Iron oxide nanoparticles promote the migration of mesenchymal stem cells to injury sites
Xiuying Li,1,* Zhenhong Wei,1,* Huiying Lv,1 Liya Wu,1 Yingnan Cui,1 Hua Yao,1 Jing Li,1 Hao Zhang,2 Bai Yang,2 Jinlan Jiang1 1Scientific Research Center, China-Japan Union Hospital of Jilin University, Changchun, Jilin, People’s Republic of China; 2State Key Laboratory of Supramolecular...
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Dove Medical Press
2019
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oai:doaj.org-article:89cce189d81e4059a26b02dac790686d2021-12-02T04:04:10ZIron oxide nanoparticles promote the migration of mesenchymal stem cells to injury sites1178-2013https://doaj.org/article/89cce189d81e4059a26b02dac790686d2019-01-01T00:00:00Zhttps://www.dovepress.com/iron-oxide-nanoparticles-promote-the-migration-of-mesenchymal-stem-cel-peer-reviewed-article-IJNhttps://doaj.org/toc/1178-2013Xiuying Li,1,* Zhenhong Wei,1,* Huiying Lv,1 Liya Wu,1 Yingnan Cui,1 Hua Yao,1 Jing Li,1 Hao Zhang,2 Bai Yang,2 Jinlan Jiang1 1Scientific Research Center, China-Japan Union Hospital of Jilin University, Changchun, Jilin, People’s Republic of China; 2State Key Laboratory of Supramolecular Structure and Materials, College of Chemistry, Jilin University, Changchun, Jilin, People’s Republic of China *These authors contributed equally to this work Background: Developing new methods to deliver cells to the injured tissue is a critical factor in translating cell therapeutics research into clinical use; therefore, there is a need for improved cell homing capabilities. Materials and methods: In this study, we demonstrated the effects of labeling rat bone marrow-derived mesenchymal stem cells (MSCs) with fabricated polydopamine (PDA)-capped Fe3O4 (Fe3O4@PDA) superparticles employing preassembled Fe3O4 nanoparticles as the cores. Results: We found that the Fe3O4@PDA composite superparticles exhibited no adverse effects on MSC characteristics. Moreover, iron oxide nanoparticles increased the number of MSCs in the S-phase, their proliferation index and migration ability, and their secretion of vascular endothelial growth factor relative to unlabeled MSCs. Interestingly, nanoparticles not only promoted the expression of C-X-C chemokine receptor 4 but also increased the expression of the migration-related proteins c-Met and C-C motif chemokine receptor 1, which has not been reported previously. Furthermore, the MSC-loaded nanoparticles exhibited improved homing and anti-inflammatory abilities in the absence of external magnetic fields in vivo. Conclusion: These results indicated that iron oxide nanoparticles rendered MSCs more favorable for use in injury treatment with no negative effects on MSC properties, suggesting their potential clinical efficacy. Keywords: mesenchymal stem cells, migration, Fe3O4 nanoparticles, polydopamineLi XWei ZLv HWu LCui YYao HLi JZhang HYang BJiang JDove Medical Pressarticlemesenchymal stem cellsmigrationFe3O4 nanoparticlespolydopamineMedicine (General)R5-920ENInternational Journal of Nanomedicine, Vol Volume 14, Pp 573-589 (2019) |
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mesenchymal stem cells migration Fe3O4 nanoparticles polydopamine Medicine (General) R5-920 |
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mesenchymal stem cells migration Fe3O4 nanoparticles polydopamine Medicine (General) R5-920 Li X Wei Z Lv H Wu L Cui Y Yao H Li J Zhang H Yang B Jiang J Iron oxide nanoparticles promote the migration of mesenchymal stem cells to injury sites |
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Xiuying Li,1,* Zhenhong Wei,1,* Huiying Lv,1 Liya Wu,1 Yingnan Cui,1 Hua Yao,1 Jing Li,1 Hao Zhang,2 Bai Yang,2 Jinlan Jiang1 1Scientific Research Center, China-Japan Union Hospital of Jilin University, Changchun, Jilin, People’s Republic of China; 2State Key Laboratory of Supramolecular Structure and Materials, College of Chemistry, Jilin University, Changchun, Jilin, People’s Republic of China *These authors contributed equally to this work Background: Developing new methods to deliver cells to the injured tissue is a critical factor in translating cell therapeutics research into clinical use; therefore, there is a need for improved cell homing capabilities. Materials and methods: In this study, we demonstrated the effects of labeling rat bone marrow-derived mesenchymal stem cells (MSCs) with fabricated polydopamine (PDA)-capped Fe3O4 (Fe3O4@PDA) superparticles employing preassembled Fe3O4 nanoparticles as the cores. Results: We found that the Fe3O4@PDA composite superparticles exhibited no adverse effects on MSC characteristics. Moreover, iron oxide nanoparticles increased the number of MSCs in the S-phase, their proliferation index and migration ability, and their secretion of vascular endothelial growth factor relative to unlabeled MSCs. Interestingly, nanoparticles not only promoted the expression of C-X-C chemokine receptor 4 but also increased the expression of the migration-related proteins c-Met and C-C motif chemokine receptor 1, which has not been reported previously. Furthermore, the MSC-loaded nanoparticles exhibited improved homing and anti-inflammatory abilities in the absence of external magnetic fields in vivo. Conclusion: These results indicated that iron oxide nanoparticles rendered MSCs more favorable for use in injury treatment with no negative effects on MSC properties, suggesting their potential clinical efficacy. Keywords: mesenchymal stem cells, migration, Fe3O4 nanoparticles, polydopamine |
format |
article |
author |
Li X Wei Z Lv H Wu L Cui Y Yao H Li J Zhang H Yang B Jiang J |
author_facet |
Li X Wei Z Lv H Wu L Cui Y Yao H Li J Zhang H Yang B Jiang J |
author_sort |
Li X |
title |
Iron oxide nanoparticles promote the migration of mesenchymal stem cells to injury sites |
title_short |
Iron oxide nanoparticles promote the migration of mesenchymal stem cells to injury sites |
title_full |
Iron oxide nanoparticles promote the migration of mesenchymal stem cells to injury sites |
title_fullStr |
Iron oxide nanoparticles promote the migration of mesenchymal stem cells to injury sites |
title_full_unstemmed |
Iron oxide nanoparticles promote the migration of mesenchymal stem cells to injury sites |
title_sort |
iron oxide nanoparticles promote the migration of mesenchymal stem cells to injury sites |
publisher |
Dove Medical Press |
publishDate |
2019 |
url |
https://doaj.org/article/89cce189d81e4059a26b02dac790686d |
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