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Long-term MRI tracking of dual-labeled adipose-derived stem cells homing into mouse carotid artery injury

BACKGROUND: Stem cell therapy has shown great promise for regenerative repair of injured or diseased tissues. Adipose-derived stem cells (ADSCs) have become increasingly attractive candidates for cellular therapy. Magnetic resonance imaging has been proven to be effective in tracking magnetic-labele...

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Autores principales: Qin, Jin-Bao, Li, Kang-An, Li, Xiang-Xiang, Xie, Qing-Song, Lin, Jia-Ying, Ye, Kai-Chuang, Jiang, Mi-Er, Zhang, Gui-Xiang, Lu, Xin-Wu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3487538/
https://www.ncbi.nlm.nih.gov/pubmed/23125528
http://dx.doi.org/10.2147/IJN.S35647
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author Qin, Jin-Bao
Li, Kang-An
Li, Xiang-Xiang
Xie, Qing-Song
Lin, Jia-Ying
Ye, Kai-Chuang
Jiang, Mi-Er
Zhang, Gui-Xiang
Lu, Xin-Wu
author_facet Qin, Jin-Bao
Li, Kang-An
Li, Xiang-Xiang
Xie, Qing-Song
Lin, Jia-Ying
Ye, Kai-Chuang
Jiang, Mi-Er
Zhang, Gui-Xiang
Lu, Xin-Wu
author_sort Qin, Jin-Bao
collection PubMed
description BACKGROUND: Stem cell therapy has shown great promise for regenerative repair of injured or diseased tissues. Adipose-derived stem cells (ADSCs) have become increasingly attractive candidates for cellular therapy. Magnetic resonance imaging has been proven to be effective in tracking magnetic-labeled cells and evaluating their clinical relevance after cell transplantation. This study investigated the feasibility of imaging green fluorescent protein-expressing ADSCs (GFP-ADSCs) labeled with superparamagnetic iron oxide particles, and tracked them in vivo with noninvasive magnetic resonance imaging after cell transplantation in a model of mouse carotid artery injury. METHODS: GFP-ADSCs were isolated from the adipose tissues of GFP mice and labeled with superparamagnetic iron oxide particles. Intracellular stability, proliferation, and viability of the labeled cells were evaluated in vitro. Next, the cells were transplanted into a mouse carotid artery injury model. Clinical 3 T magnetic resonance imaging was performed immediately before and 1, 3, 7, 14, 21, and 30 days after cell transplantation. Prussian blue staining and histological analysis were performed 7 and 30 days after transplantation. RESULTS: GFP-ADSCs were found to be efficiently labeled with superparamagnetic iron oxide particles, with no effect on viability and proliferation. Homing of the labeled cells into the injured carotid artery tissue could be monitored by magnetic resonance imaging. CONCLUSION: Magnetically labeled ADSCs with expression of GFP can home into sites of vascular injury, and may provide new insights into understanding of cell-based therapy for cardiovascular lesions.
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spelling pubmed-34875382012-11-03 Long-term MRI tracking of dual-labeled adipose-derived stem cells homing into mouse carotid artery injury Qin, Jin-Bao Li, Kang-An Li, Xiang-Xiang Xie, Qing-Song Lin, Jia-Ying Ye, Kai-Chuang Jiang, Mi-Er Zhang, Gui-Xiang Lu, Xin-Wu Int J Nanomedicine Original Research BACKGROUND: Stem cell therapy has shown great promise for regenerative repair of injured or diseased tissues. Adipose-derived stem cells (ADSCs) have become increasingly attractive candidates for cellular therapy. Magnetic resonance imaging has been proven to be effective in tracking magnetic-labeled cells and evaluating their clinical relevance after cell transplantation. This study investigated the feasibility of imaging green fluorescent protein-expressing ADSCs (GFP-ADSCs) labeled with superparamagnetic iron oxide particles, and tracked them in vivo with noninvasive magnetic resonance imaging after cell transplantation in a model of mouse carotid artery injury. METHODS: GFP-ADSCs were isolated from the adipose tissues of GFP mice and labeled with superparamagnetic iron oxide particles. Intracellular stability, proliferation, and viability of the labeled cells were evaluated in vitro. Next, the cells were transplanted into a mouse carotid artery injury model. Clinical 3 T magnetic resonance imaging was performed immediately before and 1, 3, 7, 14, 21, and 30 days after cell transplantation. Prussian blue staining and histological analysis were performed 7 and 30 days after transplantation. RESULTS: GFP-ADSCs were found to be efficiently labeled with superparamagnetic iron oxide particles, with no effect on viability and proliferation. Homing of the labeled cells into the injured carotid artery tissue could be monitored by magnetic resonance imaging. CONCLUSION: Magnetically labeled ADSCs with expression of GFP can home into sites of vascular injury, and may provide new insights into understanding of cell-based therapy for cardiovascular lesions. Dove Medical Press 2012 2012-10-02 /pmc/articles/PMC3487538/ /pubmed/23125528 http://dx.doi.org/10.2147/IJN.S35647 Text en © 2012 Qin et al, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Original Research
Qin, Jin-Bao
Li, Kang-An
Li, Xiang-Xiang
Xie, Qing-Song
Lin, Jia-Ying
Ye, Kai-Chuang
Jiang, Mi-Er
Zhang, Gui-Xiang
Lu, Xin-Wu
Long-term MRI tracking of dual-labeled adipose-derived stem cells homing into mouse carotid artery injury
title Long-term MRI tracking of dual-labeled adipose-derived stem cells homing into mouse carotid artery injury
title_full Long-term MRI tracking of dual-labeled adipose-derived stem cells homing into mouse carotid artery injury
title_fullStr Long-term MRI tracking of dual-labeled adipose-derived stem cells homing into mouse carotid artery injury
title_full_unstemmed Long-term MRI tracking of dual-labeled adipose-derived stem cells homing into mouse carotid artery injury
title_short Long-term MRI tracking of dual-labeled adipose-derived stem cells homing into mouse carotid artery injury
title_sort long-term mri tracking of dual-labeled adipose-derived stem cells homing into mouse carotid artery injury
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3487538/
https://www.ncbi.nlm.nih.gov/pubmed/23125528
http://dx.doi.org/10.2147/IJN.S35647
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