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Local Delivery of Mesenchymal Stem Cells with Poly-Lactic-Co-Glycolic Acid Nano-Fiber Scaffold Suppress Arthritis in Rats
Mesenchymal stem cells (MSC) have been used recently for the treatment of autoimmune diseases in murine animal models due to the immunoregulatory capacity. Current utilization of MSC requires cells in certain quantity with multiple courses of administration, leading to limitation in clinical usage....
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4256456/ https://www.ncbi.nlm.nih.gov/pubmed/25474102 http://dx.doi.org/10.1371/journal.pone.0114621 |
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author | Zhang, Xiangmei Yamaoka, Kunihiro Sonomoto, Koshiro Kaneko, Hiroaki Satake, Makoto Yamamoto, Yuka Kondo, Masahiro Zhao, Jidong Miyagawa, Ippei Yamagata, Kaoru Fukuyo, Shunsuke Okada, Yosuke Tanaka, Yoshiya |
author_facet | Zhang, Xiangmei Yamaoka, Kunihiro Sonomoto, Koshiro Kaneko, Hiroaki Satake, Makoto Yamamoto, Yuka Kondo, Masahiro Zhao, Jidong Miyagawa, Ippei Yamagata, Kaoru Fukuyo, Shunsuke Okada, Yosuke Tanaka, Yoshiya |
author_sort | Zhang, Xiangmei |
collection | PubMed |
description | Mesenchymal stem cells (MSC) have been used recently for the treatment of autoimmune diseases in murine animal models due to the immunoregulatory capacity. Current utilization of MSC requires cells in certain quantity with multiple courses of administration, leading to limitation in clinical usage. Here we efficiently treated collagen-induced arthritis rats with a single local implantation with reduced number of MSC (2∼20% of previous studies) with nano-fiber poly-lactic-co-glycolic acid (nano-fiber) scaffold. MSC seeded on nano-fiber scaffold suppressed arthritis and bone destruction due to inhibition of systemic inflammatory reaction and immune response by suppressing T cell proliferation and reducing anti- type II collagen antibody production. In vivo tracing of MSC demonstrated that these cells remained within the scaffold without migrating to other organs. Meanwhile, in vitro culture of MSC with nano-fiber scaffold significantly increased TGF-β1 production. These results indicate an efficient utilization of MSC with the scaffold for destructive joints in rheumatoid arthritis by a single and local inoculation. Thus, our data may serve as a new strategy for MSC-based therapy in inflammatory diseases and an alternative delivery method for bone destruction treatment. |
format | Online Article Text |
id | pubmed-4256456 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-42564562014-12-11 Local Delivery of Mesenchymal Stem Cells with Poly-Lactic-Co-Glycolic Acid Nano-Fiber Scaffold Suppress Arthritis in Rats Zhang, Xiangmei Yamaoka, Kunihiro Sonomoto, Koshiro Kaneko, Hiroaki Satake, Makoto Yamamoto, Yuka Kondo, Masahiro Zhao, Jidong Miyagawa, Ippei Yamagata, Kaoru Fukuyo, Shunsuke Okada, Yosuke Tanaka, Yoshiya PLoS One Research Article Mesenchymal stem cells (MSC) have been used recently for the treatment of autoimmune diseases in murine animal models due to the immunoregulatory capacity. Current utilization of MSC requires cells in certain quantity with multiple courses of administration, leading to limitation in clinical usage. Here we efficiently treated collagen-induced arthritis rats with a single local implantation with reduced number of MSC (2∼20% of previous studies) with nano-fiber poly-lactic-co-glycolic acid (nano-fiber) scaffold. MSC seeded on nano-fiber scaffold suppressed arthritis and bone destruction due to inhibition of systemic inflammatory reaction and immune response by suppressing T cell proliferation and reducing anti- type II collagen antibody production. In vivo tracing of MSC demonstrated that these cells remained within the scaffold without migrating to other organs. Meanwhile, in vitro culture of MSC with nano-fiber scaffold significantly increased TGF-β1 production. These results indicate an efficient utilization of MSC with the scaffold for destructive joints in rheumatoid arthritis by a single and local inoculation. Thus, our data may serve as a new strategy for MSC-based therapy in inflammatory diseases and an alternative delivery method for bone destruction treatment. Public Library of Science 2014-12-04 /pmc/articles/PMC4256456/ /pubmed/25474102 http://dx.doi.org/10.1371/journal.pone.0114621 Text en © 2014 Zhang 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Zhang, Xiangmei Yamaoka, Kunihiro Sonomoto, Koshiro Kaneko, Hiroaki Satake, Makoto Yamamoto, Yuka Kondo, Masahiro Zhao, Jidong Miyagawa, Ippei Yamagata, Kaoru Fukuyo, Shunsuke Okada, Yosuke Tanaka, Yoshiya Local Delivery of Mesenchymal Stem Cells with Poly-Lactic-Co-Glycolic Acid Nano-Fiber Scaffold Suppress Arthritis in Rats |
title | Local Delivery of Mesenchymal Stem Cells with Poly-Lactic-Co-Glycolic Acid Nano-Fiber Scaffold Suppress Arthritis in Rats |
title_full | Local Delivery of Mesenchymal Stem Cells with Poly-Lactic-Co-Glycolic Acid Nano-Fiber Scaffold Suppress Arthritis in Rats |
title_fullStr | Local Delivery of Mesenchymal Stem Cells with Poly-Lactic-Co-Glycolic Acid Nano-Fiber Scaffold Suppress Arthritis in Rats |
title_full_unstemmed | Local Delivery of Mesenchymal Stem Cells with Poly-Lactic-Co-Glycolic Acid Nano-Fiber Scaffold Suppress Arthritis in Rats |
title_short | Local Delivery of Mesenchymal Stem Cells with Poly-Lactic-Co-Glycolic Acid Nano-Fiber Scaffold Suppress Arthritis in Rats |
title_sort | local delivery of mesenchymal stem cells with poly-lactic-co-glycolic acid nano-fiber scaffold suppress arthritis in rats |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4256456/ https://www.ncbi.nlm.nih.gov/pubmed/25474102 http://dx.doi.org/10.1371/journal.pone.0114621 |
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