Tracking mesenchymal stem cells using magnetic resonance imaging

Recent translational studies in the fields of tissue regeneration and cell therapy have characterized mesenchymal stem cells (MSCs) as a potentially effective and accessible measure for treating ischemic cerebral and neurodegenerative disorders such as stroke, Parkinson's disease, and amyotroph...

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Main Authors: Jens T Rosenberg, Xuegang Yuan, Samuel Grant, Teng Ma
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2016-01-01
Series:Brain Circulation
Subjects:
Online Access:http://www.braincirculation.org/article.asp?issn=2394-8108;year=2016;volume=2;issue=3;spage=108;epage=113;aulast=Rosenberg
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spelling doaj-7f5473622a2244898f096012e56fef382020-11-24T23:37:03ZengWolters Kluwer Medknow PublicationsBrain Circulation2455-46262016-01-012310811310.4103/2394-8108.192521Tracking mesenchymal stem cells using magnetic resonance imagingJens T RosenbergXuegang YuanSamuel GrantTeng MaRecent translational studies in the fields of tissue regeneration and cell therapy have characterized mesenchymal stem cells (MSCs) as a potentially effective and accessible measure for treating ischemic cerebral and neurodegenerative disorders such as stroke, Parkinson's disease, and amyotrophic lateral sclerosis. Developing more efficient cell tracking techniques bear the potential to optimize MSC transplantation therapies by providing a more accurate picture of the fate and area of effect of implanted cells. Currently, determining the location of transplanted MSCs involves a histological approach, but magnetic resonance imaging (MRI) presents a noninvasive paradigm that permits repeat evaluations. To visualize MSCs using MRI, the implanted cells must be treated with an intracellular contrast agent. These are commonly paramagnetic compounds, many of which are based on superparamagnetic iron oxide (SPIO) nanoparticles. Recent research has set out characterize the effects of SPIO-uptake on the cellular activity of in vitro human MSCs and the resultant influence that respective SPIO concentration has on MRI sensitivity. As these studies reveal, SPIO-uptake has no effect on the cellular processes of proliferation and differentiation while producing high contrast MRI signals. Moreover, transplantation of SPIO-labeled MSCs in animal models encouragingly showed no loss in MRI contrast, suggesting that SPIO labeling may be an appealing regime for lasting MRI detection. This study is a review article. Referred literature in this study has been listed in the reference part. The datasets supporting the conclusions of this article are available online by searching the PubMed. Some original points in this article come from the laboratory practice in our research centers and the authors' experiences.http://www.braincirculation.org/article.asp?issn=2394-8108;year=2016;volume=2;issue=3;spage=108;epage=113;aulast=RosenbergCell trackinghuman mesenchymal stem cellshypoxiaischemiamagnetic resonance imagingsuperparamagnetic iron oxide
collection DOAJ
language English
format Article
sources DOAJ
author Jens T Rosenberg
Xuegang Yuan
Samuel Grant
Teng Ma
spellingShingle Jens T Rosenberg
Xuegang Yuan
Samuel Grant
Teng Ma
Tracking mesenchymal stem cells using magnetic resonance imaging
Brain Circulation
Cell tracking
human mesenchymal stem cells
hypoxia
ischemia
magnetic resonance imaging
superparamagnetic iron oxide
author_facet Jens T Rosenberg
Xuegang Yuan
Samuel Grant
Teng Ma
author_sort Jens T Rosenberg
title Tracking mesenchymal stem cells using magnetic resonance imaging
title_short Tracking mesenchymal stem cells using magnetic resonance imaging
title_full Tracking mesenchymal stem cells using magnetic resonance imaging
title_fullStr Tracking mesenchymal stem cells using magnetic resonance imaging
title_full_unstemmed Tracking mesenchymal stem cells using magnetic resonance imaging
title_sort tracking mesenchymal stem cells using magnetic resonance imaging
publisher Wolters Kluwer Medknow Publications
series Brain Circulation
issn 2455-4626
publishDate 2016-01-01
description Recent translational studies in the fields of tissue regeneration and cell therapy have characterized mesenchymal stem cells (MSCs) as a potentially effective and accessible measure for treating ischemic cerebral and neurodegenerative disorders such as stroke, Parkinson's disease, and amyotrophic lateral sclerosis. Developing more efficient cell tracking techniques bear the potential to optimize MSC transplantation therapies by providing a more accurate picture of the fate and area of effect of implanted cells. Currently, determining the location of transplanted MSCs involves a histological approach, but magnetic resonance imaging (MRI) presents a noninvasive paradigm that permits repeat evaluations. To visualize MSCs using MRI, the implanted cells must be treated with an intracellular contrast agent. These are commonly paramagnetic compounds, many of which are based on superparamagnetic iron oxide (SPIO) nanoparticles. Recent research has set out characterize the effects of SPIO-uptake on the cellular activity of in vitro human MSCs and the resultant influence that respective SPIO concentration has on MRI sensitivity. As these studies reveal, SPIO-uptake has no effect on the cellular processes of proliferation and differentiation while producing high contrast MRI signals. Moreover, transplantation of SPIO-labeled MSCs in animal models encouragingly showed no loss in MRI contrast, suggesting that SPIO labeling may be an appealing regime for lasting MRI detection. This study is a review article. Referred literature in this study has been listed in the reference part. The datasets supporting the conclusions of this article are available online by searching the PubMed. Some original points in this article come from the laboratory practice in our research centers and the authors' experiences.
topic Cell tracking
human mesenchymal stem cells
hypoxia
ischemia
magnetic resonance imaging
superparamagnetic iron oxide
url http://www.braincirculation.org/article.asp?issn=2394-8108;year=2016;volume=2;issue=3;spage=108;epage=113;aulast=Rosenberg
work_keys_str_mv AT jenstrosenberg trackingmesenchymalstemcellsusingmagneticresonanceimaging
AT xuegangyuan trackingmesenchymalstemcellsusingmagneticresonanceimaging
AT samuelgrant trackingmesenchymalstemcellsusingmagneticresonanceimaging
AT tengma trackingmesenchymalstemcellsusingmagneticresonanceimaging
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