Tracking the fate of stem cell implants with fluorine-19 MRI.

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

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Main Authors: Jeffrey M Gaudet, Emeline J Ribot, Yuhua Chen, Kyle M Gilbert, Paula J Foster
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4358825?pdf=render
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spelling doaj-7b7b2bcc691246ca9df005e15b00e7d42020-11-24T22:15:44ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01103e011854410.1371/journal.pone.0118544Tracking the fate of stem cell implants with fluorine-19 MRI.Jeffrey M GaudetEmeline J RibotYuhua ChenKyle M GilbertPaula J FosterIn this study we used cellular magnetic resonance imaging (MRI) to detect mesenchymal stem cells (MSC) labeled with a Fluorine-19 (19F) agent. 19F-MRI offers unambiguous detection and in vivo quantification of labeled cells.We investigated two common stem cell transplant mouse models: an immune competent, syngeneic transplant model and an immune compromised, xenograft transplant model. 19F labelled stem cells were implanted intramuscularly into the hindlimb of healthy mice. The transplant was then monitored for up to 17 days using 19F-MRI, after which the tissue was excised for fluorescence microscopy and immunohistochemisty.Immediately following transplantation, 19F-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 19F signal. In the xenograft model, all mice had detectable signal at endpoint. Fluorescence microscopy and immunohistochemistry were used to show that the 19F signal was related to the presence of bystander labeled macrophages, and not original MSC.Our results show that 19F-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.http://europepmc.org/articles/PMC4358825?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Jeffrey M Gaudet
Emeline J Ribot
Yuhua Chen
Kyle M Gilbert
Paula J Foster
spellingShingle Jeffrey M Gaudet
Emeline J Ribot
Yuhua Chen
Kyle M Gilbert
Paula J Foster
Tracking the fate of stem cell implants with fluorine-19 MRI.
PLoS ONE
author_facet Jeffrey M Gaudet
Emeline J Ribot
Yuhua Chen
Kyle M Gilbert
Paula J Foster
author_sort Jeffrey M Gaudet
title 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_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_sort tracking the fate of stem cell implants with fluorine-19 mri.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2015-01-01
description In this study we used cellular magnetic resonance imaging (MRI) to detect mesenchymal stem cells (MSC) labeled with a Fluorine-19 (19F) agent. 19F-MRI offers unambiguous detection and in vivo quantification of labeled cells.We investigated two common stem cell transplant mouse models: an immune competent, syngeneic transplant model and an immune compromised, xenograft transplant model. 19F labelled stem cells were implanted intramuscularly into the hindlimb of healthy mice. The transplant was then monitored for up to 17 days using 19F-MRI, after which the tissue was excised for fluorescence microscopy and immunohistochemisty.Immediately following transplantation, 19F-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 19F signal. In the xenograft model, all mice had detectable signal at endpoint. Fluorescence microscopy and immunohistochemistry were used to show that the 19F signal was related to the presence of bystander labeled macrophages, and not original MSC.Our results show that 19F-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.
url http://europepmc.org/articles/PMC4358825?pdf=render
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