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Mesenchymal stem cells: a future experimental exploration for recession of diabetic nephropathy

Background: The progresses made in stem cell therapy offer an innovative approach and exhibit great potential for the repair of damaged organs and tissues. This study was conducted with a view to find the mechanisms responsible for the effectiveness of bone marrow-derived mesenchymal stem cells (BM-...

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Autores principales: Hamza, Amal H., Al-Bishri, Widad M, Damiati, Laila A., Ahmed, Hanaa H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6014323/
https://www.ncbi.nlm.nih.gov/pubmed/27774826
http://dx.doi.org/10.1080/0886022X.2016.1244080
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author Hamza, Amal H.
Al-Bishri, Widad M
Damiati, Laila A.
Ahmed, Hanaa H.
author_facet Hamza, Amal H.
Al-Bishri, Widad M
Damiati, Laila A.
Ahmed, Hanaa H.
author_sort Hamza, Amal H.
collection PubMed
description Background: The progresses made in stem cell therapy offer an innovative approach and exhibit great potential for the repair of damaged organs and tissues. This study was conducted with a view to find the mechanisms responsible for the effectiveness of bone marrow-derived mesenchymal stem cells (BM-MSCs) in the suppression of diabetes and experimentally-induced diabetic nephropathy. Methods: To realize this objective, diabetic and diabetic nephropathy subject groups that underwent MSC treatment were studied through numerous biochemistry and molecular genetics analyses. Results: The findings show that, relative to the control groups, the rats in the diabetic and diabetic nephropathy groups treated with stem cells infused with BM-MSCs showed a significant reversal in the levels of their insulin, glucose, heme-oxygenase-1 (HO-1) serum, and advanced glycation end product (AGEP). Moreover, BM-MSC therapy was also found to have a definite positive effect on the kidney functions. In addition, it also corresponded with a significant decrease in the availability of certain growth factors, namely the fibroblast growth factor (FGF), the platelet-derived growth factor (PDGF), and the transforming growth factor-β (TGF-β). BM-MSC treatment also improved the levels of expression of monocyte chemoatractant-1 (MCP-1) and interleukin-8 (IL-8) genes within kidney tissues. Lastly, the treatment recovered the organizational structure of the kidney and pancreas, a result demonstrated by a histopathological analysis. These results greatly coincide with those obtained through the biochemistry and molecular genetics analyses. Conclusion: Treatment using BM-MSCs is determined to be definitely effective in cases of diabetes and diabetic nephropathy.
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spelling pubmed-60143232018-06-28 Mesenchymal stem cells: a future experimental exploration for recession of diabetic nephropathy Hamza, Amal H. Al-Bishri, Widad M Damiati, Laila A. Ahmed, Hanaa H. Ren Fail Laboratory Study Background: The progresses made in stem cell therapy offer an innovative approach and exhibit great potential for the repair of damaged organs and tissues. This study was conducted with a view to find the mechanisms responsible for the effectiveness of bone marrow-derived mesenchymal stem cells (BM-MSCs) in the suppression of diabetes and experimentally-induced diabetic nephropathy. Methods: To realize this objective, diabetic and diabetic nephropathy subject groups that underwent MSC treatment were studied through numerous biochemistry and molecular genetics analyses. Results: The findings show that, relative to the control groups, the rats in the diabetic and diabetic nephropathy groups treated with stem cells infused with BM-MSCs showed a significant reversal in the levels of their insulin, glucose, heme-oxygenase-1 (HO-1) serum, and advanced glycation end product (AGEP). Moreover, BM-MSC therapy was also found to have a definite positive effect on the kidney functions. In addition, it also corresponded with a significant decrease in the availability of certain growth factors, namely the fibroblast growth factor (FGF), the platelet-derived growth factor (PDGF), and the transforming growth factor-β (TGF-β). BM-MSC treatment also improved the levels of expression of monocyte chemoatractant-1 (MCP-1) and interleukin-8 (IL-8) genes within kidney tissues. Lastly, the treatment recovered the organizational structure of the kidney and pancreas, a result demonstrated by a histopathological analysis. These results greatly coincide with those obtained through the biochemistry and molecular genetics analyses. Conclusion: Treatment using BM-MSCs is determined to be definitely effective in cases of diabetes and diabetic nephropathy. Taylor & Francis 2016-10-23 /pmc/articles/PMC6014323/ /pubmed/27774826 http://dx.doi.org/10.1080/0886022X.2016.1244080 Text en © 2016 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group 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 work is properly cited.
spellingShingle Laboratory Study
Hamza, Amal H.
Al-Bishri, Widad M
Damiati, Laila A.
Ahmed, Hanaa H.
Mesenchymal stem cells: a future experimental exploration for recession of diabetic nephropathy
title Mesenchymal stem cells: a future experimental exploration for recession of diabetic nephropathy
title_full Mesenchymal stem cells: a future experimental exploration for recession of diabetic nephropathy
title_fullStr Mesenchymal stem cells: a future experimental exploration for recession of diabetic nephropathy
title_full_unstemmed Mesenchymal stem cells: a future experimental exploration for recession of diabetic nephropathy
title_short Mesenchymal stem cells: a future experimental exploration for recession of diabetic nephropathy
title_sort mesenchymal stem cells: a future experimental exploration for recession of diabetic nephropathy
topic Laboratory Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6014323/
https://www.ncbi.nlm.nih.gov/pubmed/27774826
http://dx.doi.org/10.1080/0886022X.2016.1244080
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