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Implantation of Ferumoxides Labeled Human Mesenchymal Stem Cells in Cartilage Defects
The field of tissue engineering integrates the principles of engineering, cell biology and medicine towards the regeneration of specific cells and functional tissue. Matrix associated stem cell implants (MASI) aim to regenerate cartilage defects due to arthritic or traumatic joint injuries. Adult me...
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Formato: | Texto |
Lenguaje: | English |
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MyJove Corporation
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2900275/ https://www.ncbi.nlm.nih.gov/pubmed/20368696 http://dx.doi.org/10.3791/1793 |
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author | Nedopil, Alexander J. Mandrussow, Lydia G. Daldrup-Link, Heike E. |
author_facet | Nedopil, Alexander J. Mandrussow, Lydia G. Daldrup-Link, Heike E. |
author_sort | Nedopil, Alexander J. |
collection | PubMed |
description | The field of tissue engineering integrates the principles of engineering, cell biology and medicine towards the regeneration of specific cells and functional tissue. Matrix associated stem cell implants (MASI) aim to regenerate cartilage defects due to arthritic or traumatic joint injuries. Adult mesenchymal stem cells (MSCs) have the ability to differentiate into cells of the chondrogenic lineage and have shown promising results for cell-based articular cartilage repair technologies. Autologous MSCs can be isolated from a variety of tissues, can be expanded in cell cultures without losing their differentiation potential, and have demonstrated chondrogenic differentiation in vitro and in vivo(1, 2). In order to provide local retention and viability of transplanted MSCs in cartilage defects, a scaffold is needed, which also supports subsequent differentiation and proliferation. The architecture of the scaffold guides tissue formation and permits the extracellular matrix, produced by the stem cells, to expand. Previous investigations have shown that a 2% agarose scaffold may support the development of stable hyaline cartilage and does not induce immune responses(3). Long term retention of transplanted stem cells in MASI is critical for cartilage regeneration. Labeling of MSCs with iron oxide nanoparticles allows for long-term in vivo tracking with non-invasive MR imaging techniques(4). This presentation will demonstrate techniques for labeling MSCs with iron oxide nanoparticles, the generation of cell-agarose constructs and implantation of these constructs into cartilage defects. The labeled constructs can be tracked non-invasively with MR-Imaging. |
format | Text |
id | pubmed-2900275 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | MyJove Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-29002752011-04-05 Implantation of Ferumoxides Labeled Human Mesenchymal Stem Cells in Cartilage Defects Nedopil, Alexander J. Mandrussow, Lydia G. Daldrup-Link, Heike E. J Vis Exp Cellular Biology The field of tissue engineering integrates the principles of engineering, cell biology and medicine towards the regeneration of specific cells and functional tissue. Matrix associated stem cell implants (MASI) aim to regenerate cartilage defects due to arthritic or traumatic joint injuries. Adult mesenchymal stem cells (MSCs) have the ability to differentiate into cells of the chondrogenic lineage and have shown promising results for cell-based articular cartilage repair technologies. Autologous MSCs can be isolated from a variety of tissues, can be expanded in cell cultures without losing their differentiation potential, and have demonstrated chondrogenic differentiation in vitro and in vivo(1, 2). In order to provide local retention and viability of transplanted MSCs in cartilage defects, a scaffold is needed, which also supports subsequent differentiation and proliferation. The architecture of the scaffold guides tissue formation and permits the extracellular matrix, produced by the stem cells, to expand. Previous investigations have shown that a 2% agarose scaffold may support the development of stable hyaline cartilage and does not induce immune responses(3). Long term retention of transplanted stem cells in MASI is critical for cartilage regeneration. Labeling of MSCs with iron oxide nanoparticles allows for long-term in vivo tracking with non-invasive MR imaging techniques(4). This presentation will demonstrate techniques for labeling MSCs with iron oxide nanoparticles, the generation of cell-agarose constructs and implantation of these constructs into cartilage defects. The labeled constructs can be tracked non-invasively with MR-Imaging. MyJove Corporation 2010-04-05 /pmc/articles/PMC2900275/ /pubmed/20368696 http://dx.doi.org/10.3791/1793 Text en Copyright © 2010, Journal of Visualized Experiments http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Cellular Biology Nedopil, Alexander J. Mandrussow, Lydia G. Daldrup-Link, Heike E. Implantation of Ferumoxides Labeled Human Mesenchymal Stem Cells in Cartilage Defects |
title | Implantation of Ferumoxides Labeled Human Mesenchymal Stem Cells in Cartilage Defects |
title_full | Implantation of Ferumoxides Labeled Human Mesenchymal Stem Cells in Cartilage Defects |
title_fullStr | Implantation of Ferumoxides Labeled Human Mesenchymal Stem Cells in Cartilage Defects |
title_full_unstemmed | Implantation of Ferumoxides Labeled Human Mesenchymal Stem Cells in Cartilage Defects |
title_short | Implantation of Ferumoxides Labeled Human Mesenchymal Stem Cells in Cartilage Defects |
title_sort | implantation of ferumoxides labeled human mesenchymal stem cells in cartilage defects |
topic | Cellular Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2900275/ https://www.ncbi.nlm.nih.gov/pubmed/20368696 http://dx.doi.org/10.3791/1793 |
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