No Immunogenicity of IPS Cells in Syngeneic Host Studied by In Vivo Injection and 3D Scaffold Experiments
Induced Pluripotent Stem Cells (IPSCs) open the great possibility to employ patient’s own tissue to the previously incurable diseases. However these cells can be used in cell therapy only if they are not rejected when transplanted back into the syngeneic host. We found that the injection of iPSCs de...
Main Authors: | , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Hindawi Limited
2013-01-01
|
Series: | BioMed Research International |
Online Access: | http://dx.doi.org/10.1155/2013/378207 |
id |
doaj-8d1c963f0c0c4d00944aa9e6deccd177 |
---|---|
record_format |
Article |
spelling |
doaj-8d1c963f0c0c4d00944aa9e6deccd1772020-11-24T23:07:18ZengHindawi LimitedBioMed Research International2314-61332314-61412013-01-01201310.1155/2013/378207378207No Immunogenicity of IPS Cells in Syngeneic Host Studied by In Vivo Injection and 3D Scaffold ExperimentsSuganya Thanasegaran0Zhao Cheng1Sachiko Ito2Naomi Nishio3Ken-ichi Isobe4Department of Immunology, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya 466-8550, JapanDepartment of Immunology, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya 466-8550, JapanDepartment of Immunology, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya 466-8550, JapanDepartment of Immunology, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya 466-8550, JapanDepartment of Immunology, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya 466-8550, JapanInduced Pluripotent Stem Cells (IPSCs) open the great possibility to employ patient’s own tissue to the previously incurable diseases. However these cells can be used in cell therapy only if they are not rejected when transplanted back into the syngeneic host. We found that the injection of iPSCs derived from different ages of mice into syngeneic C57BL/6 mice produced teratoma and was not rejected. Then we cultured iPSCs and myeloid differentiated iPSCs in three-dimensional porous scaffold and transplanted to C57BL/6 mice and BALB/C mice. After transplantation, we could observe the cell density inside the scaffold increased rapidly in syngeneic mice compared to the allogeneic mice indicating the favorable conditions supporting the growth of iPSCs in vivo. Unlike the allogeneic counterpart, we could not observe few infiltrating T cells inside the scaffold of syngeneic mice. These results contribute to the optimistic view of iPSCs for regenerative medicine in near future.http://dx.doi.org/10.1155/2013/378207 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Suganya Thanasegaran Zhao Cheng Sachiko Ito Naomi Nishio Ken-ichi Isobe |
spellingShingle |
Suganya Thanasegaran Zhao Cheng Sachiko Ito Naomi Nishio Ken-ichi Isobe No Immunogenicity of IPS Cells in Syngeneic Host Studied by In Vivo Injection and 3D Scaffold Experiments BioMed Research International |
author_facet |
Suganya Thanasegaran Zhao Cheng Sachiko Ito Naomi Nishio Ken-ichi Isobe |
author_sort |
Suganya Thanasegaran |
title |
No Immunogenicity of IPS Cells in Syngeneic Host Studied by In Vivo Injection and 3D Scaffold Experiments |
title_short |
No Immunogenicity of IPS Cells in Syngeneic Host Studied by In Vivo Injection and 3D Scaffold Experiments |
title_full |
No Immunogenicity of IPS Cells in Syngeneic Host Studied by In Vivo Injection and 3D Scaffold Experiments |
title_fullStr |
No Immunogenicity of IPS Cells in Syngeneic Host Studied by In Vivo Injection and 3D Scaffold Experiments |
title_full_unstemmed |
No Immunogenicity of IPS Cells in Syngeneic Host Studied by In Vivo Injection and 3D Scaffold Experiments |
title_sort |
no immunogenicity of ips cells in syngeneic host studied by in vivo injection and 3d scaffold experiments |
publisher |
Hindawi Limited |
series |
BioMed Research International |
issn |
2314-6133 2314-6141 |
publishDate |
2013-01-01 |
description |
Induced Pluripotent Stem Cells (IPSCs) open the great possibility to employ patient’s own tissue to the previously incurable diseases. However these cells can be used in cell therapy only if they are not rejected when transplanted back into the syngeneic host. We found that the injection of iPSCs derived from different ages of mice into syngeneic C57BL/6 mice produced teratoma and was not rejected. Then we cultured iPSCs and myeloid differentiated iPSCs in three-dimensional porous scaffold and transplanted to C57BL/6 mice and BALB/C mice. After transplantation, we could observe the cell density inside the scaffold increased rapidly in syngeneic mice compared to the allogeneic mice indicating the favorable conditions supporting the growth of iPSCs in vivo. Unlike the allogeneic counterpart, we could not observe few infiltrating T cells inside the scaffold of syngeneic mice. These results contribute to the optimistic view of iPSCs for regenerative medicine in near future. |
url |
http://dx.doi.org/10.1155/2013/378207 |
work_keys_str_mv |
AT suganyathanasegaran noimmunogenicityofipscellsinsyngeneichoststudiedbyinvivoinjectionand3dscaffoldexperiments AT zhaocheng noimmunogenicityofipscellsinsyngeneichoststudiedbyinvivoinjectionand3dscaffoldexperiments AT sachikoito noimmunogenicityofipscellsinsyngeneichoststudiedbyinvivoinjectionand3dscaffoldexperiments AT naominishio noimmunogenicityofipscellsinsyngeneichoststudiedbyinvivoinjectionand3dscaffoldexperiments AT kenichiisobe noimmunogenicityofipscellsinsyngeneichoststudiedbyinvivoinjectionand3dscaffoldexperiments |
_version_ |
1725618909472620544 |