Cargando…

Tracking the Fate of Stem Cell Implants with Fluorine-19 MRI

BACKGROUND: In this study we used cellular magnetic resonance imaging (MRI) to detect mesenchymal stem cells (MSC) labeled with a Fluorine-19 ((19)F) agent. (19)F-MRI offers unambiguous detection and in vivo quantification of labeled cells. METHODS: We investigated two common stem cell transplant mo...

Descripción completa

Detalles Bibliográficos
Autores principales: Gaudet, Jeffrey M., Ribot, Emeline J., Chen, Yuhua, Gilbert, Kyle M., Foster, Paula J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4358825/
https://www.ncbi.nlm.nih.gov/pubmed/25767871
http://dx.doi.org/10.1371/journal.pone.0118544
_version_ 1782361290645176320
author Gaudet, Jeffrey M.
Ribot, Emeline J.
Chen, Yuhua
Gilbert, Kyle M.
Foster, Paula J.
author_facet Gaudet, Jeffrey M.
Ribot, Emeline J.
Chen, Yuhua
Gilbert, Kyle M.
Foster, Paula J.
author_sort Gaudet, Jeffrey M.
collection PubMed
description BACKGROUND: In this study we used cellular magnetic resonance imaging (MRI) to detect mesenchymal stem cells (MSC) labeled with a Fluorine-19 ((19)F) agent. (19)F-MRI offers unambiguous detection and in vivo quantification of labeled cells. METHODS: We investigated two common stem cell transplant mouse models: an immune competent, syngeneic transplant model and an immune compromised, xenograft transplant model. (19)F labelled stem cells were implanted intramuscularly into the hindlimb of healthy mice. The transplant was then monitored for up to 17 days using (19)F-MRI, after which the tissue was excised for fluorescence microscopy and immunohistochemisty. RESULTS: Immediately following transplantation, (19)F-MRI quantification correlated very well with the expected cell number in both models. The 19F signal decreased over time in both models, with a more rapid decrease in the syngeneic model. By endpoint, only 2/7 syngeneic mice had any detectable (19)F signal. In the xenograft model, all mice had detectable signal at endpoint. Fluorescence microscopy and immunohistochemistry were used to show that the (19)F signal was related to the presence of bystander labeled macrophages, and not original MSC. CONCLUSIONS: Our results show that (19)F-MRI is an excellent tool for verifying the delivery of therapeutic cells early after transplantation. However, in certain circumstances the transfer of cellular label to other bystander cells may confuse interpretation of the long-term fate of the transplanted cells.
format Online
Article
Text
id pubmed-4358825
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-43588252015-03-23 Tracking the Fate of Stem Cell Implants with Fluorine-19 MRI Gaudet, Jeffrey M. Ribot, Emeline J. Chen, Yuhua Gilbert, Kyle M. Foster, Paula J. PLoS One Research Article BACKGROUND: In this study we used cellular magnetic resonance imaging (MRI) to detect mesenchymal stem cells (MSC) labeled with a Fluorine-19 ((19)F) agent. (19)F-MRI offers unambiguous detection and in vivo quantification of labeled cells. METHODS: We investigated two common stem cell transplant mouse models: an immune competent, syngeneic transplant model and an immune compromised, xenograft transplant model. (19)F labelled stem cells were implanted intramuscularly into the hindlimb of healthy mice. The transplant was then monitored for up to 17 days using (19)F-MRI, after which the tissue was excised for fluorescence microscopy and immunohistochemisty. RESULTS: Immediately following transplantation, (19)F-MRI quantification correlated very well with the expected cell number in both models. The 19F signal decreased over time in both models, with a more rapid decrease in the syngeneic model. By endpoint, only 2/7 syngeneic mice had any detectable (19)F signal. In the xenograft model, all mice had detectable signal at endpoint. Fluorescence microscopy and immunohistochemistry were used to show that the (19)F signal was related to the presence of bystander labeled macrophages, and not original MSC. CONCLUSIONS: Our results show that (19)F-MRI is an excellent tool for verifying the delivery of therapeutic cells early after transplantation. However, in certain circumstances the transfer of cellular label to other bystander cells may confuse interpretation of the long-term fate of the transplanted cells. Public Library of Science 2015-03-13 /pmc/articles/PMC4358825/ /pubmed/25767871 http://dx.doi.org/10.1371/journal.pone.0118544 Text en © 2015 Gaudet et al http://creativecommons.org/licenses/by/4.0/ 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 author and source are properly credited.
spellingShingle Research Article
Gaudet, Jeffrey M.
Ribot, Emeline J.
Chen, Yuhua
Gilbert, Kyle M.
Foster, Paula J.
Tracking the Fate of Stem Cell Implants with Fluorine-19 MRI
title Tracking the Fate of Stem Cell Implants with Fluorine-19 MRI
title_full Tracking the Fate of Stem Cell Implants with Fluorine-19 MRI
title_fullStr Tracking the Fate of Stem Cell Implants with Fluorine-19 MRI
title_full_unstemmed Tracking the Fate of Stem Cell Implants with Fluorine-19 MRI
title_short Tracking the Fate of Stem Cell Implants with Fluorine-19 MRI
title_sort tracking the fate of stem cell implants with fluorine-19 mri
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4358825/
https://www.ncbi.nlm.nih.gov/pubmed/25767871
http://dx.doi.org/10.1371/journal.pone.0118544
work_keys_str_mv AT gaudetjeffreym trackingthefateofstemcellimplantswithfluorine19mri
AT ribotemelinej trackingthefateofstemcellimplantswithfluorine19mri
AT chenyuhua trackingthefateofstemcellimplantswithfluorine19mri
AT gilbertkylem trackingthefateofstemcellimplantswithfluorine19mri
AT fosterpaulaj trackingthefateofstemcellimplantswithfluorine19mri