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Efficient cell transplantation combining injectable hydrogels with control release of growth factors

INTRODUCTION: The objective of this study is to investigate the effect of gelatin microspheres incorporating growth factors on the therapeutic efficacy in cell transplantation. The strength of this study is to combine gelatin hydrogel microspheres incorporating basic fibroblast growth factor and pla...

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Autores principales: Mitsui, Ryo, Matsukawa, Makoto, Nakagawa, Kiyoko, Isomura, Emiko, Kuwahara, Toshie, Nii, Teruki, Tanaka, Susumu, Tabata, Yasuhiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Japanese Society for Regenerative Medicine 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8479297/
https://www.ncbi.nlm.nih.gov/pubmed/34632010
http://dx.doi.org/10.1016/j.reth.2021.09.003
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author Mitsui, Ryo
Matsukawa, Makoto
Nakagawa, Kiyoko
Isomura, Emiko
Kuwahara, Toshie
Nii, Teruki
Tanaka, Susumu
Tabata, Yasuhiko
author_facet Mitsui, Ryo
Matsukawa, Makoto
Nakagawa, Kiyoko
Isomura, Emiko
Kuwahara, Toshie
Nii, Teruki
Tanaka, Susumu
Tabata, Yasuhiko
author_sort Mitsui, Ryo
collection PubMed
description INTRODUCTION: The objective of this study is to investigate the effect of gelatin microspheres incorporating growth factors on the therapeutic efficacy in cell transplantation. The strength of this study is to combine gelatin hydrogel microspheres incorporating basic fibroblast growth factor and platelet growth factor mixture (GM/GF) with bioabsorbable injectable hydrogels (iGel) for transplantation of adipose-derived stem cells (ASCs). METHODS: The rats ASCs suspended in various solutions were transplanted in masseter muscle. Rats were euthanized 2, 7, 14 days after injection for measurement of the number of ASCs retention in the muscle and morphological evaluation of muscle fibers and the inflammation of the injected tissue by histologic and immunofluorescent stain. RESULTS: Following the injection into the skeletal muscle, the GM/GF allowed the growth factors to release at the injection site over one week. When ASCs were transplanted into skeletal muscle using iGel incorporating GM/GF (iGel+GM/GF), the number of cells grafted was significantly high compared with other control groups. Moreover, for the groups to which GM/GF was added, the cells transplanted survived, and the Myo-D expression of a myoblast marker was observed at the region of cells transplanted. CONCLUSIONS: The growth factors released for a long time likely enhance the proliferative and differentiative capacity of cells. The simple combination with iGel and GM/GF allowed ASCs to enhance their survival at the injected site and consequently achieve improved therapeutic efficacy in cell transplantation.
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spelling pubmed-84792972021-10-07 Efficient cell transplantation combining injectable hydrogels with control release of growth factors Mitsui, Ryo Matsukawa, Makoto Nakagawa, Kiyoko Isomura, Emiko Kuwahara, Toshie Nii, Teruki Tanaka, Susumu Tabata, Yasuhiko Regen Ther Original Article INTRODUCTION: The objective of this study is to investigate the effect of gelatin microspheres incorporating growth factors on the therapeutic efficacy in cell transplantation. The strength of this study is to combine gelatin hydrogel microspheres incorporating basic fibroblast growth factor and platelet growth factor mixture (GM/GF) with bioabsorbable injectable hydrogels (iGel) for transplantation of adipose-derived stem cells (ASCs). METHODS: The rats ASCs suspended in various solutions were transplanted in masseter muscle. Rats were euthanized 2, 7, 14 days after injection for measurement of the number of ASCs retention in the muscle and morphological evaluation of muscle fibers and the inflammation of the injected tissue by histologic and immunofluorescent stain. RESULTS: Following the injection into the skeletal muscle, the GM/GF allowed the growth factors to release at the injection site over one week. When ASCs were transplanted into skeletal muscle using iGel incorporating GM/GF (iGel+GM/GF), the number of cells grafted was significantly high compared with other control groups. Moreover, for the groups to which GM/GF was added, the cells transplanted survived, and the Myo-D expression of a myoblast marker was observed at the region of cells transplanted. CONCLUSIONS: The growth factors released for a long time likely enhance the proliferative and differentiative capacity of cells. The simple combination with iGel and GM/GF allowed ASCs to enhance their survival at the injected site and consequently achieve improved therapeutic efficacy in cell transplantation. Japanese Society for Regenerative Medicine 2021-09-25 /pmc/articles/PMC8479297/ /pubmed/34632010 http://dx.doi.org/10.1016/j.reth.2021.09.003 Text en © 2021 The Japanese Society for Regenerative Medicine. Production and hosting by Elsevier B.V. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Mitsui, Ryo
Matsukawa, Makoto
Nakagawa, Kiyoko
Isomura, Emiko
Kuwahara, Toshie
Nii, Teruki
Tanaka, Susumu
Tabata, Yasuhiko
Efficient cell transplantation combining injectable hydrogels with control release of growth factors
title Efficient cell transplantation combining injectable hydrogels with control release of growth factors
title_full Efficient cell transplantation combining injectable hydrogels with control release of growth factors
title_fullStr Efficient cell transplantation combining injectable hydrogels with control release of growth factors
title_full_unstemmed Efficient cell transplantation combining injectable hydrogels with control release of growth factors
title_short Efficient cell transplantation combining injectable hydrogels with control release of growth factors
title_sort efficient cell transplantation combining injectable hydrogels with control release of growth factors
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8479297/
https://www.ncbi.nlm.nih.gov/pubmed/34632010
http://dx.doi.org/10.1016/j.reth.2021.09.003
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