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Bone marrow-derived mesenchymal stem cells migrate to healthy and damaged salivary glands following stem cell infusion

Xerostomia is a severe side effect of radiation therapy in head and neck cancer patients. To date, no satisfactory treatment option has been established. Because mesenchymal stem cells (MSCs) have been identified as a potential treatment modality, we aimed to evaluate stem cell distribution followin...

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Autores principales: Schwarz, Silke, Huss, Ralf, Schulz-Siegmund, Michaela, Vogel, Breda, Brandau, Sven, Lang, Stephan, Rotter, Nicole
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4170149/
https://www.ncbi.nlm.nih.gov/pubmed/24810808
http://dx.doi.org/10.1038/ijos.2014.23
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author Schwarz, Silke
Huss, Ralf
Schulz-Siegmund, Michaela
Vogel, Breda
Brandau, Sven
Lang, Stephan
Rotter, Nicole
author_facet Schwarz, Silke
Huss, Ralf
Schulz-Siegmund, Michaela
Vogel, Breda
Brandau, Sven
Lang, Stephan
Rotter, Nicole
author_sort Schwarz, Silke
collection PubMed
description Xerostomia is a severe side effect of radiation therapy in head and neck cancer patients. To date, no satisfactory treatment option has been established. Because mesenchymal stem cells (MSCs) have been identified as a potential treatment modality, we aimed to evaluate stem cell distribution following intravenous and intraglandular injections using a surgical model of salivary gland damage and to analyse the effects of MSC injections on the recruitment of immune cells. The submandibular gland ducts of rats were surgically ligated. Syngeneic adult MSCs were isolated, immortalised by simian virus 40 (SV40) large T antigen and characterized by flow cytometry. MSCs were injected intravenously and intraglandularly. After 1, 3 and 7 days, the organs of interest were analysed for stem cell recruitment. Inflammation was analysed by immunohistochemical staining. We were able to demonstrate that, after intravenous injection, MSCs were recruited to normal and damaged submandibular glands on days 1, 3 and 7. Unexpectedly, stem cells were recruited to ligated and non-ligated glands in a comparable manner. After intraglandular injection of MSCs into ligated glands, the presence of MSCs, leucocytes and macrophages was enhanced, compared to intravenous injection of stem cells. Our data suggest that injected MSCs were retained within the inflamed glands, could become activated and subsequently recruited leucocytes to the sites of tissue damage.
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spelling pubmed-41701492014-09-24 Bone marrow-derived mesenchymal stem cells migrate to healthy and damaged salivary glands following stem cell infusion Schwarz, Silke Huss, Ralf Schulz-Siegmund, Michaela Vogel, Breda Brandau, Sven Lang, Stephan Rotter, Nicole Int J Oral Sci Original Article Xerostomia is a severe side effect of radiation therapy in head and neck cancer patients. To date, no satisfactory treatment option has been established. Because mesenchymal stem cells (MSCs) have been identified as a potential treatment modality, we aimed to evaluate stem cell distribution following intravenous and intraglandular injections using a surgical model of salivary gland damage and to analyse the effects of MSC injections on the recruitment of immune cells. The submandibular gland ducts of rats were surgically ligated. Syngeneic adult MSCs were isolated, immortalised by simian virus 40 (SV40) large T antigen and characterized by flow cytometry. MSCs were injected intravenously and intraglandularly. After 1, 3 and 7 days, the organs of interest were analysed for stem cell recruitment. Inflammation was analysed by immunohistochemical staining. We were able to demonstrate that, after intravenous injection, MSCs were recruited to normal and damaged submandibular glands on days 1, 3 and 7. Unexpectedly, stem cells were recruited to ligated and non-ligated glands in a comparable manner. After intraglandular injection of MSCs into ligated glands, the presence of MSCs, leucocytes and macrophages was enhanced, compared to intravenous injection of stem cells. Our data suggest that injected MSCs were retained within the inflamed glands, could become activated and subsequently recruited leucocytes to the sites of tissue damage. Nature Publishing Group 2014-09 2014-05-09 /pmc/articles/PMC4170149/ /pubmed/24810808 http://dx.doi.org/10.1038/ijos.2014.23 Text en Copyright © 2014 West China School of Stomatology http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/
spellingShingle Original Article
Schwarz, Silke
Huss, Ralf
Schulz-Siegmund, Michaela
Vogel, Breda
Brandau, Sven
Lang, Stephan
Rotter, Nicole
Bone marrow-derived mesenchymal stem cells migrate to healthy and damaged salivary glands following stem cell infusion
title Bone marrow-derived mesenchymal stem cells migrate to healthy and damaged salivary glands following stem cell infusion
title_full Bone marrow-derived mesenchymal stem cells migrate to healthy and damaged salivary glands following stem cell infusion
title_fullStr Bone marrow-derived mesenchymal stem cells migrate to healthy and damaged salivary glands following stem cell infusion
title_full_unstemmed Bone marrow-derived mesenchymal stem cells migrate to healthy and damaged salivary glands following stem cell infusion
title_short Bone marrow-derived mesenchymal stem cells migrate to healthy and damaged salivary glands following stem cell infusion
title_sort bone marrow-derived mesenchymal stem cells migrate to healthy and damaged salivary glands following stem cell infusion
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4170149/
https://www.ncbi.nlm.nih.gov/pubmed/24810808
http://dx.doi.org/10.1038/ijos.2014.23
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