Chondrogenic Differentiation of Human Mesenchymal Stem Cells via SOX9 Delivery in Cationic Niosomes

Gene transfer to mesenchymal stem cells constitutes a powerful approach to promote their differentiation into the appropriate cartilage phenotype. Although viral vectors represent gold standard vehicles, because of their high efficiency, their use is precluded by important concerns including an elev...

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Main Authors: Natalia Carballo-Pedrares, Clara Sanjurjo-Rodriguez, Jose Señarís, Silvia Díaz-Prado, Ana Rey-Rico
Format: Article
Language:English
Published: MDPI AG 2022-10-01
Series:Pharmaceutics
Subjects:
Online Access:https://www.mdpi.com/1999-4923/14/11/2327
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author Natalia Carballo-Pedrares
Clara Sanjurjo-Rodriguez
Jose Señarís
Silvia Díaz-Prado
Ana Rey-Rico
author_facet Natalia Carballo-Pedrares
Clara Sanjurjo-Rodriguez
Jose Señarís
Silvia Díaz-Prado
Ana Rey-Rico
author_sort Natalia Carballo-Pedrares
collection DOAJ
description Gene transfer to mesenchymal stem cells constitutes a powerful approach to promote their differentiation into the appropriate cartilage phenotype. Although viral vectors represent gold standard vehicles, because of their high efficiency, their use is precluded by important concerns including an elevated immunogenicity and the possibility of insertional mutagenesis. Therefore, the development of new and efficient non-viral vectors is under active investigation. In the present study, we developed new non-viral carriers based on niosomes to promote the effective chondrogenesis of human MSCs. Two different niosome formulations were prepared by varying their composition on non-ionic surfactant, polysorbate 80 solely (P80), or combined with poloxamer 407 (P80PX). The best niosome formulation was proven to transfer a plasmid, encoding for the potent chondrogenic transcription factor SOX9 in hMSC aggregate cultures. Transfection of hMSC aggregates via nioplexes resulted in an increased chondrogenic differentiation with reduced hypertrophy. These results highlight the potential of niosome formulations for gene therapy approaches focused on cartilage repair.
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spelling doaj.art-1cea0cee6f7f4c189d58532e236115312023-11-24T06:20:25ZengMDPI AGPharmaceutics1999-49232022-10-011411232710.3390/pharmaceutics14112327Chondrogenic Differentiation of Human Mesenchymal Stem Cells via SOX9 Delivery in Cationic NiosomesNatalia Carballo-Pedrares0Clara Sanjurjo-Rodriguez1Jose Señarís2Silvia Díaz-Prado3Ana Rey-Rico4Centro de Investigacións Científicas Avanzadas (CICA), Universidade da Coruña, As Carballeiras, s/n. Campus de Elviña, 15071 A Coruña, SpainCentro de Investigacións Científicas Avanzadas (CICA), Universidade da Coruña, As Carballeiras, s/n. Campus de Elviña, 15071 A Coruña, SpainInstitute of Biomedical Research of A Coruña (INIBIC), University Hospital Complex A Coruña (CHUAC), Galician Health Service (SERGAS), 15006 A Coruña, SpainCentro de Investigacións Científicas Avanzadas (CICA), Universidade da Coruña, As Carballeiras, s/n. Campus de Elviña, 15071 A Coruña, SpainCentro de Investigacións Científicas Avanzadas (CICA), Universidade da Coruña, As Carballeiras, s/n. Campus de Elviña, 15071 A Coruña, SpainGene transfer to mesenchymal stem cells constitutes a powerful approach to promote their differentiation into the appropriate cartilage phenotype. Although viral vectors represent gold standard vehicles, because of their high efficiency, their use is precluded by important concerns including an elevated immunogenicity and the possibility of insertional mutagenesis. Therefore, the development of new and efficient non-viral vectors is under active investigation. In the present study, we developed new non-viral carriers based on niosomes to promote the effective chondrogenesis of human MSCs. Two different niosome formulations were prepared by varying their composition on non-ionic surfactant, polysorbate 80 solely (P80), or combined with poloxamer 407 (P80PX). The best niosome formulation was proven to transfer a plasmid, encoding for the potent chondrogenic transcription factor SOX9 in hMSC aggregate cultures. Transfection of hMSC aggregates via nioplexes resulted in an increased chondrogenic differentiation with reduced hypertrophy. These results highlight the potential of niosome formulations for gene therapy approaches focused on cartilage repair.https://www.mdpi.com/1999-4923/14/11/2327niosomesnioplexeshuman mesenchymal stem cellsSOX9chondrogenesis
spellingShingle Natalia Carballo-Pedrares
Clara Sanjurjo-Rodriguez
Jose Señarís
Silvia Díaz-Prado
Ana Rey-Rico
Chondrogenic Differentiation of Human Mesenchymal Stem Cells via SOX9 Delivery in Cationic Niosomes
Pharmaceutics
niosomes
nioplexes
human mesenchymal stem cells
SOX9
chondrogenesis
title Chondrogenic Differentiation of Human Mesenchymal Stem Cells via SOX9 Delivery in Cationic Niosomes
title_full Chondrogenic Differentiation of Human Mesenchymal Stem Cells via SOX9 Delivery in Cationic Niosomes
title_fullStr Chondrogenic Differentiation of Human Mesenchymal Stem Cells via SOX9 Delivery in Cationic Niosomes
title_full_unstemmed Chondrogenic Differentiation of Human Mesenchymal Stem Cells via SOX9 Delivery in Cationic Niosomes
title_short Chondrogenic Differentiation of Human Mesenchymal Stem Cells via SOX9 Delivery in Cationic Niosomes
title_sort chondrogenic differentiation of human mesenchymal stem cells via sox9 delivery in cationic niosomes
topic niosomes
nioplexes
human mesenchymal stem cells
SOX9
chondrogenesis
url https://www.mdpi.com/1999-4923/14/11/2327
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