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Delivery of coenzyme Q10 loaded micelle targets mitochondrial ROS and enhances efficiency of mesenchymal stem cell therapy in intervertebral disc degeneration

Stem cell transplantation has been proved a promising therapeutic instrument in intervertebral disc degeneration (IVDD). However, the elevation of oxidative stress in the degenerated region impairs the efficiency of mesenchymal stem cells (BMSCs) transplantation treatment via exaggeration of mitocho...

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Autores principales: Sun, Junyuan, Yang, Fei, Wang, Lianlei, Yu, Haichao, Yang, Zhijie, Wei, Jingjing, Vasilev, Krasimir, Zhang, Xuesong, Liu, Xinyu, Zhao, Yunpeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: KeAi Publishing 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9676151/
https://www.ncbi.nlm.nih.gov/pubmed/36439087
http://dx.doi.org/10.1016/j.bioactmat.2022.10.019
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author Sun, Junyuan
Yang, Fei
Wang, Lianlei
Yu, Haichao
Yang, Zhijie
Wei, Jingjing
Vasilev, Krasimir
Zhang, Xuesong
Liu, Xinyu
Zhao, Yunpeng
author_facet Sun, Junyuan
Yang, Fei
Wang, Lianlei
Yu, Haichao
Yang, Zhijie
Wei, Jingjing
Vasilev, Krasimir
Zhang, Xuesong
Liu, Xinyu
Zhao, Yunpeng
author_sort Sun, Junyuan
collection PubMed
description Stem cell transplantation has been proved a promising therapeutic instrument in intervertebral disc degeneration (IVDD). However, the elevation of oxidative stress in the degenerated region impairs the efficiency of mesenchymal stem cells (BMSCs) transplantation treatment via exaggeration of mitochondrial ROS and promotion of BMSCs apoptosis. Herein, we applied an emulsion-confined assembly method to encapsulate Coenzyme Q10 (Co-Q10), a promising hydrophobic antioxidant which targets mitochondria ROS, into the lecithin micelles, which renders the insoluble Co-Q10 dispersible in water as stable colloids. These micelles are injectable, which displayed efficient ability to facilitate Co-Q10 to get into BMSCs in vitro, and exhibited prolonged release of Co-Q10 in intervertebral disc tissue of animal models. Compared to mere use of Co-Q10, the Co-Q10 loaded micelle possessed better bioactivities, which elevated the viability, restored mitochondrial structure as well as function, and enhanced production of ECM components in rat BMSCs. Moreover, it is demonstrated that the injection of this micelle with BMSCs retained disc height and alleviated IVDD in a rat needle puncture model. Therefore, these Co-Q10 loaded micelles play a protective role in cell survival and differentiation through antagonizing mitochondrial ROS, and might be a potential therapeutic agent for IVDD.
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spelling pubmed-96761512022-11-25 Delivery of coenzyme Q10 loaded micelle targets mitochondrial ROS and enhances efficiency of mesenchymal stem cell therapy in intervertebral disc degeneration Sun, Junyuan Yang, Fei Wang, Lianlei Yu, Haichao Yang, Zhijie Wei, Jingjing Vasilev, Krasimir Zhang, Xuesong Liu, Xinyu Zhao, Yunpeng Bioact Mater Article Stem cell transplantation has been proved a promising therapeutic instrument in intervertebral disc degeneration (IVDD). However, the elevation of oxidative stress in the degenerated region impairs the efficiency of mesenchymal stem cells (BMSCs) transplantation treatment via exaggeration of mitochondrial ROS and promotion of BMSCs apoptosis. Herein, we applied an emulsion-confined assembly method to encapsulate Coenzyme Q10 (Co-Q10), a promising hydrophobic antioxidant which targets mitochondria ROS, into the lecithin micelles, which renders the insoluble Co-Q10 dispersible in water as stable colloids. These micelles are injectable, which displayed efficient ability to facilitate Co-Q10 to get into BMSCs in vitro, and exhibited prolonged release of Co-Q10 in intervertebral disc tissue of animal models. Compared to mere use of Co-Q10, the Co-Q10 loaded micelle possessed better bioactivities, which elevated the viability, restored mitochondrial structure as well as function, and enhanced production of ECM components in rat BMSCs. Moreover, it is demonstrated that the injection of this micelle with BMSCs retained disc height and alleviated IVDD in a rat needle puncture model. Therefore, these Co-Q10 loaded micelles play a protective role in cell survival and differentiation through antagonizing mitochondrial ROS, and might be a potential therapeutic agent for IVDD. KeAi Publishing 2022-11-16 /pmc/articles/PMC9676151/ /pubmed/36439087 http://dx.doi.org/10.1016/j.bioactmat.2022.10.019 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Sun, Junyuan
Yang, Fei
Wang, Lianlei
Yu, Haichao
Yang, Zhijie
Wei, Jingjing
Vasilev, Krasimir
Zhang, Xuesong
Liu, Xinyu
Zhao, Yunpeng
Delivery of coenzyme Q10 loaded micelle targets mitochondrial ROS and enhances efficiency of mesenchymal stem cell therapy in intervertebral disc degeneration
title Delivery of coenzyme Q10 loaded micelle targets mitochondrial ROS and enhances efficiency of mesenchymal stem cell therapy in intervertebral disc degeneration
title_full Delivery of coenzyme Q10 loaded micelle targets mitochondrial ROS and enhances efficiency of mesenchymal stem cell therapy in intervertebral disc degeneration
title_fullStr Delivery of coenzyme Q10 loaded micelle targets mitochondrial ROS and enhances efficiency of mesenchymal stem cell therapy in intervertebral disc degeneration
title_full_unstemmed Delivery of coenzyme Q10 loaded micelle targets mitochondrial ROS and enhances efficiency of mesenchymal stem cell therapy in intervertebral disc degeneration
title_short Delivery of coenzyme Q10 loaded micelle targets mitochondrial ROS and enhances efficiency of mesenchymal stem cell therapy in intervertebral disc degeneration
title_sort delivery of coenzyme q10 loaded micelle targets mitochondrial ros and enhances efficiency of mesenchymal stem cell therapy in intervertebral disc degeneration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9676151/
https://www.ncbi.nlm.nih.gov/pubmed/36439087
http://dx.doi.org/10.1016/j.bioactmat.2022.10.019
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