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Pharmacological Mobilization and Recruitment of Stem Cells in Rats Stops Abdominal Adhesions After Laparotomy

Adhesions are a very common complication in the abdominal surgery. Animal studies and human trials have evaluated strategies designed to reduce and prevent postsurgical adhesions but few have an evidence base that justifies routine use. A strategy to prevent adhesions effectively remains an urgent n...

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Autores principales: Iwasaki, Kenichi, Ahmadi, Ali Reza, Qi, Le, Chen, Melissa, Wang, Wei, Katsumata, Kenji, Tsuchida, Akihiko, Burdick, James, Cameron, Andrew M., Sun, Zhaoli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6509124/
https://www.ncbi.nlm.nih.gov/pubmed/31073167
http://dx.doi.org/10.1038/s41598-019-43734-1
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author Iwasaki, Kenichi
Ahmadi, Ali Reza
Qi, Le
Chen, Melissa
Wang, Wei
Katsumata, Kenji
Tsuchida, Akihiko
Burdick, James
Cameron, Andrew M.
Sun, Zhaoli
author_facet Iwasaki, Kenichi
Ahmadi, Ali Reza
Qi, Le
Chen, Melissa
Wang, Wei
Katsumata, Kenji
Tsuchida, Akihiko
Burdick, James
Cameron, Andrew M.
Sun, Zhaoli
author_sort Iwasaki, Kenichi
collection PubMed
description Adhesions are a very common complication in the abdominal surgery. Animal studies and human trials have evaluated strategies designed to reduce and prevent postsurgical adhesions but few have an evidence base that justifies routine use. A strategy to prevent adhesions effectively remains an urgent need. We studied a reproducible model of intra-peritoneal adhesion formation in rats using laparotomy with several peritoneal sutures to produce the adhesions. Here we show that entraining endogenous stem cells into injury sites using the combined effect of AMD3100 and low-dose FK-506 (AF) can reduce the adhesion score significantly and abolish peritoneal adhesions in 45% of animals in a rat model of severe postsurgical intra-abdominal adhesions, compared with saline controls. Searching for mechanisms, we found AF treatment dramatically increased SDF-1 expressing cells, HGF expressing Ym1+ M2 macrophages and CD133+ stem cells in the injury sites of peritoneal surface at day 5 post-operation. Our results demonstrate that medically induced recruitment of autologous stem cells using AF significantly reduced postsurgical intra-abdominal adhesions. These findings suggest a novel effective therapeutic approach to preventing adhesions in patients.
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spelling pubmed-65091242019-05-22 Pharmacological Mobilization and Recruitment of Stem Cells in Rats Stops Abdominal Adhesions After Laparotomy Iwasaki, Kenichi Ahmadi, Ali Reza Qi, Le Chen, Melissa Wang, Wei Katsumata, Kenji Tsuchida, Akihiko Burdick, James Cameron, Andrew M. Sun, Zhaoli Sci Rep Article Adhesions are a very common complication in the abdominal surgery. Animal studies and human trials have evaluated strategies designed to reduce and prevent postsurgical adhesions but few have an evidence base that justifies routine use. A strategy to prevent adhesions effectively remains an urgent need. We studied a reproducible model of intra-peritoneal adhesion formation in rats using laparotomy with several peritoneal sutures to produce the adhesions. Here we show that entraining endogenous stem cells into injury sites using the combined effect of AMD3100 and low-dose FK-506 (AF) can reduce the adhesion score significantly and abolish peritoneal adhesions in 45% of animals in a rat model of severe postsurgical intra-abdominal adhesions, compared with saline controls. Searching for mechanisms, we found AF treatment dramatically increased SDF-1 expressing cells, HGF expressing Ym1+ M2 macrophages and CD133+ stem cells in the injury sites of peritoneal surface at day 5 post-operation. Our results demonstrate that medically induced recruitment of autologous stem cells using AF significantly reduced postsurgical intra-abdominal adhesions. These findings suggest a novel effective therapeutic approach to preventing adhesions in patients. Nature Publishing Group UK 2019-05-09 /pmc/articles/PMC6509124/ /pubmed/31073167 http://dx.doi.org/10.1038/s41598-019-43734-1 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Iwasaki, Kenichi
Ahmadi, Ali Reza
Qi, Le
Chen, Melissa
Wang, Wei
Katsumata, Kenji
Tsuchida, Akihiko
Burdick, James
Cameron, Andrew M.
Sun, Zhaoli
Pharmacological Mobilization and Recruitment of Stem Cells in Rats Stops Abdominal Adhesions After Laparotomy
title Pharmacological Mobilization and Recruitment of Stem Cells in Rats Stops Abdominal Adhesions After Laparotomy
title_full Pharmacological Mobilization and Recruitment of Stem Cells in Rats Stops Abdominal Adhesions After Laparotomy
title_fullStr Pharmacological Mobilization and Recruitment of Stem Cells in Rats Stops Abdominal Adhesions After Laparotomy
title_full_unstemmed Pharmacological Mobilization and Recruitment of Stem Cells in Rats Stops Abdominal Adhesions After Laparotomy
title_short Pharmacological Mobilization and Recruitment of Stem Cells in Rats Stops Abdominal Adhesions After Laparotomy
title_sort pharmacological mobilization and recruitment of stem cells in rats stops abdominal adhesions after laparotomy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6509124/
https://www.ncbi.nlm.nih.gov/pubmed/31073167
http://dx.doi.org/10.1038/s41598-019-43734-1
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