Comparative Study of Methods for Administering Neural Stem/Progenitor Cells to Treat Spinal Cord Injury in Mice

To investigate potential cures for spinal cord injury (SCI), several researchers have transplanted neural stem/progenitor cells (NS/PCs) into the injured spinal cord by different procedures, including intralesional (IL), intrathecal (IT), and intravenous (IV) injection. However, there are no reports...

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Main Authors: Yuichiro Takahashi, Osahiko Tsuji, Gentaro Kumagai, Chikako Miyauchi Hara, Hirotaka James Okano, Atsushi Miyawaki, Yoshiaki Toyama, Hideyuki Okano, Masaya Nakamura
Format: Article
Language:English
Published: SAGE Publishing 2011-06-01
Series:Cell Transplantation
Online Access:https://doi.org/10.3727/096368910X536554
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spelling doaj-98ae9c2640ea4b419932ebace1134dd82020-11-25T03:39:23ZengSAGE PublishingCell Transplantation0963-68971555-38922011-06-012010.3727/096368910X536554Comparative Study of Methods for Administering Neural Stem/Progenitor Cells to Treat Spinal Cord Injury in MiceYuichiro Takahashi0Osahiko Tsuji1Gentaro Kumagai2Chikako Miyauchi Hara3Hirotaka James Okano4Atsushi Miyawaki5Yoshiaki Toyama6Hideyuki Okano7Masaya Nakamura8Department of Physiology, School of Medicine, Keio University, Tokyo, JapanDepartment of Orthopaedic Surgery, School of Medicine, Keio University, Tokyo, JapanDepartment of Orthopaedic Surgery, School of Medicine, Hirosaki University, Aomori, JapanDepartment of Physiology, School of Medicine, Keio University, Tokyo, JapanDepartment of Physiology, School of Medicine, Keio University, Tokyo, JapanLife Function and Dynamics, ERATO, JST, Saitama, JapanDepartment of Orthopaedic Surgery, School of Medicine, Keio University, Tokyo, JapanDepartment of Physiology, School of Medicine, Keio University, Tokyo, JapanDepartment of Orthopaedic Surgery, School of Medicine, Keio University, Tokyo, JapanTo investigate potential cures for spinal cord injury (SCI), several researchers have transplanted neural stem/progenitor cells (NS/PCs) into the injured spinal cord by different procedures, including intralesional (IL), intrathecal (IT), and intravenous (IV) injection. However, there are no reports quantifying or comparing the number of cells successfully transplanted to the lesion site by each procedure in vivo. The purpose of the present study was to determine the optimal method of cell transplantation to the SCI site in terms of grafted cell survival and safety. For this purpose, we developed mouse NS/PCs that expressed a novel Venus-luciferase fusion protein that enabled us to detect a minimum of 1,000 grafted cells in vivo by bioluminescence imaging (BLI). After inducing contusive SCI at the T10 level in mice, NS/PCs were transplanted into the injured animals three different ways: by IL, IT, or IV injection. Six weeks after the transplantation, BLI analysis showed that in the IL group, the luminescence intensity of the grafted cells had decreased to about 10% of its initial level, and appeared at the site of injury. In the IT group, the luminescence of the grafted cells, which was distributed throughout the entire subarachnoid space immediately after transplantation, was detected at the injured site 1 week later, and by 6 weeks had gradually decreased to about 0.3% of its initial level. In the IV group, no grafted cells were detected at the site of injury, but all of these mice showed luminescence in the bilateral chest, suggesting pulmonary embolism. In addition, one third of these mice died immediately after the IV injection. In terms of grafted cell survival and safety, we conclude that the IL application of NS/PCs is the most effective and feasible method for transplanting NS/PCs into the SCI site.https://doi.org/10.3727/096368910X536554
collection DOAJ
language English
format Article
sources DOAJ
author Yuichiro Takahashi
Osahiko Tsuji
Gentaro Kumagai
Chikako Miyauchi Hara
Hirotaka James Okano
Atsushi Miyawaki
Yoshiaki Toyama
Hideyuki Okano
Masaya Nakamura
spellingShingle Yuichiro Takahashi
Osahiko Tsuji
Gentaro Kumagai
Chikako Miyauchi Hara
Hirotaka James Okano
Atsushi Miyawaki
Yoshiaki Toyama
Hideyuki Okano
Masaya Nakamura
Comparative Study of Methods for Administering Neural Stem/Progenitor Cells to Treat Spinal Cord Injury in Mice
Cell Transplantation
author_facet Yuichiro Takahashi
Osahiko Tsuji
Gentaro Kumagai
Chikako Miyauchi Hara
Hirotaka James Okano
Atsushi Miyawaki
Yoshiaki Toyama
Hideyuki Okano
Masaya Nakamura
author_sort Yuichiro Takahashi
title Comparative Study of Methods for Administering Neural Stem/Progenitor Cells to Treat Spinal Cord Injury in Mice
title_short Comparative Study of Methods for Administering Neural Stem/Progenitor Cells to Treat Spinal Cord Injury in Mice
title_full Comparative Study of Methods for Administering Neural Stem/Progenitor Cells to Treat Spinal Cord Injury in Mice
title_fullStr Comparative Study of Methods for Administering Neural Stem/Progenitor Cells to Treat Spinal Cord Injury in Mice
title_full_unstemmed Comparative Study of Methods for Administering Neural Stem/Progenitor Cells to Treat Spinal Cord Injury in Mice
title_sort comparative study of methods for administering neural stem/progenitor cells to treat spinal cord injury in mice
publisher SAGE Publishing
series Cell Transplantation
issn 0963-6897
1555-3892
publishDate 2011-06-01
description To investigate potential cures for spinal cord injury (SCI), several researchers have transplanted neural stem/progenitor cells (NS/PCs) into the injured spinal cord by different procedures, including intralesional (IL), intrathecal (IT), and intravenous (IV) injection. However, there are no reports quantifying or comparing the number of cells successfully transplanted to the lesion site by each procedure in vivo. The purpose of the present study was to determine the optimal method of cell transplantation to the SCI site in terms of grafted cell survival and safety. For this purpose, we developed mouse NS/PCs that expressed a novel Venus-luciferase fusion protein that enabled us to detect a minimum of 1,000 grafted cells in vivo by bioluminescence imaging (BLI). After inducing contusive SCI at the T10 level in mice, NS/PCs were transplanted into the injured animals three different ways: by IL, IT, or IV injection. Six weeks after the transplantation, BLI analysis showed that in the IL group, the luminescence intensity of the grafted cells had decreased to about 10% of its initial level, and appeared at the site of injury. In the IT group, the luminescence of the grafted cells, which was distributed throughout the entire subarachnoid space immediately after transplantation, was detected at the injured site 1 week later, and by 6 weeks had gradually decreased to about 0.3% of its initial level. In the IV group, no grafted cells were detected at the site of injury, but all of these mice showed luminescence in the bilateral chest, suggesting pulmonary embolism. In addition, one third of these mice died immediately after the IV injection. In terms of grafted cell survival and safety, we conclude that the IL application of NS/PCs is the most effective and feasible method for transplanting NS/PCs into the SCI site.
url https://doi.org/10.3727/096368910X536554
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