Mature Adipocyte-Derived Cells, Dedifferentiated Fat Cells (DFAT), Promoted Functional Recovery from Spinal Cord Injury-Induced Motor Dysfunction in Rats
Transplantation of mature adipocyte-derived cells (dedifferentiated fat cells) led to marked functional recovery from spinal cord injury (SCI)-induced motor dysfunction in rats. When mature adipocytes were isolated from rat adipose tissue and grown in ceiling culture, transformation into fibroblast-...
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doaj-be7f3261e489401d869fa94efd6acfb82020-11-25T03:32:21ZengSAGE PublishingCell Transplantation0963-68971555-38922008-08-011710.3727/096368908786576516Mature Adipocyte-Derived Cells, Dedifferentiated Fat Cells (DFAT), Promoted Functional Recovery from Spinal Cord Injury-Induced Motor Dysfunction in RatsYuki Ohta0Mitsuko Takenaga1Yukie Tokura2Akemi Hamaguchi3Taro Matsumoto4Koichiro Kano5Hideo Mugishima6Hideyuki Okano7Rie Igarashi8Institute of Medical Science, St. Marianna University School of Medicine, Kawasaki 216-8512, JapanInstitute of Medical Science, St. Marianna University School of Medicine, Kawasaki 216-8512, JapanInstitute of Medical Science, St. Marianna University School of Medicine, Kawasaki 216-8512, JapanInstitute of Medical Science, St. Marianna University School of Medicine, Kawasaki 216-8512, JapanDivision of Cell Regeneration and Transplantation, Advanced Medical Research Center, Nihon University School of Medicine, Tokyo 173-8610, JapanDepartment of Animal Sciences, College of Bioresource Sciences, Nihon University, Fujisawa 252-8510, JapanDivision of Cell Regeneration and Transplantation, Advanced Medical Research Center, Nihon University School of Medicine, Tokyo 173-8610, JapanDepartment of Physiology, Keio University School of Medicine, Tokyo 160-8582, JapanInstitute of Medical Science, St. Marianna University School of Medicine, Kawasaki 216-8512, JapanTransplantation of mature adipocyte-derived cells (dedifferentiated fat cells) led to marked functional recovery from spinal cord injury (SCI)-induced motor dysfunction in rats. When mature adipocytes were isolated from rat adipose tissue and grown in ceiling culture, transformation into fibroblast-like cells without lipid droplets occurred. These fibroblast-like cells, termed dedifferentiated fat cells (DFAT), could proliferate and could also differentiate back into adipocytes. DFAT expressed neural markers such as nestin, βIII tubulin, and GFAP. Allografting of DFAT into SCI-induced rats led to significant recovery from hindlimb dysfunction. Grafted cells were detected at the injection site, and some of these cells expressed βIII tubulin. DFAT expressed neurotrophic factors such as BDNF and GDNF prior to transplantation, and grafted cells were also positive for these factors. Therefore, these neurotrophic factors derived from grafted DFAT might have contributed to the promotion of functional recovery. These findings also suggest that mature adipocytes could become a new source for cell replacement therapy to treat central nervous system disorders.https://doi.org/10.3727/096368908786576516 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Yuki Ohta Mitsuko Takenaga Yukie Tokura Akemi Hamaguchi Taro Matsumoto Koichiro Kano Hideo Mugishima Hideyuki Okano Rie Igarashi |
spellingShingle |
Yuki Ohta Mitsuko Takenaga Yukie Tokura Akemi Hamaguchi Taro Matsumoto Koichiro Kano Hideo Mugishima Hideyuki Okano Rie Igarashi Mature Adipocyte-Derived Cells, Dedifferentiated Fat Cells (DFAT), Promoted Functional Recovery from Spinal Cord Injury-Induced Motor Dysfunction in Rats Cell Transplantation |
author_facet |
Yuki Ohta Mitsuko Takenaga Yukie Tokura Akemi Hamaguchi Taro Matsumoto Koichiro Kano Hideo Mugishima Hideyuki Okano Rie Igarashi |
author_sort |
Yuki Ohta |
title |
Mature Adipocyte-Derived Cells, Dedifferentiated Fat Cells (DFAT), Promoted Functional Recovery from Spinal Cord Injury-Induced Motor Dysfunction in Rats |
title_short |
Mature Adipocyte-Derived Cells, Dedifferentiated Fat Cells (DFAT), Promoted Functional Recovery from Spinal Cord Injury-Induced Motor Dysfunction in Rats |
title_full |
Mature Adipocyte-Derived Cells, Dedifferentiated Fat Cells (DFAT), Promoted Functional Recovery from Spinal Cord Injury-Induced Motor Dysfunction in Rats |
title_fullStr |
Mature Adipocyte-Derived Cells, Dedifferentiated Fat Cells (DFAT), Promoted Functional Recovery from Spinal Cord Injury-Induced Motor Dysfunction in Rats |
title_full_unstemmed |
Mature Adipocyte-Derived Cells, Dedifferentiated Fat Cells (DFAT), Promoted Functional Recovery from Spinal Cord Injury-Induced Motor Dysfunction in Rats |
title_sort |
mature adipocyte-derived cells, dedifferentiated fat cells (dfat), promoted functional recovery from spinal cord injury-induced motor dysfunction in rats |
publisher |
SAGE Publishing |
series |
Cell Transplantation |
issn |
0963-6897 1555-3892 |
publishDate |
2008-08-01 |
description |
Transplantation of mature adipocyte-derived cells (dedifferentiated fat cells) led to marked functional recovery from spinal cord injury (SCI)-induced motor dysfunction in rats. When mature adipocytes were isolated from rat adipose tissue and grown in ceiling culture, transformation into fibroblast-like cells without lipid droplets occurred. These fibroblast-like cells, termed dedifferentiated fat cells (DFAT), could proliferate and could also differentiate back into adipocytes. DFAT expressed neural markers such as nestin, βIII tubulin, and GFAP. Allografting of DFAT into SCI-induced rats led to significant recovery from hindlimb dysfunction. Grafted cells were detected at the injection site, and some of these cells expressed βIII tubulin. DFAT expressed neurotrophic factors such as BDNF and GDNF prior to transplantation, and grafted cells were also positive for these factors. Therefore, these neurotrophic factors derived from grafted DFAT might have contributed to the promotion of functional recovery. These findings also suggest that mature adipocytes could become a new source for cell replacement therapy to treat central nervous system disorders. |
url |
https://doi.org/10.3727/096368908786576516 |
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