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Autologous adipose-derived stem cell transplantation enhances healing of wound with exposed bone in a rat model

OBJECTIVES: Soft tissue wounds with exposed bone often require extended healing times and can be associated with severe complications. We describe the ability of artificial dermis with autogenic adipose-derived stem cells (ADSCs) to promote the healing of wounds with exposed bone in a rat model. MET...

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Autores principales: Hamada, Tomo, Matsubara, Hidenori, Yoshida, Yasuhisa, Ugaji, Shuhei, Nomura, Issei, Tsuchiya, Hiroyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6513073/
https://www.ncbi.nlm.nih.gov/pubmed/31083652
http://dx.doi.org/10.1371/journal.pone.0214106
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author Hamada, Tomo
Matsubara, Hidenori
Yoshida, Yasuhisa
Ugaji, Shuhei
Nomura, Issei
Tsuchiya, Hiroyuki
author_facet Hamada, Tomo
Matsubara, Hidenori
Yoshida, Yasuhisa
Ugaji, Shuhei
Nomura, Issei
Tsuchiya, Hiroyuki
author_sort Hamada, Tomo
collection PubMed
description OBJECTIVES: Soft tissue wounds with exposed bone often require extended healing times and can be associated with severe complications. We describe the ability of artificial dermis with autogenic adipose-derived stem cells (ADSCs) to promote the healing of wounds with exposed bone in a rat model. METHODS: Adipose tissues harvested from the bilateral inguinal regions of Wistar rats were used as ADSCs. Rats were randomly divided into control and ADSC groups to investigate the efficacy of ADSC transplantation for wound healing (n = 20 per group). Soft tissue defects were created on the heads of the rats and were covered with artificial dermis with or without the seeded ADSCs. Specimens from these rats were evaluated using digital image analysis, histology, immunohistochemistry, cell labeling, and real-time reverse-transcription polymerase chain reaction (real-time RT-PCR). RESULTS: The average global wound area was significantly smaller in the ADSC group than in the control group on days 3, 7, and 14 after surgery (p<0.05). After 14 days, the blood vessel density in the wound increased by 1.6-fold in the ADSC group compared with that in the control group (p<0.01). Real-time RT-PCR results showed higher Fgfb and Vegf expression levels at all time points, and higher Tgfb1 and Tgfb3 expression levels until 14 days after surgery in the ADSC group than in the control group (p<0.05). CONCLUSIONS: In wounds with exposed bone, autogenic ADSCs can promote vascularization and wound healing. Use of this cell source has multiple benefits, including convenient clinical application and lack of ethical concerns.
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spelling pubmed-65130732019-05-31 Autologous adipose-derived stem cell transplantation enhances healing of wound with exposed bone in a rat model Hamada, Tomo Matsubara, Hidenori Yoshida, Yasuhisa Ugaji, Shuhei Nomura, Issei Tsuchiya, Hiroyuki PLoS One Research Article OBJECTIVES: Soft tissue wounds with exposed bone often require extended healing times and can be associated with severe complications. We describe the ability of artificial dermis with autogenic adipose-derived stem cells (ADSCs) to promote the healing of wounds with exposed bone in a rat model. METHODS: Adipose tissues harvested from the bilateral inguinal regions of Wistar rats were used as ADSCs. Rats were randomly divided into control and ADSC groups to investigate the efficacy of ADSC transplantation for wound healing (n = 20 per group). Soft tissue defects were created on the heads of the rats and were covered with artificial dermis with or without the seeded ADSCs. Specimens from these rats were evaluated using digital image analysis, histology, immunohistochemistry, cell labeling, and real-time reverse-transcription polymerase chain reaction (real-time RT-PCR). RESULTS: The average global wound area was significantly smaller in the ADSC group than in the control group on days 3, 7, and 14 after surgery (p<0.05). After 14 days, the blood vessel density in the wound increased by 1.6-fold in the ADSC group compared with that in the control group (p<0.01). Real-time RT-PCR results showed higher Fgfb and Vegf expression levels at all time points, and higher Tgfb1 and Tgfb3 expression levels until 14 days after surgery in the ADSC group than in the control group (p<0.05). CONCLUSIONS: In wounds with exposed bone, autogenic ADSCs can promote vascularization and wound healing. Use of this cell source has multiple benefits, including convenient clinical application and lack of ethical concerns. Public Library of Science 2019-05-13 /pmc/articles/PMC6513073/ /pubmed/31083652 http://dx.doi.org/10.1371/journal.pone.0214106 Text en © 2019 Hamada 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Hamada, Tomo
Matsubara, Hidenori
Yoshida, Yasuhisa
Ugaji, Shuhei
Nomura, Issei
Tsuchiya, Hiroyuki
Autologous adipose-derived stem cell transplantation enhances healing of wound with exposed bone in a rat model
title Autologous adipose-derived stem cell transplantation enhances healing of wound with exposed bone in a rat model
title_full Autologous adipose-derived stem cell transplantation enhances healing of wound with exposed bone in a rat model
title_fullStr Autologous adipose-derived stem cell transplantation enhances healing of wound with exposed bone in a rat model
title_full_unstemmed Autologous adipose-derived stem cell transplantation enhances healing of wound with exposed bone in a rat model
title_short Autologous adipose-derived stem cell transplantation enhances healing of wound with exposed bone in a rat model
title_sort autologous adipose-derived stem cell transplantation enhances healing of wound with exposed bone in a rat model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6513073/
https://www.ncbi.nlm.nih.gov/pubmed/31083652
http://dx.doi.org/10.1371/journal.pone.0214106
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