Survival of Neural Progenitors Allografted into the CNS of Immunocompetent Recipients is Highly Dependent on Transplantation Site

Allografts continue to be used in clinical neurotransplantation studies; hence, it is crucial to understand the mechanisms that govern allograft tolerance. We investigated the impact of transplantation site within the brain on graft survival. Mouse [Friend leukemia virus, strain B (FVB)] glial precu...

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Main Authors: M. Janowski, C. Engels, M. Gorelik, A. Lyczek, S. Bernard, J. W. M. Bulte, P. Walczak M.D.
Format: Article
Language:English
Published: SAGE Publishing 2014-03-01
Series:Cell Transplantation
Online Access:https://doi.org/10.3727/096368912X661328
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spelling doaj-c228bee440ea4fe4a597eb71cc2f1b1d2020-11-25T03:24:16ZengSAGE PublishingCell Transplantation0963-68971555-38922014-03-012310.3727/096368912X661328Survival of Neural Progenitors Allografted into the CNS of Immunocompetent Recipients is Highly Dependent on Transplantation SiteM. Janowski0C. Engels1M. Gorelik2A. Lyczek3S. Bernard4J. W. M. Bulte5P. Walczak M.D.6Department of Neurosurgery, Mossakowski Medical Research Centre, Polish Academy of Sciences, Warsaw, PolandCellular Imaging Section and Vascular Biology Program, Institute for Cell Engineering, The Johns Hopkins University School of Medicine, Baltimore, MD, USACellular Imaging Section and Vascular Biology Program, Institute for Cell Engineering, The Johns Hopkins University School of Medicine, Baltimore, MD, USACellular Imaging Section and Vascular Biology Program, Institute for Cell Engineering, The Johns Hopkins University School of Medicine, Baltimore, MD, USACellular Imaging Section and Vascular Biology Program, Institute for Cell Engineering, The Johns Hopkins University School of Medicine, Baltimore, MD, USADepartment of Oncology, The Johns Hopkins University School of Medicine, Baltimore, MD, USADepartment of Radiology, Faculty of Medical Sciences, University of Warmia and Mazury, Olsztyn, PolandAllografts continue to be used in clinical neurotransplantation studies; hence, it is crucial to understand the mechanisms that govern allograft tolerance. We investigated the impact of transplantation site within the brain on graft survival. Mouse [Friend leukemia virus, strain B (FVB)] glial precursors, transfected with luciferase, were injected (3 × 10 5 ) into the forceps minor (FM) or striatum (STR). Immunodeficient rag2 −/- and immuno-competent BALB/c mice were used as recipients. Magnetic resonance imaging (MRI) confirmed that cells were precisely deposited at the selected coordinates. The graft viability was assessed noninvasively with biolumi-nescent imaging (BLI) for a period of 16 days. Regardless of implantation site, all grafts ( n = 10) deposited in immunodeficient animals revealed excellent survival. In contrast, immunocompetent animals only accepted grafts at the STR site ( n = 10), whereas all the FM grafts were rejected ( n = 10). To investigate the factors that led to rejection of FM grafts, with acceptance of STR grafts, another group of animals ( n = 19) was sacrificed during the prerejection period, on day 5. Near-infrared fluorescence imaging with IRDye 800CW–polyethylene glycol probe displayed similar blood–brain barrier disruption at both graft locations. The morphological distribution of FM grafts was cylindrical, parallel to the needle track, whereas cells transplanted into the STR accumulated along the border between the STR and the corpus callosum. There was significantly less infiltration by both innate and adaptive immune cells in the STR grafts, especially along the calloso-striatal border. With allograft survival being dependent on the transplantation site, the anatomical coordinates of the graft target should always be taken into account as it may determine the success or failure of therapy.https://doi.org/10.3727/096368912X661328
collection DOAJ
language English
format Article
sources DOAJ
author M. Janowski
C. Engels
M. Gorelik
A. Lyczek
S. Bernard
J. W. M. Bulte
P. Walczak M.D.
spellingShingle M. Janowski
C. Engels
M. Gorelik
A. Lyczek
S. Bernard
J. W. M. Bulte
P. Walczak M.D.
Survival of Neural Progenitors Allografted into the CNS of Immunocompetent Recipients is Highly Dependent on Transplantation Site
Cell Transplantation
author_facet M. Janowski
C. Engels
M. Gorelik
A. Lyczek
S. Bernard
J. W. M. Bulte
P. Walczak M.D.
author_sort M. Janowski
title Survival of Neural Progenitors Allografted into the CNS of Immunocompetent Recipients is Highly Dependent on Transplantation Site
title_short Survival of Neural Progenitors Allografted into the CNS of Immunocompetent Recipients is Highly Dependent on Transplantation Site
title_full Survival of Neural Progenitors Allografted into the CNS of Immunocompetent Recipients is Highly Dependent on Transplantation Site
title_fullStr Survival of Neural Progenitors Allografted into the CNS of Immunocompetent Recipients is Highly Dependent on Transplantation Site
title_full_unstemmed Survival of Neural Progenitors Allografted into the CNS of Immunocompetent Recipients is Highly Dependent on Transplantation Site
title_sort survival of neural progenitors allografted into the cns of immunocompetent recipients is highly dependent on transplantation site
publisher SAGE Publishing
series Cell Transplantation
issn 0963-6897
1555-3892
publishDate 2014-03-01
description Allografts continue to be used in clinical neurotransplantation studies; hence, it is crucial to understand the mechanisms that govern allograft tolerance. We investigated the impact of transplantation site within the brain on graft survival. Mouse [Friend leukemia virus, strain B (FVB)] glial precursors, transfected with luciferase, were injected (3 × 10 5 ) into the forceps minor (FM) or striatum (STR). Immunodeficient rag2 −/- and immuno-competent BALB/c mice were used as recipients. Magnetic resonance imaging (MRI) confirmed that cells were precisely deposited at the selected coordinates. The graft viability was assessed noninvasively with biolumi-nescent imaging (BLI) for a period of 16 days. Regardless of implantation site, all grafts ( n = 10) deposited in immunodeficient animals revealed excellent survival. In contrast, immunocompetent animals only accepted grafts at the STR site ( n = 10), whereas all the FM grafts were rejected ( n = 10). To investigate the factors that led to rejection of FM grafts, with acceptance of STR grafts, another group of animals ( n = 19) was sacrificed during the prerejection period, on day 5. Near-infrared fluorescence imaging with IRDye 800CW–polyethylene glycol probe displayed similar blood–brain barrier disruption at both graft locations. The morphological distribution of FM grafts was cylindrical, parallel to the needle track, whereas cells transplanted into the STR accumulated along the border between the STR and the corpus callosum. There was significantly less infiltration by both innate and adaptive immune cells in the STR grafts, especially along the calloso-striatal border. With allograft survival being dependent on the transplantation site, the anatomical coordinates of the graft target should always be taken into account as it may determine the success or failure of therapy.
url https://doi.org/10.3727/096368912X661328
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