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The Efficacy of Mesenchymal Stem Cell Transplantation in Caustic Esophagus Injury: An Experimental Study

Introduction. Ingestion of corrosive substances may lead to stricture formation in esophagus as a late complication. Full thickness injury seems to exterminate tissue stem cells of esophagus. Mesenchymal stem cells (MSCs) can differentiate into specific cell lineages and have the capacity of homing...

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Autores principales: Kantarcioglu, Murat, Caliskan, Bahadir, Demirci, Hakan, Karacalioglu, Ozgur, Kekilli, Murat, Polat, Zulfikar, Gunal, Armagan, Akinci, Melih, Uysal, Cagri, Eksert, Sami, Gurel, Hasan, Celebi, Gurkan, Avcu, Ferit, Ural, Ali Ugur, Bagci, Sait
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4027018/
https://www.ncbi.nlm.nih.gov/pubmed/24876849
http://dx.doi.org/10.1155/2014/939674
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author Kantarcioglu, Murat
Caliskan, Bahadir
Demirci, Hakan
Karacalioglu, Ozgur
Kekilli, Murat
Polat, Zulfikar
Gunal, Armagan
Akinci, Melih
Uysal, Cagri
Eksert, Sami
Gurel, Hasan
Celebi, Gurkan
Avcu, Ferit
Ural, Ali Ugur
Bagci, Sait
author_facet Kantarcioglu, Murat
Caliskan, Bahadir
Demirci, Hakan
Karacalioglu, Ozgur
Kekilli, Murat
Polat, Zulfikar
Gunal, Armagan
Akinci, Melih
Uysal, Cagri
Eksert, Sami
Gurel, Hasan
Celebi, Gurkan
Avcu, Ferit
Ural, Ali Ugur
Bagci, Sait
author_sort Kantarcioglu, Murat
collection PubMed
description Introduction. Ingestion of corrosive substances may lead to stricture formation in esophagus as a late complication. Full thickness injury seems to exterminate tissue stem cells of esophagus. Mesenchymal stem cells (MSCs) can differentiate into specific cell lineages and have the capacity of homing in sites of injury. Aim and Methods. We aimed to investigate the efficacy of MSC transplantation, on prevention of esophageal damage and stricture formation after caustic esophagus injury in rats. 54 rats were allocated into four groups; 4 rats were sacrificed for MSC production. Group 1, untreated controls (n: 10). Group 2, membrane labeled MSCs-treated rats (n: 20). Group 3, biodistribution of fluorodeoxyglucose labeled MSCs via positron emission tomography (PET) imaging (n: 10). Group 4, sham operated (n: 10). Standard caustic esophageal burns were created and MSCs were transplanted 24 hours after. All rats were sacrificed at the 21st days. Results. PET scan images revealed the homing behavior of MSCs to the injury site. The histopathology damage score was not significantly different from controls. However, we demonstrated Dil labeled epithelial and muscle cells which were originating from transplanted MSCs. Conclusion. MSC transplantation after caustic esophageal injury may be a helpful treatment modality; however, probably repeated infusions are needed.
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spelling pubmed-40270182014-05-29 The Efficacy of Mesenchymal Stem Cell Transplantation in Caustic Esophagus Injury: An Experimental Study Kantarcioglu, Murat Caliskan, Bahadir Demirci, Hakan Karacalioglu, Ozgur Kekilli, Murat Polat, Zulfikar Gunal, Armagan Akinci, Melih Uysal, Cagri Eksert, Sami Gurel, Hasan Celebi, Gurkan Avcu, Ferit Ural, Ali Ugur Bagci, Sait Stem Cells Int Research Article Introduction. Ingestion of corrosive substances may lead to stricture formation in esophagus as a late complication. Full thickness injury seems to exterminate tissue stem cells of esophagus. Mesenchymal stem cells (MSCs) can differentiate into specific cell lineages and have the capacity of homing in sites of injury. Aim and Methods. We aimed to investigate the efficacy of MSC transplantation, on prevention of esophageal damage and stricture formation after caustic esophagus injury in rats. 54 rats were allocated into four groups; 4 rats were sacrificed for MSC production. Group 1, untreated controls (n: 10). Group 2, membrane labeled MSCs-treated rats (n: 20). Group 3, biodistribution of fluorodeoxyglucose labeled MSCs via positron emission tomography (PET) imaging (n: 10). Group 4, sham operated (n: 10). Standard caustic esophageal burns were created and MSCs were transplanted 24 hours after. All rats were sacrificed at the 21st days. Results. PET scan images revealed the homing behavior of MSCs to the injury site. The histopathology damage score was not significantly different from controls. However, we demonstrated Dil labeled epithelial and muscle cells which were originating from transplanted MSCs. Conclusion. MSC transplantation after caustic esophageal injury may be a helpful treatment modality; however, probably repeated infusions are needed. Hindawi Publishing Corporation 2014 2014-05-04 /pmc/articles/PMC4027018/ /pubmed/24876849 http://dx.doi.org/10.1155/2014/939674 Text en Copyright © 2014 Murat Kantarcioglu et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Kantarcioglu, Murat
Caliskan, Bahadir
Demirci, Hakan
Karacalioglu, Ozgur
Kekilli, Murat
Polat, Zulfikar
Gunal, Armagan
Akinci, Melih
Uysal, Cagri
Eksert, Sami
Gurel, Hasan
Celebi, Gurkan
Avcu, Ferit
Ural, Ali Ugur
Bagci, Sait
The Efficacy of Mesenchymal Stem Cell Transplantation in Caustic Esophagus Injury: An Experimental Study
title The Efficacy of Mesenchymal Stem Cell Transplantation in Caustic Esophagus Injury: An Experimental Study
title_full The Efficacy of Mesenchymal Stem Cell Transplantation in Caustic Esophagus Injury: An Experimental Study
title_fullStr The Efficacy of Mesenchymal Stem Cell Transplantation in Caustic Esophagus Injury: An Experimental Study
title_full_unstemmed The Efficacy of Mesenchymal Stem Cell Transplantation in Caustic Esophagus Injury: An Experimental Study
title_short The Efficacy of Mesenchymal Stem Cell Transplantation in Caustic Esophagus Injury: An Experimental Study
title_sort efficacy of mesenchymal stem cell transplantation in caustic esophagus injury: an experimental study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4027018/
https://www.ncbi.nlm.nih.gov/pubmed/24876849
http://dx.doi.org/10.1155/2014/939674
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