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Pharmacological Inhibition of Gal-3 in Mesenchymal Stem Cells Enhances Their Capacity to Promote Alternative Activation of Macrophages in Dextran Sulphate Sodium-Induced Colitis

Transplantation of mesenchymal stem cells (MSCs) reduces the severity of dextran sulphate sodium- (DSS-) induced colitis. MSCs are able to secrete Galectin-3 (Gal-3), a protein known to affect proliferation, adhesion, and migration of immune cells. We investigate whether newly synthetized inhibitor...

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Autores principales: Simovic Markovic, Bojana, Nikolic, Aleksandar, Gazdic, Marina, Nurkovic, Jasmin, Djordjevic, Irena, Arsenijevic, Nebojsa, Stojkovic, Miodrag, Lukic, Miodrag L., Volarevic, Vladislav
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4736319/
https://www.ncbi.nlm.nih.gov/pubmed/27057168
http://dx.doi.org/10.1155/2016/2640746
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author Simovic Markovic, Bojana
Nikolic, Aleksandar
Gazdic, Marina
Nurkovic, Jasmin
Djordjevic, Irena
Arsenijevic, Nebojsa
Stojkovic, Miodrag
Lukic, Miodrag L.
Volarevic, Vladislav
author_facet Simovic Markovic, Bojana
Nikolic, Aleksandar
Gazdic, Marina
Nurkovic, Jasmin
Djordjevic, Irena
Arsenijevic, Nebojsa
Stojkovic, Miodrag
Lukic, Miodrag L.
Volarevic, Vladislav
author_sort Simovic Markovic, Bojana
collection PubMed
description Transplantation of mesenchymal stem cells (MSCs) reduces the severity of dextran sulphate sodium- (DSS-) induced colitis. MSCs are able to secrete Galectin-3 (Gal-3), a protein known to affect proliferation, adhesion, and migration of immune cells. We investigate whether newly synthetized inhibitor of Gal-3 (Davanat) will affect production of Gal-3 in MSCs and enhance their potential to attenuate DSS-induced colitis. Pharmacological inhibition of Gal-3 in MSCs enhances their capacity to promote alternative activation of peritoneal macrophages in vitro and in vivo. Injection of MSCs cultured in the presence of Davanat increased concentration of IL-10 in sera of DSS-treated animals and markedly enhanced presence of alternatively activated and IL-10 producing macrophages in the colons of DSS-treated mice. Pharmacological inhibition of Gal-3 in MSCs significantly attenuates concentration of Gal-3 in sera of DSS-treated animals, indicating that MSCs produce Gal-3 in this disease. In conclusion, our findings indicate that Davanat could be used for improvement of MSC-mediated polarization towards immunosuppressive M2 phenotype of macrophages.
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spelling pubmed-47363192016-04-07 Pharmacological Inhibition of Gal-3 in Mesenchymal Stem Cells Enhances Their Capacity to Promote Alternative Activation of Macrophages in Dextran Sulphate Sodium-Induced Colitis Simovic Markovic, Bojana Nikolic, Aleksandar Gazdic, Marina Nurkovic, Jasmin Djordjevic, Irena Arsenijevic, Nebojsa Stojkovic, Miodrag Lukic, Miodrag L. Volarevic, Vladislav Stem Cells Int Research Article Transplantation of mesenchymal stem cells (MSCs) reduces the severity of dextran sulphate sodium- (DSS-) induced colitis. MSCs are able to secrete Galectin-3 (Gal-3), a protein known to affect proliferation, adhesion, and migration of immune cells. We investigate whether newly synthetized inhibitor of Gal-3 (Davanat) will affect production of Gal-3 in MSCs and enhance their potential to attenuate DSS-induced colitis. Pharmacological inhibition of Gal-3 in MSCs enhances their capacity to promote alternative activation of peritoneal macrophages in vitro and in vivo. Injection of MSCs cultured in the presence of Davanat increased concentration of IL-10 in sera of DSS-treated animals and markedly enhanced presence of alternatively activated and IL-10 producing macrophages in the colons of DSS-treated mice. Pharmacological inhibition of Gal-3 in MSCs significantly attenuates concentration of Gal-3 in sera of DSS-treated animals, indicating that MSCs produce Gal-3 in this disease. In conclusion, our findings indicate that Davanat could be used for improvement of MSC-mediated polarization towards immunosuppressive M2 phenotype of macrophages. Hindawi Publishing Corporation 2016 2016-01-04 /pmc/articles/PMC4736319/ /pubmed/27057168 http://dx.doi.org/10.1155/2016/2640746 Text en Copyright © 2016 Bojana Simovic Markovic et al. https://creativecommons.org/licenses/by/4.0/ 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
Simovic Markovic, Bojana
Nikolic, Aleksandar
Gazdic, Marina
Nurkovic, Jasmin
Djordjevic, Irena
Arsenijevic, Nebojsa
Stojkovic, Miodrag
Lukic, Miodrag L.
Volarevic, Vladislav
Pharmacological Inhibition of Gal-3 in Mesenchymal Stem Cells Enhances Their Capacity to Promote Alternative Activation of Macrophages in Dextran Sulphate Sodium-Induced Colitis
title Pharmacological Inhibition of Gal-3 in Mesenchymal Stem Cells Enhances Their Capacity to Promote Alternative Activation of Macrophages in Dextran Sulphate Sodium-Induced Colitis
title_full Pharmacological Inhibition of Gal-3 in Mesenchymal Stem Cells Enhances Their Capacity to Promote Alternative Activation of Macrophages in Dextran Sulphate Sodium-Induced Colitis
title_fullStr Pharmacological Inhibition of Gal-3 in Mesenchymal Stem Cells Enhances Their Capacity to Promote Alternative Activation of Macrophages in Dextran Sulphate Sodium-Induced Colitis
title_full_unstemmed Pharmacological Inhibition of Gal-3 in Mesenchymal Stem Cells Enhances Their Capacity to Promote Alternative Activation of Macrophages in Dextran Sulphate Sodium-Induced Colitis
title_short Pharmacological Inhibition of Gal-3 in Mesenchymal Stem Cells Enhances Their Capacity to Promote Alternative Activation of Macrophages in Dextran Sulphate Sodium-Induced Colitis
title_sort pharmacological inhibition of gal-3 in mesenchymal stem cells enhances their capacity to promote alternative activation of macrophages in dextran sulphate sodium-induced colitis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4736319/
https://www.ncbi.nlm.nih.gov/pubmed/27057168
http://dx.doi.org/10.1155/2016/2640746
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