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In vivo distribution of U87MG cells injected into the lateral ventricle of rats with spinal cord injury

Stem cells could be the next generation therapeutic option for neurodegenerative diseases including spinal cord injury (SCI). However, several critical factors such as delivery method should be determined before their clinical applications. Previously, we have demonstrated that lateral ventricle (LV...

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Autores principales: Won, Jeong-Seob, Nam, Hyun, Lee, Hye Won, Hwang, Ji-Yoon, Noh, Yu-Jeong, Nam, Do-Hyun, Lee, Sun-Ho, Joo, Kyeung Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6095526/
https://www.ncbi.nlm.nih.gov/pubmed/30114270
http://dx.doi.org/10.1371/journal.pone.0202307
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author Won, Jeong-Seob
Nam, Hyun
Lee, Hye Won
Hwang, Ji-Yoon
Noh, Yu-Jeong
Nam, Do-Hyun
Lee, Sun-Ho
Joo, Kyeung Min
author_facet Won, Jeong-Seob
Nam, Hyun
Lee, Hye Won
Hwang, Ji-Yoon
Noh, Yu-Jeong
Nam, Do-Hyun
Lee, Sun-Ho
Joo, Kyeung Min
author_sort Won, Jeong-Seob
collection PubMed
description Stem cells could be the next generation therapeutic option for neurodegenerative diseases including spinal cord injury (SCI). However, several critical factors such as delivery method should be determined before their clinical applications. Previously, we have demonstrated that lateral ventricle (LV) injection as preclinical simulation could be used for intrathecal administration in clinical trials using rodent animal models. In this study, we further analyzed in vivo distribution of cells that were injected into LVs of rats with SCI at thoracic level using in vivo imaging techniques. When 5 × 10(6) U87MG cells labelled with fluorescent magnetic nanoparticle (FMNP-labelled U87MG) were administrated into LVs at 7 days after SCI, FMNP-labelled U87MG cells were observed in all regions of the spinal cord at 24 hours after the injection. Compared to water-soluble Cy5.5 fluorescent dye or rats without SCI, in vivo distribution pattern of FMNP-labelled U87MG cells was not different, although migration to the spinal cord was significantly reduced in both Cy5.5 fluorescent dye and FMNP-labelled U87MG cells caused by the injury. The presence of FMNP-labelled U87MG cells in the spinal cord was confirmed by quantitative PCR for human specific sequence and immunohistochemistry staining using antibody against human specific antigen. These data indicate that LV injection could recapitulate intrathecal administration of stem cells for SCI patients. Results of this study might be applied further to the planning of optimal preclinical and clinical trials of stem cell therapeutics for SCI.
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spelling pubmed-60955262018-08-30 In vivo distribution of U87MG cells injected into the lateral ventricle of rats with spinal cord injury Won, Jeong-Seob Nam, Hyun Lee, Hye Won Hwang, Ji-Yoon Noh, Yu-Jeong Nam, Do-Hyun Lee, Sun-Ho Joo, Kyeung Min PLoS One Research Article Stem cells could be the next generation therapeutic option for neurodegenerative diseases including spinal cord injury (SCI). However, several critical factors such as delivery method should be determined before their clinical applications. Previously, we have demonstrated that lateral ventricle (LV) injection as preclinical simulation could be used for intrathecal administration in clinical trials using rodent animal models. In this study, we further analyzed in vivo distribution of cells that were injected into LVs of rats with SCI at thoracic level using in vivo imaging techniques. When 5 × 10(6) U87MG cells labelled with fluorescent magnetic nanoparticle (FMNP-labelled U87MG) were administrated into LVs at 7 days after SCI, FMNP-labelled U87MG cells were observed in all regions of the spinal cord at 24 hours after the injection. Compared to water-soluble Cy5.5 fluorescent dye or rats without SCI, in vivo distribution pattern of FMNP-labelled U87MG cells was not different, although migration to the spinal cord was significantly reduced in both Cy5.5 fluorescent dye and FMNP-labelled U87MG cells caused by the injury. The presence of FMNP-labelled U87MG cells in the spinal cord was confirmed by quantitative PCR for human specific sequence and immunohistochemistry staining using antibody against human specific antigen. These data indicate that LV injection could recapitulate intrathecal administration of stem cells for SCI patients. Results of this study might be applied further to the planning of optimal preclinical and clinical trials of stem cell therapeutics for SCI. Public Library of Science 2018-08-16 /pmc/articles/PMC6095526/ /pubmed/30114270 http://dx.doi.org/10.1371/journal.pone.0202307 Text en © 2018 Won 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Won, Jeong-Seob
Nam, Hyun
Lee, Hye Won
Hwang, Ji-Yoon
Noh, Yu-Jeong
Nam, Do-Hyun
Lee, Sun-Ho
Joo, Kyeung Min
In vivo distribution of U87MG cells injected into the lateral ventricle of rats with spinal cord injury
title In vivo distribution of U87MG cells injected into the lateral ventricle of rats with spinal cord injury
title_full In vivo distribution of U87MG cells injected into the lateral ventricle of rats with spinal cord injury
title_fullStr In vivo distribution of U87MG cells injected into the lateral ventricle of rats with spinal cord injury
title_full_unstemmed In vivo distribution of U87MG cells injected into the lateral ventricle of rats with spinal cord injury
title_short In vivo distribution of U87MG cells injected into the lateral ventricle of rats with spinal cord injury
title_sort in vivo distribution of u87mg cells injected into the lateral ventricle of rats with spinal cord injury
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6095526/
https://www.ncbi.nlm.nih.gov/pubmed/30114270
http://dx.doi.org/10.1371/journal.pone.0202307
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