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Ferumoxytol Labeling of Human Neural Progenitor Cells for Diagnostic Cellular Tracking in the Porcine Spinal Cord with Magnetic Resonance Imaging

We report on the diagnostic capability of magnetic resonance imaging (MRI)‐based tracking of ferumoxytol‐labeled human neural progenitor cells (hNPCs) transplanted into the porcine spinal cord. hNPCs prelabeled with two doses of ferumoxytol nanoparticles (hNPC‐F(Low) and hNPC‐F(High)) were injected...

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Autores principales: Lamanna, Jason J., Gutierrez, Juanmarco, Urquia, Lindsey N., Hurtig, C. Victor, Amador, Elman, Grin, Natalia, Svendsen, Clive N., Federici, Thais, Oshinski, John N., Boulis, Nicholas M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5442757/
https://www.ncbi.nlm.nih.gov/pubmed/28170192
http://dx.doi.org/10.5966/sctm.2015-0422
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author Lamanna, Jason J.
Gutierrez, Juanmarco
Urquia, Lindsey N.
Hurtig, C. Victor
Amador, Elman
Grin, Natalia
Svendsen, Clive N.
Federici, Thais
Oshinski, John N.
Boulis, Nicholas M.
author_facet Lamanna, Jason J.
Gutierrez, Juanmarco
Urquia, Lindsey N.
Hurtig, C. Victor
Amador, Elman
Grin, Natalia
Svendsen, Clive N.
Federici, Thais
Oshinski, John N.
Boulis, Nicholas M.
author_sort Lamanna, Jason J.
collection PubMed
description We report on the diagnostic capability of magnetic resonance imaging (MRI)‐based tracking of ferumoxytol‐labeled human neural progenitor cells (hNPCs) transplanted into the porcine spinal cord. hNPCs prelabeled with two doses of ferumoxytol nanoparticles (hNPC‐F(Low) and hNPC‐F(High)) were injected into the ventral horn of the spinal cord in healthy minipigs. Ferumoxytol‐labeled grafts were tracked in vivo up to 105 days after transplantation with MRI. Injection accuracy was assessed in vivo at day 14 and was predictive of “on” or “off” target cell graft location assessed by histology. No difference in long‐term cell survival, assessed by quantitative stereology, was observed among hNPC‐F(Low), hNPC‐F(High), or control grafts. Histological iron colocalized with MRI signal and engrafted human nuclei. Furthermore, the ferumoxytol‐labeled cells retained nanoparticles and function in vivo. This approach represents an important leap forward toward facilitating translation of cell‐tracking technologies to clinical trials by providing a method of assessing transplantation accuracy, delivered dose, and potentially cell survival. Stem Cells Translational Medicine 2017;6:139–150
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spelling pubmed-54427572017-06-15 Ferumoxytol Labeling of Human Neural Progenitor Cells for Diagnostic Cellular Tracking in the Porcine Spinal Cord with Magnetic Resonance Imaging Lamanna, Jason J. Gutierrez, Juanmarco Urquia, Lindsey N. Hurtig, C. Victor Amador, Elman Grin, Natalia Svendsen, Clive N. Federici, Thais Oshinski, John N. Boulis, Nicholas M. Stem Cells Transl Med Translational Research Articles and Reviews We report on the diagnostic capability of magnetic resonance imaging (MRI)‐based tracking of ferumoxytol‐labeled human neural progenitor cells (hNPCs) transplanted into the porcine spinal cord. hNPCs prelabeled with two doses of ferumoxytol nanoparticles (hNPC‐F(Low) and hNPC‐F(High)) were injected into the ventral horn of the spinal cord in healthy minipigs. Ferumoxytol‐labeled grafts were tracked in vivo up to 105 days after transplantation with MRI. Injection accuracy was assessed in vivo at day 14 and was predictive of “on” or “off” target cell graft location assessed by histology. No difference in long‐term cell survival, assessed by quantitative stereology, was observed among hNPC‐F(Low), hNPC‐F(High), or control grafts. Histological iron colocalized with MRI signal and engrafted human nuclei. Furthermore, the ferumoxytol‐labeled cells retained nanoparticles and function in vivo. This approach represents an important leap forward toward facilitating translation of cell‐tracking technologies to clinical trials by providing a method of assessing transplantation accuracy, delivered dose, and potentially cell survival. Stem Cells Translational Medicine 2017;6:139–150 John Wiley and Sons Inc. 2016-08-29 2017-01 /pmc/articles/PMC5442757/ /pubmed/28170192 http://dx.doi.org/10.5966/sctm.2015-0422 Text en © 2016 The Authors Stem Cells Translational Medicine published by Wiley Periodicals, Inc. on behalf of AlphaMed Press This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Translational Research Articles and Reviews
Lamanna, Jason J.
Gutierrez, Juanmarco
Urquia, Lindsey N.
Hurtig, C. Victor
Amador, Elman
Grin, Natalia
Svendsen, Clive N.
Federici, Thais
Oshinski, John N.
Boulis, Nicholas M.
Ferumoxytol Labeling of Human Neural Progenitor Cells for Diagnostic Cellular Tracking in the Porcine Spinal Cord with Magnetic Resonance Imaging
title Ferumoxytol Labeling of Human Neural Progenitor Cells for Diagnostic Cellular Tracking in the Porcine Spinal Cord with Magnetic Resonance Imaging
title_full Ferumoxytol Labeling of Human Neural Progenitor Cells for Diagnostic Cellular Tracking in the Porcine Spinal Cord with Magnetic Resonance Imaging
title_fullStr Ferumoxytol Labeling of Human Neural Progenitor Cells for Diagnostic Cellular Tracking in the Porcine Spinal Cord with Magnetic Resonance Imaging
title_full_unstemmed Ferumoxytol Labeling of Human Neural Progenitor Cells for Diagnostic Cellular Tracking in the Porcine Spinal Cord with Magnetic Resonance Imaging
title_short Ferumoxytol Labeling of Human Neural Progenitor Cells for Diagnostic Cellular Tracking in the Porcine Spinal Cord with Magnetic Resonance Imaging
title_sort ferumoxytol labeling of human neural progenitor cells for diagnostic cellular tracking in the porcine spinal cord with magnetic resonance imaging
topic Translational Research Articles and Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5442757/
https://www.ncbi.nlm.nih.gov/pubmed/28170192
http://dx.doi.org/10.5966/sctm.2015-0422
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