling pathways of the two treatments were explored. Results: LNPs delivered siNoggin into cells efficiently to silence 50% of Noggin expression without obvious cytotoxicity. LNPs/siNoggin and LNPs/pBMP-2 enhanced the osteogenic differentiation of MC3T3 E1 cells, but LNPs/siNoggin was better than LNPs/pBMP-2. BMP/Mothers against decapentaplegic homolog (Smad) and glycogen synthase kinase (GSK)-3β/β-catenin signaling pathways appeared to be involved in osteogenic differentiation induced by LNPs/siNoggin, but GSK-3β/β-catenin was not stimulated upon LNPs/pBMP-2 treatment. Conclusion: LNPs are safe and efficient delivery vectors for DNA and RNA, which may find wide applications in gene therapy. siNoggin treatment may be a more efficient strategy to enhance osteogenic differentiation than pBMP-2 treatment. LNPs loaded with siNoggin and/or pBMP-2 may provide new opportunities for the repair and regeneration of bone.
format Online
Article
Text
id pubmed-6559258
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Dove
record_format MEDLINE/PubMed
spelling pubmed-65592582019-06-25 Comparison of osteogenic differentiation induced by siNoggin and pBMP-2 delivered by lipopolysaccharide-amine nanopolymersomes and underlying molecular mechanisms Huang, Mingdi Zhang, Xinchun Li, Jing Li, Yanshan Wang, Qinmei Teng, Wei Int J Nanomedicine Original Research Purpose: Gene therapies via Noggin small interfering (si)RNA (siNoggin) and bone morphogenetic protein (BMP)-2 plasmid DNA (pBMP-2) may be promising strategies for bone repair/regeneration, but their ideal delivery vectors, efficacy difference, and underlying mechanisms have not been explored, so these issues were probed here. Methods: This study used lipopolysaccharide-amine nanopolymersomes (LNPs), an efficient cytosolic delivery vector developed by the research team, to mediate siNoggin and pBMP-2 to transfect MC3T3-E1 cells, respectively. The cytotoxicity, cell uptake, and gene knockdown efficiency of siNoggin-loaded LNPs (LNPs/siNoggin) were studied, then the osteogenic-differentiation efficacy of MC3T3-E1 cells treated by LNPs/pBMP-2 and LNPs/siNoggin, respectively, were compared by measuring the expression of osteogenesis-related genes and proteins, alkaline phosphatase (ALP) activity, and mineralization of the extracellular matrix at all osteogenic stages. Finally, the possible signaling pathways of the two treatments were explored. Results: LNPs delivered siNoggin into cells efficiently to silence 50% of Noggin expression without obvious cytotoxicity. LNPs/siNoggin and LNPs/pBMP-2 enhanced the osteogenic differentiation of MC3T3 E1 cells, but LNPs/siNoggin was better than LNPs/pBMP-2. BMP/Mothers against decapentaplegic homolog (Smad) and glycogen synthase kinase (GSK)-3β/β-catenin signaling pathways appeared to be involved in osteogenic differentiation induced by LNPs/siNoggin, but GSK-3β/β-catenin was not stimulated upon LNPs/pBMP-2 treatment. Conclusion: LNPs are safe and efficient delivery vectors for DNA and RNA, which may find wide applications in gene therapy. siNoggin treatment may be a more efficient strategy to enhance osteogenic differentiation than pBMP-2 treatment. LNPs loaded with siNoggin and/or pBMP-2 may provide new opportunities for the repair and regeneration of bone. Dove 2019-06-06 /pmc/articles/PMC6559258/ /pubmed/31239677 http://dx.doi.org/10.2147/IJN.S203540 Text en © 2019 Huang 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
Huang, Mingdi
Zhang, Xinchun
Li, Jing
Li, Yanshan
Wang, Qinmei
Teng, Wei
Comparison of osteogenic differentiation induced by siNoggin and pBMP-2 delivered by lipopolysaccharide-amine nanopolymersomes and underlying molecular mechanisms
title Comparison of osteogenic differentiation induced by siNoggin and pBMP-2 delivered by lipopolysaccharide-amine nanopolymersomes and underlying molecular mechanisms
title_full Comparison of osteogenic differentiation induced by siNoggin and pBMP-2 delivered by lipopolysaccharide-amine nanopolymersomes and underlying molecular mechanisms
title_fullStr Comparison of osteogenic differentiation induced by siNoggin and pBMP-2 delivered by lipopolysaccharide-amine nanopolymersomes and underlying molecular mechanisms
title_full_unstemmed Comparison of osteogenic differentiation induced by siNoggin and pBMP-2 delivered by lipopolysaccharide-amine nanopolymersomes and underlying molecular mechanisms
title_short Comparison of osteogenic differentiation induced by siNoggin and pBMP-2 delivered by lipopolysaccharide-amine nanopolymersomes and underlying molecular mechanisms
title_sort comparison of osteogenic differentiation induced by sinoggin and pbmp-2 delivered by lipopolysaccharide-amine nanopolymersomes and underlying molecular mechanisms
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6559258/
https://www.ncbi.nlm.nih.gov/pubmed/31239677
http://dx.doi.org/10.2147/IJN.S203540
work_keys_str_mv AT huangmingdi comparisonofosteogenicdifferentiationinducedbysinogginandpbmp2deliveredbylipopolysaccharideaminenanopolymersomesandunderlyingmolecularmechanisms
AT zhangxinchun comparisonofosteogenicdifferentiationinducedbysinogginandpbmp2deliveredbylipopolysaccharideaminenanopolymersomesandunderlyingmolecularmechanisms
AT lijing comparisonofosteogenicdifferentiationinducedbysinogginandpbmp2deliveredbylipopolysaccharideaminenanopolymersomesandunderlyingmolecularmechanisms
AT liyanshan comparisonofosteogenicdifferentiationinducedbysinogginandpbmp2deliveredbylipopolysaccharideaminenanopolymersomesandunderlyingmolecularmechanisms
AT wangqinmei comparisonofosteogenicdifferentiationinducedbysinogginandpbmp2deliveredbylipopolysaccharideaminenanopolymersomesandunderlyingmolecularmechanisms
AT tengwei comparisonofosteogenicdifferentiationinducedbysinogginandpbmp2deliveredbylipopolysaccharideaminenanopolymersomesandunderlyingmolecularmechanisms